Sunday, 8 April 2012

Iron Suspension


Pronunciation: EYE-urn
Generic Name: Iron
Brand Name: Icar


Iron Suspension is used for:

Supplementing iron in the diet and treating or preventing anemia (low red blood cell levels) due to low iron levels. It may also be used for other conditions as determined by your doctor.


Iron Suspension is a mineral. It works by helping the body to make hemoglobin, which is found in red blood cells. Hemoglobin allows red blood cells to carry oxygen throughout the body, which helps to reduce the effects of anemia.


Do NOT use Iron Suspension if:


  • you are allergic to any ingredient in Iron Suspension

  • you have high levels of iron in the blood

Contact your doctor or health care provider right away if any of these apply to you.



Before using Iron Suspension:


Some medical conditions may interact with Iron Suspension. Tell your doctor or pharmacist if you have any medical conditions, especially if any of the following apply to you:


  • if you are pregnant, planning to become pregnant, or are breast-feeding

  • if you are taking any prescription or nonprescription medicine, herbal preparation, or dietary supplement

  • if you have allergies to medicines, foods, or other substances

  • if you have colon problems, Crohn disease, or a peptic ulcer

  • if you have anemia not caused by iron deficiency, porphyria cutanea tarda, liver or kidney problems, thalassemia, or a history of alcohol abuse, or you have had multiple blood transfusions

Some MEDICINES MAY INTERACT with Iron Suspension. However, no specific interactions with Iron Suspension are known at this time.


This may not be a complete list of all interactions that may occur. Ask your health care provider if Iron Suspension may interact with other medicines that you take. Check with your health care provider before you start, stop, or change the dose of any medicine.


How to use Iron Suspension:


Use Iron Suspension as directed by your doctor. Check the label on the medicine for exact dosing instructions.


  • Iron Suspension is absorbed better on an empty stomach, but may be taken with food if it upsets your stomach.

  • Shake well before using.

  • Use a measuring device marked for medicine dosing. Ask your pharmacist for help if you are unsure of how to measure your dose.

  • Do not take antacids within 1 hour before or 2 hours after taking Iron Suspension.

  • Take Iron Suspension with a full glass (8 oz/240 mL) of water.

  • Do not lie down for 30 minutes after taking Iron Suspension.

  • If you miss a dose of Iron Suspension, take it as soon as possible. If it is almost time for your next dose, skip the missed dose and go back to your regular dosing schedule. Do not take 2 doses at once.

Ask your health care provider any questions you may have about how to use Iron Suspension.



Important safety information:


  • Do not take large doses of vitamins (megadoses or megavitamin therapy) unless otherwise instructed by your doctor.

  • Accidental overdose of iron-containing products is a leading cause of fatal poisoning in children younger than 6 years of age. In case of accidental overdose, call a doctor or poison control center immediately.

  • Some of these products contain sulfites, which can cause allergic reactions in certain individuals (eg, asthma patients). If you have previously had allergic reactions to sulfites, contact your pharmacist to determine if the product you are taking contains sulfites.

  • Some of these products may contain tartrazine dye (FD&C Yellow No. 5), which can cause allergic reactions in certain patients. If you have previously had an allergic reaction to tartrazine, contact your pharmacist to determine if the medicine you are taking contains tartrazine.

  • Iron Suspension may cause incorrect test results with kits used to check for blood in the stool or blood cholesterol. Check with your doctor if you are using either kind of test kit.

  • LAB TESTS, including blood cell counts, may be performed to monitor your progress or to check for side effects. Be sure to keep all doctor and lab appointments.

  • PREGNANCY and BREAST-FEEDING: If you become pregnant, discuss with your doctor the benefits and risks of using Iron Suspension during pregnancy. If you are or will be breast-feeding while you are using Iron Suspension, check with your doctor or pharmacist to discuss the risks to your baby.


Possible side effects of Iron Suspension:


All medicines may cause side effects, but many people have no, or minor, side effects. Check with your doctor if any of these most COMMON side effects persist or become bothersome:



Constipation; diarrhea; nausea; stomach discomfort.



Seek medical attention right away if any of these SEVERE side effects occur:

Severe allergic reactions (rash; hives; itching; difficulty breathing; tightness in the chest; swelling of the mouth, face, lips, or tongue); black, tarry stools; blood or streaks of blood in the stool; fever; sharp stomach pain; vomiting.



This is not a complete list of all side effects that may occur. If you have questions about side effects, contact your health care provider. Call your doctor for medical advice about side effects. To report side effects to the appropriate agency, please read the Guide to Reporting Problems to FDA.


See also: Iron side effects (in more detail)


If OVERDOSE is suspected:


Contact 1-800-222-1222 (the American Association of Poison Control Centers), your local poison control center, or emergency room immediately. Accidental overdose of iron-containing products is a leading cause of fatal poisoning in children younger than 6 years of age. In case of accidental overdose, call a doctor or poison control center immediately. Symptoms may include loss of consciousness; nausea; seizures; stomach pain; tarry stools; tiredness; vomiting; weak, fast heartbeat.


Proper storage of Iron Suspension:

Store Iron Suspension at room temperature, between 59 and 86 degrees F (15 and 30 degrees C). Store away from heat, moisture, and light. Keep Iron Suspension out of the reach of children and away from pets.


General information:


  • If you have any questions about Iron Suspension, please talk with your doctor, pharmacist, or other health care provider.

  • Iron Suspension is to be used only by the patient for whom it is prescribed. Do not share it with other people.

  • If your symptoms do not improve or if they become worse, check with your doctor.

  • Check with your pharmacist about how to dispose of unused medicine.

This information is a summary only. It does not contain all information about Iron Suspension. If you have questions about the medicine you are taking or would like more information, check with your doctor, pharmacist, or other health care provider.



Issue Date: February 1, 2012

Database Edition 12.1.1.002

Copyright © 2012 Wolters Kluwer Health, Inc.

More Iron resources


  • Iron Side Effects (in more detail)
  • Iron Use in Pregnancy & Breastfeeding
  • Iron Drug Interactions
  • Iron Support Group
  • 0 Reviews for Iron - Add your own review/rating


Compare Iron with other medications


  • Iron Deficiency Anemia

Estradiol Gel Packets



Pronunciation: ES-tra-DYE-ol
Generic Name: Estradiol
Brand Name: Divigel

Estradiol Gel Packets should not be used to prevent heart disease, heart attacks, strokes, or dementia. Estrogens have been shown to increase the risk of heart disease (including heart attack), stroke, dementia, serious blood clots (eg, in the lungs or legs), cancer of the uterus, and breast cancer in some women. Tell your doctor right away if you have unusual vaginal bleeding while you use Estradiol Gel Packets. Talk with your doctor if you have questions about the benefits and risks of using Estradiol Gel Packets.


Estradiol Gel Packets should be used for the shortest possible time at the lowest effective dose to minimize the risk of these side effects. Talk with your doctor regularly about your need to use Estradiol Gel Packets.





Estradiol Gel Packets are used for:

Treating certain moderate to severe symptoms of menopause (eg, hot flashes).


Estradiol Gel Packets are an estrogen hormone. It works by replacing estrogen in the body when it no longer produces enough on its own.


Do NOT use Estradiol Gel Packets if:


  • you are allergic to any ingredient in Estradiol Gel Packets

  • you are pregnant or suspect you may be pregnant

  • you have undiagnosed abnormal vaginal bleeding

  • you have a history of blood clots (eg, in the lungs, legs, eyes); endometrial, cervical, or vaginal cancer; estrogen-dependent growths; breast cancer; or liver problems

  • you have had a heart attack or stroke within the past 12 months

Contact your doctor or health care provider right away if any of these apply to you.



