Simvastatin-corax may be available in the countries listed below.
Ingredient matches for Simvastatin-corax
Simvastatin is reported as an ingredient of Simvastatin-corax in the following countries:
- Germany
International Drug Name Search
Simvastatin-corax may be available in the countries listed below.
Simvastatin is reported as an ingredient of Simvastatin-corax in the following countries:
International Drug Name Search
Alzytec may be available in the countries listed below.
Cetirizine dihydrochloride (a derivative of Cetirizine) is reported as an ingredient of Alzytec in the following countries:
International Drug Name Search
Dotium may be available in the countries listed below.
Domperidone maleate (a derivative of Domperidone) is reported as an ingredient of Dotium in the following countries:
International Drug Name Search
Terbinafina Combix may be available in the countries listed below.
Terbinafine hydrochloride (a derivative of Terbinafine) is reported as an ingredient of Terbinafina Combix in the following countries:
International Drug Name Search
UK matches:
Rec.INN
D06BB03,J05AB01,S01AD03
0059277-89-3
C8-H11-N5-O3
225
Antiviral agent
6H-Purin-6-one, 2-amino-1,9-dihydro-9-[(2-hydroxyethoxy)methyl]-
Omalizumab may rarely cause a severe and sometimes life-threatening allergic reaction. This may occur right after receiving a dose or hours later. It may occur after the first dose or after many doses. Your doctor will monitor you for a period of time after your receive your dose of Omalizumab. Contact your doctor or seek medical care at once if you develop anxiety; chest tightness; cough; dizziness; fainting; fast or weak heartbeat; feeling unusually warm; flushing; hives; hoarseness; itching; rash; shortness of breath; swelling of the mouth, face, lips, tongue, or throat; trouble breathing; trouble swallowing; or wheezing.
Treating moderate to severe persistent asthma in certain patients who have had a positive allergy skin test and whose symptoms are not controlled by inhaled corticosteroids.
Omalizumab is an anti-immunoglobulin E (IgE) monoclonal antibody. It works by blocking your immune system's natural response to allergens, which can lead to an acute asthma attack. This action on the immune system (specifically, IgE) helps keep your air passages open and, over time, keeps asthma under better control.
Contact your doctor or health care provider right away if this applies to you.
Some medical conditions may interact with Omalizumab. Tell your doctor or pharmacist if you have any medical conditions, especially if any of the following apply to you:
Some MEDICINES MAY INTERACT with Omalizumab. However, no specific interactions with Omalizumab are known at this time.
Ask your health care provider if Omalizumab 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.
Use Omalizumab as directed by your doctor. Check the label on the medicine for exact dosing instructions.
Ask your health care provider any questions you may have about how to use Omalizumab.
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:
Bruising, itching, pain, redness, stinging, swelling, or warmth at the injection site; headache; itching and swelling of the skin; leg, arm, or ear pain; sinus inflammation.
Severe allergic reactions (rash; hives; itching; difficulty breathing; tightness in the chest; swelling of the mouth, face, lips, tongue or throat); anxiety; calf pain, swelling, or tenderness; chest pain; confusion; cough; dizziness; fainting; fast, weak, or irregular heartbeat; feeling unusually warm; flushing; hoarseness; new or worsening breathing problems or shortness of breath; numbness or tingling; one-sided weakness; speech problems; swelling of a vein; symptoms of sinus or lung infection (congestion, cough, or fever); trouble swallowing; unusual bruising or bleeding; unusual lumps, growths, or moles; unusual swelling of the hands or feet; vision problems; wheezing.
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: Omalizumab side effects (in more detail)
Contact 1-800-222-1222 (the American Association of Poison Control Centers), your local poison control center, or emergency room immediately.
Omalizumab is usually handled and stored by a health care provider. If you are using Omalizumab at home, store Omalizumab as directed by your pharmacist or health care provider. Keep Omalizumab out of the reach of children and away from pets.
This information is a summary only. It does not contain all information about Omalizumab. 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.
Agnicin may be available in the countries listed below.
Amikacin sulfate (a derivative of Amikacin) is reported as an ingredient of Agnicin in the following countries:
International Drug Name Search
In some countries, this medicine may only be approved for veterinary use.