Before using Estradiol Gel Packets:


Some medical conditions may interact with Estradiol Gel Packets. Tell your doctor or pharmacist if you have any medical conditions, especially if any of the following apply to you:


  • if you are pregnant, planning to become pregnant, or are breast-feeding

  • if you are taking any prescription or nonprescription medicine, herbal preparation, or dietary supplement

  • if you have allergies to medicines, foods, or other substances

  • if you have a history of endometriosis, growths in the uterus, abnormal mammogram, abnormal vaginal bleeding, a lump in the breast, or fibrocystic breast disease, or if a family member has had breast cancer

  • if you have dementia or other memory problems, or abnormal blood calcium levels

  • if you have a history of asthma, cancer, high blood cholesterol or lipid levels, diabetes, heart problems, high blood pressure, heart attack or stroke, kidney problems, liver tumor, mental or mood problems (eg, depression), underactive thyroid, migraine headaches, gallbladder or pancreas problems, seizures (eg, epilepsy), lupus, chorea, or the blood disease porphyria

  • if you smoke, are very overweight, or will be having surgery

  • if you have a history of yellowing of the eyes or skin during pregnancy or with past estrogen use

  • if a member of your family has a history of blood clots (eg, in the legs, lungs, eyes), diabetes, lupus, or obesity

  • if you have had your uterus removed (hysterectomy)

Some MEDICINES MAY INTERACT with Estradiol Gel Packets. Tell your health care provider if you are taking any other medicines, especially any of the following:


  • Azole antifungals (eg, ketoconazole), HIV protease inhibitors (eg, ritonavir), or macrolide antibiotics (eg, erythromycin) because they may increase the risk of Estradiol Gel Packets's side effects

  • Barbiturates (eg, phenobarbital), carbamazepine, hydantoins (eg, phenytoin), rifampin, or St. John's wort because they may decrease Estradiol Gel Packets's effectiveness

  • Thyroid hormones (eg, levothyroxine) because their effectiveness may be decreased by Estradiol Gel Packets

This may not be a complete list of all interactions that may occur. Ask your health care provider if Estradiol Gel Packets may interact with other medicines that you take. Check with your health care provider before you start, stop, or change the dose of any medicine.


How to use Estradiol Gel Packets:


Use Estradiol Gel Packets as directed by your doctor. Check the label on the medicine for exact dosing instructions.


  • An extra patient leaflet is available with Estradiol Gel Packets. Talk to your pharmacist if you have questions about this information.

  • Apply Estradiol Gel Packets to the upper thigh area of the right or left leg. Change between your left and right thigh each day to help avoid skin irritation.

  • Apply Estradiol Gel Packets to clean, intact skin only. Be sure the area is completely dry before applying Estradiol Gel Packets.

  • Do not apply Estradiol Gel Packets to skin that is irritated or broken. Do not apply it to your face, in or around the vagina, or to your breasts.

  • If you take a bath or shower, or use a sauna around the time of your dose, apply Estradiol Gel Packets afterwards. Be sure the area is completely dry before applying the medicine.

  • Open the packet and squeeze the entire contents of the packet onto the upper thigh of one leg. Gently spread the medicine as thinly as possible over an area of about 5 to 7 inches (about 2 palm prints). You do not need to rub the medicine in.

  • Throw away the empty packet in the trash out of the reach of children and pets.

  • Wash your hands with soap and water after using Estradiol Gel Packets.

  • Cover the application site with clothing after the medicine is completely dry. This will help to prevent others from coming into contact with the medicine. Be sure the medicine is completely dry before you dress.

  • Do not wash the application site for at least 1 hour after you apply Estradiol Gel Packets.

  • Do not allow others to apply Estradiol Gel Packets for you. Do not allow others to come into contact with the application site for at least 1 hour after you apply Estradiol Gel Packets. If someone else comes into contact with Estradiol Gel Packets, have them wash the area with soap and water right away.

  • Use Estradiol Gel Packets at the same time each day.

  • If you spill some of Estradiol Gel Packets while you are applying it, do not open a new packet. Wait and apply your regular dose the next day.

  • If you miss a dose of Estradiol Gel Packets, use it as soon as possible. If your next dose is less than 12 hours away, skip the missed dose and go back to your regular dosing schedule. Do not use 2 doses at once.

Ask your health care provider any questions you may have about how to use Estradiol Gel Packets.



Important safety information:


  • Estradiol Gel Packets are for external use only. Do not get it in your eyes, nose, vagina, or mouth. If you get it in any of these areas, rinse right away with warm clean water.

  • Check with your doctor before applying sunscreen to the application site while using Estradiol Gel Packets.

  • If you will be swimming, wait until Estradiol Gel Packets are completely dry before going into the water.

  • Estradiol Gel Packets are flammable. Avoid fire, flame, or smoking until the medicine has dried on your skin.

  • Eating grapefruit or drinking grapefruit juice may increase the risk of Estradiol Gel Packets's side effects. Talk to your doctor before including grapefruit or grapefruit juice in your diet while you are taking Estradiol Gel Packets.

  • Tell your doctor or dentist that you take Estradiol Gel Packets before you receive any medical or dental care, emergency care, or surgery. If possible, Estradiol Gel Packets should be stopped at least 4 to 6 weeks before surgery or any time you might be confined to a bed or chair for a long period of time (such as a long plane flight, car ride, bedrest, or illness).

  • Estradiol Gel Packets may cause dark skin patches on your face. Exposure to the sun may make these patches darker. If patches develop, use a sunscreen or wear protective clothing when exposed to the sun, sunlamps, or tanning booths.

  • If you wear contact lenses and you develop problems with them, contact your doctor.

  • Diabetes patients - Estradiol Gel Packets may affect your blood sugar. Check blood sugar levels closely. Ask your doctor before you change the dose of your diabetes medicine.

  • Estradiol Gel Packets may interfere with certain lab tests. Be sure your doctor and lab personnel know you are using Estradiol Gel Packets.

  • Lab tests and medical exams, including breast exams, mammograms, Pap tests, physicals, and blood pressure, may be performed while you use Estradiol Gel Packets. These tests may be used to monitor your condition or check for side effects. Be sure to keep all doctor and lab appointments.

  • Examine your breasts monthly as directed by your doctor. Report any lumps right away.

  • Estradiol Gel Packets should not be used in CHILDREN; safety and effectiveness in children have not been confirmed.

  • PREGNANCY and BREAST-FEEDING: Do not use Estradiol Gel Packets if you are pregnant. If you think you may be pregnant, contact your doctor right away. Estradiol Gel Packets are found in breast milk. If you are or will be breast-feeding while you use Estradiol Gel Packets, check with your doctor. Discuss any possible risks to your baby.


Possible side effects of Estradiol Gel Packets:


All medicines may cause side effects, but many people have no, or minor, side effects. Check with your doctor if any of these most COMMON side effects persist or become bothersome:



Breast pain or tenderness; headache; mild hair loss; mild nausea or vomiting; spotting or breakthrough bleeding; stomach cramps or bloating.



Seek medical attention right away if any of these SEVERE side effects occur:

Severe allergic reactions (rash; hives; itching; difficulty breathing; tightness in the chest; swelling of the mouth, face, lips, or tongue; unusual hoarseness); blurred or double vision, vision loss, or other vision changes; breast lump or discharge; calf or leg pain or swelling; chest pain; confusion; coughing up blood; fainting; memory problems; mental or mood changes (eg, depression); migraine headache; numbness of an arm or leg; one-sided weakness; persistent or recurring abnormal vaginal bleeding; severe or persistent headache or dizziness; severe or persistent stomach pain, nausea, or vomiting; shortness of breath; slurred speech; swelling of the hands, legs, or feet; vaginal discharge, itching, or odor; yellowing of the skin or eyes.



This is not a complete list of all side effects that may occur. If you have questions about side effects, contact your health care provider. Call your doctor for medical advice about side effects. To report side effects to the appropriate agency, please read the Guide to Reporting Problems to FDA.



If OVERDOSE is suspected:


Contact 1-800-222-1222 (the American Association of Poison Control Centers), your local poison control center, or emergency room immediately. Symptoms may include abnormal vaginal bleeding; or severe or persistent nausea or vomiting.


Proper storage of Estradiol Gel Packets:

Store Estradiol Gel Packets at room temperature, between 68 and 77 degrees F (20 and 25 degrees C) with the cap secured. Brief storage at temperatures between 59 and 86 degrees F (15 and 30 degrees C) is permitted. Store away from heat, moisture, and light. Do not store in the bathroom. Keep Estradiol Gel Packets out of the reach of children and away from pets.


General information:


  • If you have any questions about Estradiol Gel Packets, please talk with your doctor, pharmacist, or other health care provider.

  • Estradiol Gel Packets are to be used only by the patient for whom it is prescribed. Do not share it with other people.

  • If your symptoms do not improve or if they become worse, check with your doctor.

  • Check with your pharmacist about how to dispose of unused medicine.

This information is a summary only. It does not contain all information about Estradiol Gel Packets. If you have questions about the medicine you are taking or would like more information, check with your doctor, pharmacist, or other health care provider.



Issue Date: February 1, 2012

Database Edition 12.1.1.002

Copyright © 2012 Wolters Kluwer Health, Inc.

More Estradiol resources


  • Estradiol Use in Pregnancy & Breastfeeding
  • Drug Images
  • Estradiol Drug Interactions
  • Estradiol Support Group
  • 57 Reviews for Estradiol - Add your own review/rating


Compare Estradiol with other medications


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Somatropin (rDNA origin - Refrigerated) Cartridge


Pronunciation: SOE-ma-TROE-pin
Generic Name: Somatropin (rDNA origin - Refrigerated)
Brand Name: Humatrope


Somatropin (rDNA origin - Refrigerated) Cartridge is used for:

Treating certain children or adults when the body does not produce enough growth hormone. It is also used to treat certain children who are not growing normally because of Turner syndrome or certain other conditions (eg, idiopathic short stature, short stature homeobox-containing gene [SHOX] deficiency). It may also be used for other conditions as determined by your doctor.


Somatropin (rDNA origin - Refrigerated) Cartridge is a growth hormone. It works by stimulating growth in patients who do not make enough natural growth hormone.


Do NOT use Somatropin (rDNA origin - Refrigerated) Cartridge if:


  • you are allergic to any ingredient in Somatropin (rDNA origin - Refrigerated) Cartridge or in the diluent, including metacresol or glycerin

  • you have active or recurring cancer or brain tumor, or you currently receive treatment for cancer

  • you have severe breathing problems (eg, respiratory failure) or a serious illness caused by complications from a surgery or injury

  • you have a certain type of eye problem caused by diabetes (diabetic retinopathy)

  • the patient is a child who has Prader-Willi syndrome and is severely overweight or has severe breathing problems (eg, respiratory infection, history of airway blockage or sleep apnea)

  • the patient is a child who has epiphyseal closure (bone growth is complete)

Contact your doctor or health care provider right away if any of these apply to you.



Before using Somatropin (rDNA origin - Refrigerated) Cartridge:


Some medical conditions may interact with Somatropin (rDNA origin - Refrigerated) Cartridge. Tell your doctor or pharmacist if you have any medical conditions, especially if any of the following apply to you:


  • if you are pregnant, planning to become pregnant, or are breast-feeding

  • if you are taking any prescription or nonprescription medicine, herbal preparation, or dietary supplement

  • if you have allergies to medicines, foods, or other substances

  • if you have a history of kidney or liver problems, lung or breathing problems (eg, airway blockage, respiratory infection, sleep apnea), an underactive thyroid, heart problems, high blood pressure, ear or hearing problems (eg, repeated ear infections), pancreas problems, or endocrine problems (eg, pituitary or adrenal gland problems)

  • if you have a history of diabetes or high blood sugar levels, or if a member of your family has had diabetes

  • if you have a history of leukemia, other types of cancer (eg, skin cancer), or any unusual growths or tumors (especially in the brain)

  • if you have curvature of the spine (scoliosis), Prader-Willi syndrome, or a certain eye problem called papilledema (swelling of the area around your optic nerve)

  • if you are very overweight or have had a recent major surgery or injury

Some MEDICINES MAY INTERACT with Somatropin (rDNA origin - Refrigerated) Cartridge. Tell your health care provider if you are taking any other medicines, especially any of the following:


  • Corticosteroids (eg, prednisone) or estrogens because they may decrease Somatropin (rDNA origin - Refrigerated) Cartridge's effectiveness

  • Anticonvulsants (eg, carbamazepine) or cyclosporine because the risk of their side effects may be increased by Somatropin (rDNA origin - Refrigerated) Cartridge

  • Insulin or other medicines for diabetes because their effectiveness may be decreased by Somatropin (rDNA origin - Refrigerated) Cartridge

This may not be a complete list of all interactions that may occur. Ask your health care provider if Somatropin (rDNA origin - Refrigerated) Cartridge may interact with other medicines that you take. Check with your health care provider before you start, stop, or change the dose of any medicine.


How to use Somatropin (rDNA origin - Refrigerated) Cartridge:


Use Somatropin (rDNA origin - Refrigerated) Cartridge as directed by your doctor. Check the label on the medicine for exact dosing instructions.


  • An extra patient leaflet is available with Somatropin (rDNA origin - Refrigerated) Cartridge. Talk to your pharmacist if you have questions about this information.

  • Somatropin (rDNA origin - Refrigerated) Cartridge is given as an injection under the skin. A health care provider will teach you how to use it. Be sure you understand how to use Somatropin (rDNA origin - Refrigerated) Cartridge. Follow the procedures you are taught when you use a dose. Contact your health care provider if you have any questions.

  • Somatropin (rDNA origin - Refrigerated) Cartridge should only be used with a certain kind of pen device. Ask your health care provider if you have any questions.

  • Do NOT shake Somatropin (rDNA origin - Refrigerated) Cartridge. Swirl gently to mix.

  • Somatropin (rDNA origin - Refrigerated) Cartridge should be clear and colorless. Do not use Somatropin (rDNA origin - Refrigerated) Cartridge if it contains particles, is cloudy or discolored, or if the container is cracked or damaged.

  • Be sure to rotate your injection site as directed to help avoid thickening or hardening of the skin.

  • Keep this product, as well as syringes and needles, out of the reach of children and pets. Do not reuse needles, syringes, or other materials. Ask your health care provider how to dispose of these materials after use. Follow all local rules for disposal.

  • If you miss a dose of Somatropin (rDNA origin - Refrigerated) Cartridge, use it as soon as possible. If it is almost time for your next dose, skip the missed dose and go back to your regular dosing schedule. Do not use 2 doses at once.

Ask your health care provider any questions you may have about how to use Somatropin (rDNA origin - Refrigerated) Cartridge.



Important safety information:


  • Severe and sometimes fatal lung and breathing problems have occurred with the use of Somatropin (rDNA origin - Refrigerated) Cartridge in certain children with Prader-Willi syndrome. These children were usually either very overweight or had severe breathing problems (eg, airway blockage, sleep apnea, lung or airway infection). The risk may be greater in boys. Children with Prader-Willi syndrome should have certain breathing tests before they start Somatropin (rDNA origin - Refrigerated) Cartridge. They should be monitored for signs of lung or airway infection. They should also have effective weight control. Contact the doctor at once if the patient develops irregular breathing during sleep, new or increased snoring, or symptoms of lung or airway infection (eg, fever, coughing, sore throat, shortness of breath, chest pain or discomfort).

  • Rarely, children using Somatropin (rDNA origin - Refrigerated) Cartridge have experienced a slipped growth plate in the hip. Contact the doctor right away if the patient develops hip or knee pain or a limp.

  • Rarely, increased blood pressure in the head has been reported in patients using somatropin. The risk may be greater in patients with Turner syndrome or Prader-Willi syndrome. Symptoms usually occurred within the first 8 weeks after the start of treatment. The symptoms have gone away after the dose was lowered or treatment was stopped. Discuss any questions or concerns with your doctor. Contact your doctor right away if you develop symptoms such as vision changes or severe headache, nausea, or vomiting.

  • Pancreas inflammation (pancreatitis) has been reported rarely in patients who take Somatropin (rDNA origin - Refrigerated) Cartridge. The risk may be greater in children, especially in girls who have Turner syndrome. Contact your doctor right away if you develop stomach or back pain.

  • Somatropin (rDNA origin - Refrigerated) Cartridge may raise your blood sugar. High blood sugar may make you feel confused, drowsy, or thirsty. It can also make you flush, breathe faster, or have a fruit-like breath odor. If these symptoms occur, tell your doctor right away.

  • Diabetes patients - Somatropin (rDNA origin - Refrigerated) Cartridge may affect your blood sugar. Check blood sugar levels closely. Ask your doctor before you change the dose of your diabetes medicine.

  • Lab tests, including blood sugar levels, eye exams, and thyroid function, may be performed while you use Somatropin (rDNA origin - Refrigerated) Cartridge. These tests may be used to monitor your condition or check for side effects. Be sure to keep all doctor and lab appointments.

  • Use Somatropin (rDNA origin - Refrigerated) Cartridge with caution in the ELDERLY; they may be more sensitive to its effects.

  • Caution is advised when using Somatropin (rDNA origin - Refrigerated) Cartridge in CHILDREN; they may be more sensitive to its effects, especially pancreas inflammation.

  • PREGNANCY and BREAST-FEEDING: If you become pregnant, contact your doctor. You will need to discuss the benefits and risks of using Somatropin (rDNA origin - Refrigerated) Cartridge while you are pregnant. It is not known if Somatropin (rDNA origin - Refrigerated) Cartridge is found in breast milk. If you are or will be breast-feeding while you use Somatropin (rDNA origin - Refrigerated) Cartridge, check with your doctor. Discuss any possible risks to your baby.