Alfaprostol is reported as an ingredient of Alfavet in the following countries:
International Drug Name Search
Bactelan may be available in the countries listed below.
Sulfamethoxazole is reported as an ingredient of Bactelan in the following countries:
Trimethoprim is reported as an ingredient of Bactelan in the following countries:
International Drug Name Search
Cépazine may be available in the countries listed below.
Cefuroxime axetil (a derivative of Cefuroxime) is reported as an ingredient of Cépazine in the following countries:
International Drug Name Search
Sotalol Basics may be available in the countries listed below.
Sotalol hydrochloride (a derivative of Sotalol) is reported as an ingredient of Sotalol Basics in the following countries:
International Drug Name Search
Propioform may be available in the countries listed below.
Betamethasone 17α,21-dipropionate (a derivative of Betamethasone) is reported as an ingredient of Propioform in the following countries:
International Drug Name Search
There are currently no drugs listed for "Perforated Tympanic Membrane".
Definition of Perforated Tympanic Membrane: A tear in the Tympanic membrane (eardrum).
Micromedex Care Notes:
Medical Encyclopedia:
Sandoz Co-Amoxyclav may be available in the countries listed below.
Amoxicillin is reported as an ingredient of Sandoz Co-Amoxyclav in the following countries:
Clavulanic Acid is reported as an ingredient of Sandoz Co-Amoxyclav in the following countries:
International Drug Name Search
Adonamin may be available in the countries listed below.
Carbazochrome sodium sulfonate (a derivative of Carbazochrome) is reported as an ingredient of Adonamin in the following countries:
International Drug Name Search
Laxans-ratiopharm Pico may be available in the countries listed below.
Sodium Picosulfate monohydrate (a derivative of Sodium Picosulfate) is reported as an ingredient of Laxans-ratiopharm Pico in the following countries:
International Drug Name Search
Aldinir may be available in the countries listed below.
Cefdinir is reported as an ingredient of Aldinir in the following countries:
International Drug Name Search
Herpelad may be available in the countries listed below.
Aciclovir is reported as an ingredient of Herpelad in the following countries:
International Drug Name Search
Filosfil may be available in the countries listed below.
Nelfinavir mesilate (a derivative of Nelfinavir) is reported as an ingredient of Filosfil in the following countries:
International Drug Name Search
Flea-Fence Acute may be available in the countries listed below.
In some countries, this medicine may only be approved for veterinary use.
Nitenpyram is reported as an ingredient of Flea-Fence Acute in the following countries:
International Drug Name Search
Acemetacin-CT may be available in the countries listed below.
Acemetacin is reported as an ingredient of Acemetacin-CT in the following countries:
International Drug Name Search
Proparacaine Hydrochloride (USAN) is also known as Proxymetacaine (Rec.INN)
International Drug Name Search
Glossary
| Rec.INN | Recommended International Nonproprietary Name (World Health Organization) |
| USAN | United States Adopted Name |
Prophylux may be available in the countries listed below.
Propranolol hydrochloride (a derivative of Propranolol) is reported as an ingredient of Prophylux in the following countries:
International Drug Name Search
Aci-End may be available in the countries listed below.
Magaldrate is reported as an ingredient of Aci-End in the following countries:
Simeticone is reported as an ingredient of Aci-End in the following countries:
International Drug Name Search
Acetylsalicylzuur Katwijk may be available in the countries listed below.
Acetylsalicylic Acid is reported as an ingredient of Acetylsalicylzuur Katwijk in the following countries:
International Drug Name Search
Sicovit C may be available in the countries listed below.
Ascorbic Acid is reported as an ingredient of Sicovit C in the following countries:
International Drug Name Search
In some countries, this medicine may only be approved for veterinary use.
Pyrantel tartrate (a derivative of Pyrantel) is reported as an ingredient of Swine Wormer B in the following countries:
International Drug Name Search
Piam may be available in the countries listed below.
Tetryzoline hydrochloride (a derivative of Tetryzoline) is reported as an ingredient of Piam in the following countries:
International Drug Name Search
Oseltamivir Phosphate may be available in the countries listed below.
Oseltamivir Phosphate (USAN) is known as Oseltamivir in the US.
International Drug Name Search
Glossary
| USAN | United States Adopted Name |
Cilazapril-Teva may be available in the countries listed below.