Possible side effects of Somatropin (rDNA origin - Refrigerated) Cartridge:


All medicines may cause side effects, but many people have no, or minor, side effects. Check with your doctor if any of these most COMMON side effects persist or become bothersome:



Back pain; headache; increased cough; mild flu-like symptoms; mild swelling (eg, of the hands or feet); muscle or joint pain; redness or itching at the injection site; sore throat; stuffy or runny nose.



Seek medical attention right away if any of these SEVERE side effects occur:

Severe allergic reactions (rash; hives; itching; difficulty breathing; tightness in the chest; swelling of the mouth, face, lips, or tongue); breast enlargement in males; burning, tingling, or numbness; change in appearance or size of a mole; chest pain or discomfort; confusion; ear pain, discharge, or discomfort; fever; hearing problems; hip or knee pain; limp; nausea or vomiting; new growth on the skin; one-sided weakness; persistent or severe cough or sore throat; severe or persistent muscle or joint pain; severe or persistent stomach or back pain; severe or persistent swelling of the hands, ankles, or feet; shortness of breath; slurred speech; snoring or irregular breathing during sleep; sudden, severe, or persistent headache or dizziness; symptoms of high blood sugar (eg, increased thirst, hunger, or urination; unusual weakness); thickened or hardened skin at the injection site; trouble breathing; unusual bruising; vision changes.



This is not a complete list of all side effects that may occur. If you have questions about side effects, contact your health care provider. Call your doctor for medical advice about side effects. To report side effects to the appropriate agency, please read the Guide to Reporting Problems to FDA.


See also: Somatropin (rDNA origin - Refrigerated) side effects (in more detail)


If OVERDOSE is suspected:


Contact 1-800-222-1222 (the American Association of Poison Control Centers), your local poison control center, or emergency room immediately. Symptoms may include swelling of the hands, ankles, or feet; symptoms of high or low blood sugar (eg, dizziness; fainting; fast breathing; fast heartbeat; flushing; increased sweating; increased thirst, hunger, or urination; vision changes; unusual weakness).


Proper storage of Somatropin (rDNA origin - Refrigerated) Cartridge:

Store new (unopened) cartridges in the refrigerator, between 36 and 46 degrees F (2 and 8 degrees C). Do not freeze. Protect from light. Do not use Somatropin (rDNA origin - Refrigerated) Cartridge past the expiration date on the product label.


After mixing, store cartridges in the refrigerator, between 36 and 46 degrees F (2 and 8 degrees C). Do not freeze. Store without the needle attached. Throw away cartridges after 28 days, even if they still contain medicine.


Contact your pharmacist if you have any questions about how to properly store Somatropin (rDNA origin - Refrigerated) Cartridge. Keep Somatropin (rDNA origin - Refrigerated) Cartridge out of the reach of children and away from pets.


General information:


  • If you have any questions about Somatropin (rDNA origin - Refrigerated) Cartridge, please talk with your doctor, pharmacist, or other health care provider.

  • Somatropin (rDNA origin - Refrigerated) Cartridge is to be used only by the patient for whom it is prescribed. Do not share it with other people.

  • If your symptoms do not improve or if they become worse, check with your doctor.

  • Check with your pharmacist about how to dispose of unused medicine.

This information is a summary only. It does not contain all information about Somatropin (rDNA origin - Refrigerated) Cartridge. If you have questions about the medicine you are taking or would like more information, check with your doctor, pharmacist, or other health care provider.



Issue Date: February 1, 2012

Database Edition 12.1.1.002

Copyright © 2012 Wolters Kluwer Health, Inc.

More Somatropin (rDNA origin - Refrigerated) resources


  • Somatropin (rDNA origin - Refrigerated) Side Effects (in more detail)
  • Somatropin (rDNA origin - Refrigerated) Use in Pregnancy & Breastfeeding
  • Somatropin (rDNA origin - Refrigerated) Drug Interactions
  • Somatropin (rDNA origin - Refrigerated) Support Group
  • 13 Reviews for Somatropin (rDNA origin - Refrigerated) - Add your own review/rating


Compare Somatropin (rDNA origin - Refrigerated) with other medications


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Monday, 2 April 2012

Ophthalmic preparations


Ophthalmic preparations are agents especially designed to be applied to the eyes. The eye is extremely sensitive and is easily irritated if the composition of the ophthalmic preparation is not appropriate.

See also

  • anti-angiogenic ophthalmic agents
  • miscellaneous ophthalmic agents
  • mydriatics
  • ophthalmic anesthetics
  • ophthalmic anti-infectives
  • ophthalmic anti-inflammatory agents
  • ophthalmic antihistamines and decongestants
  • ophthalmic diagnostic agents
  • ophthalmic glaucoma agents
  • ophthalmic lubricants and irrigations
  • ophthalmic steroids
  • ophthalmic steroids with anti-infectives
  • ophthalmic surgical agents

Drug List:

Salicylic Acid Cream


Pronunciation: sal-ih-SILL-ik AS-id
Generic Name: Salicylic Acid
Brand Name: Examples include Fostex and Stridex Body Focus


Salicylic Acid Cream is used for:

Treating acne. It may also be used for other conditions as determined by your doctor.


Salicylic Acid Cream is a topical salicylate. It works by causing the skin to swell, soften, and then slough or peel in areas where it is applied.


Do NOT use Salicylic Acid Cream if:


  • you are allergic to any ingredient in Salicylic Acid Cream

Contact your doctor or health care provider right away if any of these apply to you.



Before using Salicylic Acid Cream:


Some medical conditions may interact with Salicylic Acid Cream. Tell your doctor or pharmacist if you have any medical conditions, especially if any of the following apply to you:


  • if you are pregnant, planning to become pregnant, or are breast-feeding

  • if you are taking any prescription or nonprescription medicine, herbal preparation, or dietary supplement

  • if you have allergies to medicines, foods, or other substances

  • if you have had a severe allergic reaction (eg, severe rash, hives, difficulty breathing, dizziness) to aspirin or a nonsteroidal anti-inflammatory drug (NSAID) (eg, ibuprofen, naproxen, celecoxib)

  • if you have liver or kidney problems, a skin infection, skin irritation, diabetes, or poor blood circulation

Some MEDICINES MAY INTERACT with Salicylic Acid Cream. Tell your health care provider if you are taking any other medicines, especially any of the following:


  • Anticoagulants, (eg, heparin, warfarin), aspirin, methotrexate, or sulfonylureas (eg, glipizide) because the risk of side effects may be increased by Salicylic Acid Cream

This may not be a complete list of all interactions that may occur. Ask your health care provider if Salicylic Acid Cream may interact with other medicines that you take. Check with your health care provider before you start, stop, or change the dose of any medicine.


How to use Salicylic Acid Cream:


Use Salicylic Acid Cream as directed by your doctor. Check the label on the medicine for exact dosing instructions.


  • Wash and thoroughly dry the affected area. Apply a thin layer of Salicylic Acid Cream to cover the entire affected area. Gently rub the medicine in until it is evenly distributed. Unless your hands are being treated, be sure to wash your hands after each use.

  • If you miss a dose of Salicylic Acid Cream, use it as soon as possible. If it is almost time for your next dose, skip the missed dose and go back to your regular dosing schedule. Do not use 2 doses at once.

Ask your health care provider any questions you may have about how to use Salicylic Acid Cream.



Important safety information:


  • Salicylic Acid Cream is for external use only. Avoid getting Salicylic Acid Cream in your eyes, nose, or mouth, or on the genitals. If contact with your eyes occurs, flush with water for 15 minutes. Do not inhale the vapors of Salicylic Acid Cream.

  • Overuse of topical products may worsen your condition.

  • Do not use Salicylic Acid Cream longer or more often than recommended by your doctor or on the package label.

  • Check with your doctor before use if you have a condition that covers a large area of the body.

  • Be sure to apply Salicylic Acid Cream only to the affected area and not to normal healthy skin.

  • Do not use Salicylic Acid Cream on skin that is irritated, infected, or reddened.

  • Do not use Salicylic Acid Cream on open skin wounds, moles, birthmarks, genital warts, warts on the face, or warts growing hair.

  • Do not use any other medicines or drying products on your skin unless your doctor instructs you otherwise.

  • Salicylic Acid Cream may interfere with certain lab test results. Make sure your doctor and lab personnel know you are using Salicylic Acid Cream.

  • Salicylic Acid Cream is extremely flammable. Do not store or use Salicylic Acid Cream near a fire or other open flame.

  • Salicylic Acid Cream may be harmful if swallowed. If you may have taken Salicylic Acid Cream by mouth, contact your local poison control center or emergency room immediately.

  • Salicylic Acid Cream contains a salicylate, which has been linked to Reye syndrome. Do not use Salicylic Acid Cream on children or teenagers during or after chickenpox, flu, or other viral infections without checking with your doctor or pharmacist.

  • Caution is advised when using Salicylic Acid Cream in CHILDREN because they may be more sensitive to its effects.

  • PREGNANCY and BREAST-FEEDING: If you become pregnant, discuss with your doctor the benefits and risks of using Salicylic Acid Cream during pregnancy. It is unknown if Salicylic Acid Cream is excreted in breast milk. Do not breast-feed while you are using Salicylic Acid Cream.


Possible side effects of Salicylic Acid Cream:


All medicines may cause side effects, but many people have no, or minor, side effects. Check with your doctor if any of these most COMMON side effects persist or become bothersome:



Dry, peeling, red, or scaling skin.



Seek medical attention right away if any of these SEVERE side effects occur:

Severe allergic reactions (rash; hives; itching; difficulty breathing; tightness in the chest; swelling of the mouth, face, lips, or tongue); severe irritation.



This is not a complete list of all side effects that may occur. If you have questions about side effects, contact your health care provider. Call your doctor for medical advice about side effects. To report side effects to the appropriate agency, please read the Guide to Reporting Problems to FDA.


See also: Salicylic Acid side effects (in more detail)


If OVERDOSE is suspected:


Contact 1-800-222-1222 (the American Association of Poison Control Centers), your local poison control center, or emergency room immediately. Symptoms may include agitation; diarrhea; dizziness; loss of appetite; loss of hearing; mental disturbances; nausea; rapid or difficult breathing; ringing in the ears; seizures; sluggishness; vomiting; yellowing of the skin or eyes.


Proper storage of Salicylic Acid Cream:

Store Salicylic Acid Cream at room temperature, between 68 and 77 degrees F (20 and 25 degrees C). Store away from heat, moisture, and light. Do not freeze. Do not store in the bathroom. Keep Salicylic Acid Cream out of the reach of children and away from pets.


General information:


  • If you have any questions about Salicylic Acid Cream, please talk with your doctor, pharmacist, or other health care provider.

  • Salicylic Acid Cream is to be used only by the patient for whom it is prescribed. Do not share it with other people.

  • If your symptoms do not improve or if they become worse, check with your doctor.

  • Check with your pharmacist about how to dispose of unused medicine.

This information is a summary only. It does not contain all information about Salicylic Acid Cream. If you have questions about the medicine you are taking or would like more information, check with your doctor, pharmacist, or other health care provider.



Issue Date: February 1, 2012

Database Edition 12.1.1.002

Copyright © 2012 Wolters Kluwer Health, Inc.

More Salicylic Acid resources


  • Salicylic Acid Side Effects (in more detail)
  • Salicylic Acid Use in Pregnancy & Breastfeeding
  • Salicylic Acid Drug Interactions
  • Salicylic Acid Support Group
  • 1 Review for Salicylic Acid - Add your own review/rating


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  • Acne
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ceftriaxone


Generic Name: ceftriaxone (SEF trye AX one)

Brand names: Rocephin, Rocephin IM Convenience Kit (obsolete), Rocephin ADD-Vantage


What is ceftriaxone injection?

Ceftriaxone is in a group of drugs called cephalosporin (SEF a low spor in) antibiotics. It works by fighting bacteria in your body.


Ceftriaxone injection is used to treat many kinds of bacterial infections, including severe or life-threatening forms such as meningitis.


Ceftriaxone may also be used for purposes other than those listed in this medication guide.


What is the most important information I should know about ceftriaxone injection?


Do not use this medication if you are allergic to ceftriaxone, or to similar antibiotics, such as Ceftin, Cefzil, Keflex, Omnicef, and others.

Before using this medication, tell your doctor if you are allergic to any drugs (especially penicillin). Also tell your doctor if you have liver or kidney disease, gallbladder problems, a stomach or intestinal disorder, or if you are malnourished.


Use this medication for the entire length of time prescribed by your doctor. Your symptoms may get better before the infection is completely treated. Ceftriaxone is usually continued for at least 2 days after symptoms disappear.


Ceftriaxone will not treat a viral infection such as the common cold or flu.


Antibiotic medicines can cause diarrhea, which may be a sign of a new infection. If you have diarrhea that is watery or has blood in it, call your doctor. Do not use any medicine to stop the diarrhea unless your doctor has told you to.


What should I discuss with my health care provider before using ceftriaxone injection?


Do not use this medication if you are allergic to ceftriaxone, or to other cephalosporin antibiotics, such as:

  • cefaclor (Raniclor);




  • cefadroxil (Duricef);




  • cefazolin (Ancef);




  • cefdinir (Omnicef);




  • cefditoren (Spectracef);




  • cefpodoxime (Vantin);




  • cefprozil (Cefzil);




  • ceftibuten (Cedax);




  • cefuroxime (Ceftin);




  • cephalexin (Keflex); or




  • cephradine (Velosef).



If you have certain conditions, you may need a dose adjustment or special tests to safely use this medication. Before using ceftriaxone, tell your doctor if you are allergic to any drugs (especially penicillins), or if you have:


  • kidney disease (or if you are on dialysis);

  • liver disease;


  • gallbladder problems;




  • a stomach or intestinal disorder such as colitis; or




  • if you are malnourished.




FDA pregnancy category B. This medication is not expected to be harmful to an unborn baby. Tell your doctor if you are pregnant or plan to become pregnant during treatment. Ceftriaxone can pass into breast milk and may harm a nursing baby. Do not use this medication without telling your doctor if you are breast-feeding a baby. Do not use ceftriaxone in a child without a doctor's advice, and never give more than the child's prescribed dose.

How should I use ceftriaxone injection?


Ceftriaxone is given as an injection into a muscle or a vein. Your doctor, nurse, or other healthcare provider will give you this injection. You may be given instructions on how to use your injections at home. Do not use this medicine at home if you do not fully understand how to give the injection and properly dispose of needles, syringes, and other items used in giving the medicine.


Use the medication exactly as it was prescribed for you. Do not use it in larger amounts or use it for longer than recommended by your doctor. Follow the instructions on your prescription label.


You will need to mix ceftriaxone with a liquid (diluent) before using it. If you are using the injections at home, be sure you understand how to properly mix and store the medication. Use only the diluent your doctor has recommended.


Do not mix ceftriaxone with any diluent that contains calcium, including a TPN (total parenteral nutrition) solution.

Use this medication for the entire length of time prescribed by your doctor. Your symptoms may get better before the infection is completely treated. Ceftriaxone is usually continued for at least 2 days after symptoms disappear.


Ceftriaxone will not treat a viral infection such as the common cold or flu.


Store this medicine at room temperature, away from moisture, heat, and light.

If your medicine was provided in a frozen form or was frozen after mixing, thaw it in a refrigerator or at room temperature. Do not warm in a microwave or boiling water. Use the medicine as soon as possible after thawing it. Do not refreeze.


What happens if I miss a dose?


Use the medication as soon as you remember the missed dose. If it is almost time for your next dose, skip the missed dose and use the medicine at your next regularly scheduled time. Do not use extra medicine to make up the missed dose.


What happens if I overdose?


Seek emergency medical attention if you think you have used too much of this medicine.

What should I avoid while using ceftriaxone injection?


Antibiotic medicines can cause diarrhea, which may be a sign of a new infection. If you have diarrhea that is watery or has blood in it, call your doctor. Do not use any medicine to stop the diarrhea unless your doctor has told you to.


Ceftriaxone injection side effects


Get emergency medical help if you have any of these signs of an allergic reaction: hives; difficulty breathing; swelling of your face, lips, tongue, or throat. Call your doctor at once if you have any of these serious side effects:

  • diarrhea that is watery or bloody;




  • fever or chills;




  • skin rash, bruising, severe tingling, numbness, pain, muscle weakness;




  • blistering, peeling, and red skin rash;




  • white patches or sores inside your mouth or on your lips;




  • pale or yellowed skin, dark colored urine, confusion or weakness;




  • urinating less than usual or not at all;




  • swelling, pain, or irritation where the injection was given; or




  • chalky-colored stools, stomach pain just after eating a meal, nausea, heartburn, bloating, and severe upper stomach pain that may spread to your back.