Cilazapril monohydrate (a derivative of Cilazapril) is reported as an ingredient of Cilazapril-Teva in the following countries:
International Drug Name Search
Diliter may be available in the countries listed below.
Diltiazem hydrochloride (a derivative of Diltiazem) is reported as an ingredient of Diliter in the following countries:
Duloxetine is reported as an ingredient of Diliter in the following countries:
International Drug Name Search
Biocanispot may be available in the countries listed below.
In some countries, this medicine may only be approved for veterinary use.
Imidacloprid is reported as an ingredient of Biocanispot in the following countries:
International Drug Name Search
To reduce the development of drug-resistant bacteria and maintain the effectiveness of Bacitracin and other antibacterial drugs, Bacitracin should be used only to treat or prevent infections that are proven or strongly suspected to be caused by bacteria.
For Intramuscular Use
Nephrotoxicity: Bacitracin in parenteral (intramuscular) therapy may cause renal failure due to tubular and glomerular necrosis. Its use should be restricted to infants with staphylococcal pneumonia and empyema when due to organisms shown to be susceptible to bacitracin. It should be used only where adequate laboratory facilities are available and when constant supervision of the patient is possible.
Renal function should be carefully determined prior to and daily during therapy. The recommended daily dose should not be exceeded and fluid intake and urinary output should be maintained at proper levels to avoid kidney toxicity. If renal toxicity occurs the drug should be discontinued. The concurrent use of other nephrotoxic drugs, particularly streptomycin, kanamycin, polymyxin B, polymyxin E (colistin), and neomycin should be avoided.
Sterile Bacitracin, USP is an antibiotic for intramuscular administration. Bacitracin is derived from cultures of Bacillus subtilis (Tracey). It is a white to pale buff, hygroscopic powder, odorless or having a slight odor. It is freely soluble in water; insoluble in acetone, chloroform, and ether. While soluble in alcohol, methanol, and glacial acetic acid, there is some insoluble residue. It is precipitated from its solutions and inactivated by many of the heavy metals.
The structural formula is:
The molecular formula is: C66H103N17O16S. Bacitracin is comprised of a polypeptide complex and Bacitracin A is the major component in this complex. The molecular weight of Bacitracin A is 1422.71.
Bacitracin exerts pronounced antibacterial action in vitro against a variety of gram-positive and a few gram-negative organisms. However, among systemic diseases, only staphylococcal infections qualify for consideration of bacitracin therapy. Bacitracin is assayed against a standard and its activity is expressed in units, 1 mg having a potency of not less than 50 units.
Susceptibility plate testing: If the Kirby-Bauer method of disk susceptibility is used, a 10 unit bacitracin disk should give a zone of over 13 mm when tested against a bacitracin-susceptible strain of Staphylococcus aureus. Absorption of bacitracin following intramuscular injection is rapid and complete. A dose of 200 or 300 units/kg every 6 hours gives serum levels of 0.2 to 2 mcg/mL in individuals with normal renal function. The drug is excreted slowly by glomerular filtration. It is widely distributed in all body organs and is demonstrable in ascitic and pleural fluids after intramuscular injection.
In accordance with the statements in the "Warning Box", the use of intramuscular bacitracin is limited to the treatment of infants with pneumonia and empyema caused by staphylococci shown to be susceptible to the drug.
To reduce the development of drug-resistant bacteria and maintain the effectiveness of Bacitracin and other antibacterial drugs, Bacitracin should be used only to treat or prevent infections that are proven or strongly suspected to be caused by susceptible bacteria. When culture and susceptibility information are available, they should be considered in selecting or modifying antibacterial therapy. In the absence of such data, local epidemiology and susceptibility patterns may contribute to the empiric selection of therapy.
This drug is contraindicated in those individuals with a history of previous hypersensitivity or toxic reaction to it.
See "Warning Box" for precautions in regard to kidney toxicity associated with intramuscular use of bacitracin.
Clostridium difficile associated diarrhea (CDAD) has been reported with use of nearly all antibacterial agents and may range in severity from mild diarrhea to fatal colitis. Treatment with antibacterial agents alters the normal flora of the colon leading to overgrowth of C. difficile.