Less serious side effects may include:



  • nausea, vomiting, stomach pain;




  • headache, dizziness;




  • pain or swelling in your tongue;




  • sweating; or




  • vaginal itching or discharge.



This is not a complete list of side effects and others may occur. Call your doctor for medical advice about side effects. You may report side effects to FDA at 1-800-FDA-1088.


Ceftriaxone Dosing Information


Usual Adult Dose for Bacterial Infection:

Usual daily dose: 1 to 2 g/day IV or IM in 1 to 2 divided doses, depending on the nature and severity of the infection

For infections caused by Staphylococcus aureus (methicillin-susceptible, MSSA), the recommended dose is 2 to 4 g/day, in order to achieve greater than 90% target attainment.

The total daily dose should not exceed 4 g.

Usual Adult Dose for Bacteremia:

2 g IV every 24 hours for 14 days, depending on the nature and severity of the infection

Usual Adult Dose for Chancroid:

250 mg IM as a single dose

The causative organism is Haemophilus ducreyi.

HIV-infected patients may require longer treatment. Ceftriaxone should only be given if patient follow-up can be guaranteed.

Patients should be retested for syphilis and HIV in 3 months, if initial tests were negative. The patient's sexual partner(s) should also be evaluated/treated.

Usual Adult Dose for Conjunctivitis:

Gonococcal Conjunctivitis: 1 g IM once

Doxycycline therapy for 7 days (if not pregnant) or single dose azithromycin is also recommended to treat possible concurrent chlamydial infection.

The patient's sexual partner(s) should also be evaluated/treated.

Usual Adult Dose for Endocarditis:

Patients with normal renal function:

Native valve infections due to highly penicillin-susceptible viridans Group Streptococci and S bovis (MIC 0.12 mcg/mL or less): Ceftriaxone 2 g IV or IM every 24 hours for 4 weeks plus gentamicin 3 mg/kg IV or IM every 24 hours for 2 weeks

Native valve infections due to relatively resistant S viridans and S bovis (MIC greater than 0.12 mcg/mL and 0.5 mcg/mL or less): Ceftriaxone 2 g IV or IM every 24 hours for 4 weeks plus gentamicin 3 mg/kg IV or IM every 24 hours for 2 weeks

Prosthetic valve infections due to penicillin-susceptible S viridans and S bovis (MIC 0.12 mcg/mL or less): Ceftriaxone 2 g IV or IM every 24 hours for 6 weeks plus gentamicin 3 mg/kg IV or IM every 24 hours for 2 weeks

Prosthetic valve infections due to relatively or fully penicillin-resistant S viridans and S bovis (MIC greater than 0.12 mcg/mL): Ceftriaxone 2 g IV or IM every 24 hours for 6 weeks plus gentamicin 3 mg/kg IV or IM every 24 hours for 6 weeks

Native or prosthetic valve infections due to enterococcal strains resistant to penicillin, aminoglycosides, and vancomycin: Ceftriaxone 2 g IV or IM every 24 hours plus ampicillin 2 g IV every 4 hours for 8 weeks or more

Gonococcal endocarditis: 1 to 2 g IV every 12 hours for at least 4 weeks

Refer to current published guidelines for detailed recommendations.

Usual Adult Dose for Bacterial Endocarditis Prophylaxis:

As an alternative in patients unable to take oral medication, with or without penicillin allergy (non-anaphylactoid type): 1 g IV or IM once 30 to 60 minutes before procedure

Usual Adult Dose for Endometritis:

2 g IV every 24 hours plus clindamycin

Duration: Parenteral therapy should be continued for at least 24 hours after the patient has remained afebrile, pain free, and the leukocyte count has normalized. Doxycycline therapy for 14 days is recommended if concurrent chlamydial infection is present in late postpartum patients (breast-feeding should be discontinued).

Usual Adult Dose for Epididymitis -- Sexually Transmitted:

Gonococcal epididymitis: 250 mg IM as a single dose

Doxycycline 100 mg twice daily orally for 10 days should be given to treat a concurrent chlamydial infection.

The patient's sexual partner(s) should also be evaluated/treated.

Usual Adult Dose for Epiglottitis:

2 g IV every 24 hours for 7 to 10 days, depending on the nature and severity of the infection

Usual Adult Dose for Gastroenteritis:

2 g IV every 24 hours
Duration: 7 to 10 days in immunocompromised patients

Usual Adult Dose for Gonococcal Infection -- Disseminated:

1 g IV or IM every 24 hours

Duration: Parenteral therapy should be continued for 24 to 48 hours after clinical improvement is demonstrated. Oral therapy with cefixime should then be continued to complete a total course of at least 1 week.

Doxycycline therapy for 7 days (if not pregnant) or single dose azithromycin is also recommended to treat possible concurrent chlamydial infection.

The patient's sexual partner(s) should also be evaluated/treated.

Usual Adult Dose for Gonococcal Infection -- Uncomplicated:

Uncomplicated infections of the cervix, urethra, rectum, or pharynx: 250 mg IM once

Doxycycline therapy for 7 days (if not pregnant) or single dose azithromycin is also recommended to treat possible concurrent chlamydial infection.

The patient's sexual partner(s) should also be evaluated/treated.

Usual Adult Dose for Intraabdominal Infection:

2 g IV every 24 hours for 7 to 14 days, depending on the nature and severity of the infection

Usual Adult Dose for Joint Infection:

1 to 2 g IV or IM every 24 hours

Duration: 3 to 4 weeks, depending on the nature and severity of the infection; longer therapy, 6 weeks or more, may be required for prosthetic joint infections

Usual Adult Dose for Lyme Disease -- Arthritis:

2 g IV or IM every 24 hours

Febrile patients should also be evaluated/treated for human granulocytic ehrlichiosis (HGE) and babesiosis.

Duration: 14 days for arthritis, up to 21 days for carditis, and up to 30 days for neurologic Lyme disease

Usual Adult Dose for Lyme Disease -- Carditis:

2 g IV or IM every 24 hours

Febrile patients should also be evaluated/treated for human granulocytic ehrlichiosis (HGE) and babesiosis.

Duration: 14 days for arthritis, up to 21 days for carditis, and up to 30 days for neurologic Lyme disease

Usual Adult Dose for Lyme Disease -- Neurologic:

2 g IV or IM every 24 hours

Febrile patients should also be evaluated/treated for human granulocytic ehrlichiosis (HGE) and babesiosis.

Duration: 14 days for arthritis, up to 21 days for carditis, and up to 30 days for neurologic Lyme disease

Usual Adult Dose for Meningitis:

2 g IV every 12 hours for 14 days, depending on the nature and severity of the infection

Gonococcal meningitis: 1 to 2 g IV every 12 hours for 10 to 14 days

Usual Adult Dose for Meningococcal Meningitis Prophylaxis:

250 mg IM once

Usual Adult Dose for Neurosyphilis:

2 g IV or IM every 24 hours for 10 to 14 days

Aqueous crystalline penicillin G is considered the drug of choice by the CDC.

The patient's sexual partner(s) should also be evaluated/treated.

Usual Adult Dose for Osteomyelitis:

1 to 2 g IV or IM every 24 hours

Duration: 4 to 6 weeks, depending on the nature and severity of the infection; additional oral antibiotic therapy may be required for up to 6 months for chronic osteomyelitis

Usual Adult Dose for Pelvic Inflammatory Disease:

Outpatient treatment of mild PID: 250 mg IM once plus oral doxycycline with or without metronidazole
Severe: 1 to 2 g IV or IM every 24 hours for 14 days, depending on the nature and severity of the infection

Doxycycline therapy for 14 days (if not pregnant) is also recommended to treat possible concurrent chlamydial infection.

The patient's sexual partner(s) should also be evaluated/treated.

Usual Adult Dose for Peritonitis:

2 g IV every 24 hours

Peritoneal dialysis-related peritonitis:
Continuous: 1 g/2 L dialysate intraperitoneally, followed by 250 to 500 mg/2 L dialysate
Intermittent: 1 g/2 L dialysate intraperitoneally every 24 hours

Duration: 10 to 14 days, depending on the nature and severity of the infection

Usual Adult Dose for Pneumonia:

1 to 2 g IV or IM every 24 hours for 7 to 21 days, depending on the nature and severity of the infection

Usual Adult Dose for Prostatitis:

Gonococcal prostatitis: 250 mg IM once

Doxycycline 100 mg twice daily orally for 10 days should be given to treat a concurrent chlamydial infection.

The patient's sexual partner(s) should also be evaluated/treated.