C. difficile produces toxins A and B which contribute to the development of CDAD. Hypertoxin producing strains of C. difficile cause increased morbidity and mortality, as these infections can be refractory to antimicrobial therapy and may require colectomy. CDAD must be considered in all patients who present with diarrhea following antibiotic use. Careful medical history is necessary since CDAD has been reported to occur over two months after the administration of antibacterial agents.
If CDAD is suspected or confirmed, ongoing antibiotic use not directed against C. difficile may need to be discontinued. Appropriate fluid and electrolyte management, protein supplementation, antibiotic treatment of C. difficile, and surgical evaluation should be instituted as clinically indicated.
Adequate fluid intake should be maintained orally, or if necessary, by parenteral method.
As with other antibiotics, use of this drug may result in overgrowth of nonsusceptible organisms, including fungi. If superinfection occurs, appropriate therapy should be instituted.
Prescribing Bacitracin in the absence of a proven or strongly suspected bacterial infection or a prophylactic indication is unlikely to provide benefit to the patient and increases the risk of the development of drug-resistant bacteria.
There have been reports of anaphylaxis and/or allergic contact dermatitis in patients exposed to Bacitracin in non-approved indications.
Patients should be counseled that antibacterial drugs, including Bacitracin, should only be used to treat bacterial infections. They do not treat viral infections (e.g., the common cold). When Bacitracin is prescribed to treat a bacterial infection, patients should be told that although it is common to feel better early in the course of therapy, the medication should be taken exactly as directed. Skipping doses or not completing the full course of therapy may (1) decrease the effectiveness of the immediate treatment and (2) increase the likelihood that bacteria will develop resistance and will not be treatable by Bacitracin or other antibacterial drugs in the future.
Diarrhea is a common problem caused by antibiotics which usually ends when the antibiotic is discontinued. Sometimes after starting treatment with antibiotics, patients can develop watery and bloody stools (with or without stomach cramps and fever) even as late as two or more months after having taken the last dose of the antibiotic. If this occurs, patients should contact their physician as soon as possible.
Nephrotoxic reactions—Albuminuria, cylindruria, azotemia. Rising blood levels without any increase in dosage.
Other reactions—Nausea and vomiting. Pain at site of injection. Skin rashes.
TO BE ADMINISTERED INTRAMUSCULARLY ONLY
Infant dose: For infants under 2500 grams—900 units/kg/24 hours in 2 or 3 divided doses. For infants over 2500 grams—1,000 units/kg/24 hours, in 2 or 3 divided doses. Intramuscular injections of the solution should be given in the upper outer quadrant of the buttocks, alternating right and left and avoiding multiple injections in the same region because of the transient pain following injection.
Should be dissolved in sodium chloride injection containing 2 percent procaine hydrochloride. The concentration of the antibiotic in the solution should not be less than 5,000 units per mL or more than 10,000 units per mL.
Diluents containing parabens should not be used to reconstitute bacitracin; cloudy solutions and precipitate formation have occurred.
Reconstitution of the 50,000 unit vial with 9.8 mL of diluent will result in a concentration of 5,000 units per mL.
Solutions are stable for one week when stored in a refrigerator 2° to 8°C (36° to 46°F).
Sterile Bacitracin, USP is available in a vial (1's) containing 50,000 units (NDC 0009-0233-01) and as a pack of ten vials (10's) each containing 50,000 units (NDC 0009-0233-03).
Store the unreconstituted product in a refrigerator 2° to 8°C (36° to 46°F).
Rx only
LAB-0026-5.0
September 2010
NDC 0009-0233-01
One Vial
Rx only
Bacitracin for
Injection, USP
For Intramuscular Use
50,000 Units
Pfizer
Distributed by
Pharmacia & Upjohn Co
Division of Pfizer Inc, NY, NY 10017
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| Marketing Information | |||
| Marketing Category | Application Number or Monograph Citation | Marketing Start Date | Marketing End Date |
| ANDA | ANDA060733 | 07/29/1948 | |
| Labeler - Pharmacia and Upjohn Company (829076566) |
| Establishment | |||
| Name | Address | ID/FEI | Operations |
| Pharmacia and Upjohn Company | 829076566 | MANUFACTURE | |
| Establishment | |||
| Name | Address | ID/FEI | Operations |
| Xellia Pharmaceuticals AS | 561816174 | MANUFACTURE | |