Usual Adult Dose for Pyelonephritis:

1 to 2 g IV or IM every 24 hours
Duration: 14 days, depending on the nature and severity of the infection

Usual Adult Dose for Salmonella Gastroenteritis:

2 g IV every 24 hours
Duration: Up to 14 days in immunocompromised patients, or longer if a relapse occurs

Usual Adult Dose for Sepsis:

Severe: 2 g IV every 24 hours for 14 days, depending on the nature and severity of the infection

Usual Adult Dose for Skin or Soft Tissue Infection:

Severe: 1 to 2 g IV or IM every 24 hours

Duration: 7 to 10 days, depending on the nature and severity of the infection; diabetic soft tissue infections may require treatment for 14 to 21 days

Usual Adult Dose for STD Prophylaxis:

STD prophylaxis, sexual assault: 250 mg IM once, in combination with metronidazole and azithromycin or doxycycline
Sexual partner(s) of patients with chancroid: 250 mg IM once

Usual Adult Dose for Surgical Prophylaxis:

1 g IV once 30 to 120 minutes before surgery
Third generation cephalosporins are generally not recommended for routine surgical prophylaxis.

Usual Adult Dose for Syphilis -- Early:

1 g IV or IM every 24 hours for 10 to 14 days

Benzathine penicillin G is considered the drug of choice by the CDC.

The patient's sexual partner(s) should also be evaluated/treated.

Usual Adult Dose for Typhoid Fever:

2 g IV every 24 hours

Duration: 7 to 10 days; if the patient is immunocompromised or a relapse occurs, 14 days or more of treatment may be required

Usual Adult Dose for Urinary Tract Infection:

Severe: 1 to 2 g IV or IM every 24 hours
Duration: 2 to 3 weeks for complicated infections

Usual Pediatric Dose for Bacterial Infection:

Less than 1 week: 50 mg/kg IV or IM every 24 hours
1 to 4 weeks, 2000 g or less: 50 mg/kg IV or IM every 24 hours
1 to 4 weeks, greater than 2000 g: 50 to 75 mg/kg IV or IM every 24 hours

Ceftriaxone should be avoided in neonates with hyperbilirubinemia.

1 month or older:
Severe: 50 to 75 mg/kg IV in divided doses every 12 to 24 hours (maximum dose: 2 g/24 hours)
Life-threatening: 80 to 100 mg/kg IV in 1 or 2 divided doses (maximum dose: 4 g/24 hours)

Usual Pediatric Dose for Gonococcal Infection -- Uncomplicated:

Infants of mothers with gonococcal infection (gonococcal prophylaxis): 25 to 50 mg/kg (maximum dose: 125 mg) IV or IM once

Ceftriaxone should be avoided in neonates with hyperbilirubinemia.

Infant and mother should be evaluated/treated for possible concurrent chlamydial infection. The mother's sexual partner(s) should also be evaluated/treated.

Children with uncomplicated infections of the vulva and vagina, cervix, urethra, rectum, or pharynx:
45 kg or less: 125 mg IM once
Greater than 45 kg: 250 mg IM once

Patients should be evaluated/treated for possible concurrent syphilis and/or chlamydial infections.

Usual Pediatric Dose for Gonococcal Infection -- Disseminated:

0 to 4 weeks: 25 to 50 mg/kg (maximum dose: 125 mg) IV or IM every 24 hours for 7 days, up to 10 to 14 days if meningitis is documented

Ceftriaxone should be avoided in neonates with hyperbilirubinemia.

1 month or older:
45 kg or less:
Arthritis or bacteremia: 50 mg/kg (maximum dose: 1 g) IV or IM every 24 hours for 7 days

Greater than 45 kg: 1 g IV or IM once a day for 7 days

Patients should be evaluated/treated for possible concurrent syphilis and/or chlamydial infections.

Usual Pediatric Dose for Meningitis:

0 to 4 weeks: 50 to 75 mg/kg every 24 hours

Ceftriaxone should be avoided in neonates with hyperbilirubinemia.

1 month or older:
Initial dose: 100 mg/kg IV at the start of therapy (maximum dose: 4 g)
Maintenance dose: 100 mg/kg/day IV once a day or in divided doses every 12 hours for 7 to 14 days (maximum dose: 4 g/24 hours)

Gonococcal infection:
45 kg or less: 50 mg/kg/day IV or IM divided every 12 hours for 10 to 14 days (maximum dose: 2 g/day)
Greater than 45 kg: 1 to 2 g IV or IM every 12 hours for 10 to 14 days

Usual Pediatric Dose for Meningococcal Meningitis Prophylaxis:

Less than 15 years: 125 mg IM once
15 years or older: 250 mg IM once

Usual Pediatric Dose for Endocarditis:

Gonococcal infection:
45 kg or less: 50 mg/kg/day IV or IM divided every 12 hours for at least 28 days (maximum dose: 2 g/day)
Greater than 45 kg: 1 to 2 g IV or IM every 12 hours for at least 28 days

Usual Pediatric Dose for Bacterial Endocarditis Prophylaxis:

As an alternative in patients unable to take oral medication, with or without penicillin allergy (non-anaphylactoid type): 50 mg/kg (maximum dose: 1 g) IV or IM once 30 to 60 minutes before procedure

Usual Pediatric Dose for Otitis Media:

Acute bacterial otitis media: 50 mg/kg IM once (maximum dose: 1 g)
Persistent or relapsing acute otitis media: 50 mg/kg IV or IM once a day for 3 days (maximum dose: 1 g/day)

Ceftriaxone should be avoided in neonates with hyperbilirubinemia.

Usual Pediatric Dose for Epiglottitis:

1 month or older: 50 to 100 mg/kg IV or IM once a day
Duration: Has been reported to range from 2 to 14 days

Usual Pediatric Dose for Skin and Structure Infection:

1 month or older: 50 to 75 mg/kg/day IV or IM in 1 to 2 divided doses (maximum dose: 2 g/day)

Usual Pediatric Dose for Typhoid Fever:

1 month or older: 75 to 80 mg/kg IV once a day for 5 to 14 days

Usual Pediatric Dose for Lyme Disease:

Persistent arthritis, meningitis, encephalitis: 75 to 100 mg/kg/day (maximum dose: 2 g) IV or IM for 2 to 4 weeks

Usual Pediatric Dose for Salmonella Gastroenteritis:

50 to 75 mg/kg/day IV for 2 to 5 days

Treat immunocompromised patients for up to 10 days.

Ceftriaxone should be avoided in neonates with hyperbilirubinemia.

Usual Pediatric Dose for Shigellosis:

50 to 75 mg/kg/day IV for 2 to 5 days

Treat immunocompromised patients for up to 10 days.

Ceftriaxone should be avoided in neonates with hyperbilirubinemia.

Usual Pediatric Dose for STD Prophylaxis:

STD prophylaxis, sexual assault:
13 years or older: 250 mg IM once, in combination with metronidazole and azithromycin or doxycycline

Usual Pediatric Dose for Conjunctivitis:

Gonococcal infection:
Neonates: 25 to 50 mg/kg (maximum dose: 125 mg) IV or IM once

1 month or older:
45 kg or less: 50 mg/kg (maximum dose: 1 g) IV or IM once
Greater than 45 kg: 1 g IM once

Usual Pediatric Dose for Chancroid:

1 month or older: 50 mg/kg (maximum dose: 250 mg) IM as a single dose

Usual Pediatric Dose for Epididymitis -- Non-Specific:

250 mg IM as a single dose


What other drugs will affect ceftriaxone injection?


There may be other drugs that can interact with ceftriaxone. Tell your doctor about all the prescription and over-the-counter medications you use. This includes vitamins, minerals, herbal products, and drugs prescribed by other doctors. Do not start using a new medication without telling your doctor.



More ceftriaxone resources


  • Ceftriaxone Side Effects (in more detail)
  • Ceftriaxone Use in Pregnancy & Breastfeeding
  • Ceftriaxone Drug Interactions
  • Ceftriaxone Support Group
  • 23 Reviews for Ceftriaxone - Add your own review/rating


  • ceftriaxone Injection Advanced Consumer (Micromedex) - Includes Dosage Information

  • Ceftriaxone Prescribing Information (FDA)

  • Ceftriaxone MedFacts Consumer Leaflet (Wolters Kluwer)

  • Ceftriaxone Sodium Monograph (AHFS DI)

  • Rocephin Prescribing Information (FDA)

  • Rocephin Consumer Overview



Compare ceftriaxone with other medications


  • Bacteremia
  • Bacterial Endocarditis Prevention
  • Bacterial Infection
  • Bone infection
  • Chancroid
  • Conjunctivitis
  • Endocarditis
  • Endometritis
  • Epididymitis, Non-Specific
  • Epididymitis, Sexually Transmitted
  • Epiglottitis
  • Gastroenteritis
  • Gonococcal Infection, Disseminated
  • Gonococcal Infection, Uncomplicated
  • Intraabdominal Infection
  • Joint Infection
  • Kidney Infections
  • Lyme Disease
  • Lyme Disease, Arthritis
  • Lyme Disease, Carditis
  • Lyme Disease, Neurologic
  • Meningitis
  • Meningococcal Meningitis Prophylaxis
  • Neurosyphilis
  • Otitis Media
  • Pelvic Inflammatory Disease
  • Peritonitis
  • Pneumonia
  • Prostatitis
  • Salmonella Gastroenteritis
  • Sepsis
  • Shigellosis
  • Skin and Structure Infection
  • Skin Infection
  • STD Prophylaxis
  • Surgical Prophylaxis
  • Syphilis, Early
  • Typhoid Fever
  • Urinary Tract Infection


Where can I get more information?


  • Your doctor or pharmacist can provide more information about ceftriaxone.

See also: ceftriaxone side effects (in more detail)


Ipol


Generic Name: poliovirus vaccine, inactivated (Injection route)


POE-lee-oh VYE-rus VAX-een, in-AK-ti-vated


Commonly used brand name(s)

In the U.S.


  • Ipol

Available Dosage Forms:


  • Injectable

  • Suspension

Therapeutic Class: Vaccine


Uses For Ipol


Poliovirus vaccine is an active immunizing agent used to prevent poliomyelitis (polio). It works by causing your body to produce its own protection (antibodies) against the virus that causes polio.


There are two types of polio vaccine that are given by injection, poliovirus vaccine inactivated (IPV) and poliovirus vaccine inactivated enhanced potency (eIPV). In the U.S. and Canada, the type of vaccine that is given by injection is eIPV. The type of vaccine that is given by mouth is called poliovirus vaccine live oral (OPV).


Polio is a very serious infection that causes paralysis of the muscles, including the muscles that enable you to walk and breathe. A polio infection may leave a person unable to breathe without the help of an iron lung, unable to walk without leg braces, or confined to a wheelchair. There is no cure for polio.


Immunization against polio is recommended for all infants from 6 to 12 weeks of age, all children, all adolescents up to 18 years of age, and certain adults who are at greater risk for exposure to polioviruses than the general population, including:


  • Persons traveling to areas or countries where polio is uncontrolled, whether or not they have been vaccinated against polio in the past.

  • Persons who live in areas where polio infection still occurs.

  • Adults who have not been vaccinated or who have not had the complete series of vaccinations against polio and who live in households with children who are to be given the oral polio vaccine (OPV).

  • Employees in day-care centers and group homes for children, such as orphanages.

  • Employees in medical facilities, such as hospitals and doctors' offices.

  • Laboratory workers handling samples that may contain polio viruses.

Immunization against polio is not recommended for infants younger than 6 weeks of age, because antibodies they received from their mothers before birth may interfere with the effectiveness of the vaccine. Infants who were immunized against polio before 6 weeks of age should receive the complete polio immunization series.


This vaccine is to be administered only by or under the supervision of your doctor or other health care professional.


Before Using Ipol


In deciding to use a vaccine, the risks of taking the vaccine must be weighed against the good it will do. This is a decision you and your doctor will make. For this vaccine, the following should be considered:


For a while after you are immunized, there is a very small risk (1 in 2.2 million) that any persons living in your household who have not yet been immunized against polio or who have or had an immune deficiency condition may develop poliomyelitis (polio) from being around you. Talk to your doctor if you have any questions about this.


Allergies


Tell your doctor if you have ever had any unusual or allergic reaction to this medicine or any other medicines. Also tell your health care professional if you have any other types of allergies, such as to foods, dyes, preservatives, or animals. For non-prescription products, read the label or package ingredients carefully.


Pediatric


Use is not recommended for infants up to 6 weeks of age. For infants and children 6 weeks of age and older, polio vaccine is not expected to cause different side effects or problems than it does in adults.


Geriatric


Many medicines have not been studied specifically in older people. Therefore, it may not be known whether they work exactly the same way they do in younger adults. Although there is no specific information comparing use of polio vaccine in the elderly with use in other age groups, this vaccine is not expected to cause different side effects or problems in older persons than it does in younger adults.


Pregnancy








Pregnancy CategoryExplanation
All TrimestersCAnimal studies have shown an adverse effect and there are no adequate studies in pregnant women OR no animal studies have been conducted and there are no adequate studies in pregnant women.

Breast Feeding


Studies in women suggest that this medication poses minimal risk to the infant when used during breastfeeding.


Interactions with Medicines


Although certain medicines should not be used together at all, in other cases two different medicines may be used together even if an interaction might occur. In these cases, your doctor may want to change the dose, or other precautions may be necessary. Tell your healthcare professional if you are taking any other prescription or nonprescription (over-the-counter [OTC]) medicine.


Interactions with Food/Tobacco/Alcohol


Certain medicines should not be used at or around the time of eating food or eating certain types of food since interactions may occur. Using alcohol or tobacco with certain medicines may also cause interactions to occur. Discuss with your healthcare professional the use of your medicine with food, alcohol, or tobacco.


Other Medical Problems


The presence of other medical problems may affect the use of this vaccine. Make sure you tell your doctor if you have any other medical problems, especially:


  • Diarrhea or

  • Virus infection or

  • Vomiting—These conditions may reduce the useful effect of the vaccine.

  • Fever or

  • Illness (moderate or severe) or

  • Weakness (severe)—The symptoms of these conditions may be confused with possible side effects of the vaccine.

  • Immune deficiency condition, family history of—May increase the chance of side effects with the vaccine.

Proper Use of poliovirus vaccine, inactivated

This section provides information on the proper use of a number of products that contain poliovirus vaccine, inactivated. It may not be specific to Ipol. Please read with care.


A nurse or other trained health professional will give you or your child this vaccine in a hospital. This vaccine is given as a shot into your muscle or under your skin.


In children, a total of 4 shots of polio vaccine are given. The shots are usually given at 2 months, 4 months, 6 to 18 months, and 4 to 6 years of age. Each dose of this vaccine is usually given at least 4 weeks apart. The first dose of this vaccine may be given to infants 6 weeks of age.


This vaccine needs to be given on a fixed schedule. If you or your child miss a scheduled shot, call your doctor to make another appointment as soon as possible.


Precautions While Using Ipol


Tell your doctor that you have received this vaccine if you plan to get any live virus vaccines within 1 month after receiving this vaccine.


Ipol Side Effects


Along with its needed effects, a medicine may cause some unwanted effects. Although not all of these side effects may occur, if they do occur they may need medical attention.


Check with your doctor or nurse immediately if any of the following side effects occur:


Symptoms of allergic reaction
  • Difficulty with breathing or swallowing

  • hives

  • itching, especially of the feet or hands

  • reddening of the skin, especially around ears

  • swelling of the eyes, face, or inside of the nose

  • unusual tiredness or weakness (sudden and severe)

More common
  • Fever over 102° F (39° C)

Some side effects may occur that usually do not need medical attention. These side effects may go away during treatment as your body adjusts to the medicine. Also, your health care professional may be able to tell you about ways to prevent or reduce some of these side effects. Check with your health care professional if any of the following side effects continue or are bothersome or if you have any questions about them:


More common
  • Irritability

  • loss of appetite

  • tiredness

Less common
  • Itching or skin rash

  • redness, soreness, hard lump, tenderness, or pain at the place of injection

Other side effects not listed may also occur in some patients. If you notice any other effects, check with your healthcare professional.


Call your doctor for medical advice about side effects. You may report side effects to the FDA at 1-800-FDA-1088.

See also: Ipol side effects (in more detail)



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More Ipol resources


  • Ipol Side Effects (in more detail)
  • Ipol Use in Pregnancy & Breastfeeding
  • Ipol Drug Interactions
  • Ipol Support Group
  • 0 Reviews for Ipol - Add your own review/rating


  • Ipol Concise Consumer Information (Cerner Multum)

  • Ipol MedFacts Consumer Leaflet (Wolters Kluwer)

  • IPOL Prescribing Information (FDA)

  • Poliovirus Vaccine Inactivated Monograph (AHFS DI)



Compare Ipol with other medications


  • Poliomyelitis Prophylaxis