Pharma company: quad pharmaceuticals
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List of quad pharmaceuticals products:
- Acetazolamide - DESCRIPTION Acetazolamide, an inhibitor of the enzyme carbonic anhydrase, is a white to faintly yellowish white crystalline, odorless powder, weakly acidic, very slightly soluble in water and slightly soluble in alcohol. The chemical name for acetazolamide is N -(5-Sulfamoyl-1,3,4-thiadiazol-2yl)-acetamide and has the following structural formula: Acetazolamide is available for...
- Acetylcysteine - 1 INDICATIONS AND USAGE CETYLEV is indicated to prevent or lessen hepatic injury after ingestion of a potentially hepatotoxic quantity of acetaminophen in patients with acute ingestion or from repeated supratherapeutic ingestion (RSI). CETYLEV is an antidote for acetaminophen overdose indicated to prevent or lessen hepatic injury after ingestion of a potentially hepatotoxic quantity of...
- Alkaban
- Aminocaproic Acid - SPL UNCLASSIFIED SECTION Rx Only DESCRIPTION Aminocaproic Acid is 6-aminohexanoic acid, which acts as an inhibitor of fibrinolysis. The structural formula is: NH 2 CH 2 (CH 2 ) 3 CH 2 COOH The molecular formula is: C 6 H 13 NO 2 Molecular Weight: 131.17 ...
- Aminohippurate Sodium
- Azathioprine - SPL UNCLASSIFIED SECTION PRODUCT INFORMATION Rx only WARNING - MALIGNANCY Chronic immunosuppression with IMURAN, a purine antimetabolite increases risk of malignancy in humans. Reports of malignancy include post-transplant lymphoma and hepatosplenic T-cell lymphoma (HSTCL) in patients with inflammatory bowel disease....
- Bacitracin - Active ingredient (each gram contains) Bacitracin 500 units Purpose First aid antibiotic Uses first aid to help prevent infection in: minor cuts scrapes burns Warnings ...
- Bethanechol - Bethanechol is a synthetic ester structurally and pharmacologically related to acetylcholine. A slowly hydrolyzed muscarinic agonist with no nicotinic effects, bethanechol is generally used to increase smooth muscle tone, as in the GI tract following abdominal surgery or in urinary retention in the absence of obstruction. It may cause hypotension, cardiac rate changes, and bronchial spasms. [PubChem] Indication: For the treatment of acute postoperative and postpartum nonobstructive (functional)...
- Bretylium - Bretylium blocks the release of noradrenaline from the peripheral sympathetic nervous system, and is used in emergency medicine, cardiology, and other specialties for the acute management of ventricular tachycardia and ventricular fibrillation. The primary mode of action for bretylium is thought to be inhibition of voltage-gated K(+) channels. Recent evidence has shown that bretylium may also inhibit the Na,K-ATPase by binding to the extracellular K-site. Indication: For use in the prophylaxis...
- Clindamycin - ZydaClin™ (clindamycin) Oral Drops liquid For Use in Dogs & Cats Equivalent to 25 mg per mL clindamycin ...
- Cytarabine - SPL UNCLASSIFIED SECTION PHARMACY BULK PACKAGE - NOT FOR DIRECT INFUSION ...
- Dacarbazine - SPL UNCLASSIFIED SECTION Rx only Hospira logo WARNING ...
- Dexamethasone - DESCRIPTION Dexamethasone tablets USP, 1.5mg for oral administration. Inactive ingredients are microcrystalline cellulose NF, anhydrous lactose NF, FD&C Red #40 aluminum lake, croscarmellose sodium NF, and magnesium stearate NF. The molecular weight for dexamethasone is 392.47. It is designated chemically as 9-fluoro-11β,17,21-trihydroxy-16α-methylpregna-1,4-diene-3,20-dione. The empirical formula is C22H29F05 and the structural formula is: ...
- Diazoxide - SPL UNCLASSIFIED SECTION FOR ORAL ADMINISTRATION Rx Only DESCRIPTION PROGLYCEM ® (diazoxide) is a nondiuretic benzothiadiazine derivative taken orally for the management of symptomatic hypoglycemia. PROGLYCEM ® Capsules contain 50 mg diazoxide, USP. The Suspension...
- Doxycycline - Pharmacological action Doxycycline is an semisynthetic tetracycline group's antibiotic of broad-spectrum. This medication has bacteriostatic action due to suppression of protein synthesis of pathogens. It active against aerobic gram-positive bacteria: Staphylococcus spp. (including strains producing penicillinase), Streptococcus spp. (including Streptococcus pneumoniae), Bacillus anthracis, Listeria monocytogenes; anaerobic bacteria: Clostridium spp. Doxycycline is also active against...
- Droperidol - SPL UNCLASSIFIED SECTION Injection, USP For Intravenous or Intramuscular Use Only Ampul R x only WARNING ...
- Erythromycin - SPL UNCLASSIFIED SECTION Film-coated Tablets Rx only To reduce the development of drug-resistant bacteria and maintain the effectiveness of Erythromycin Tablets and other antibacterial drugs, Erythromycin Tablets should be used only to treat or prevent infections that are proven or strongly suspected to be caused by bacteria. DESCRIPTION ...
- Estradiol - SPL UNCLASSIFIED SECTION ESTROGENS INCREASE THE RISK OF ENDOMETRIAL CANCER Close clinical surveillance of all women taking estrogens is important. Adequate diagnostic measures, including endometrial sampling when indicated, should be undertaken to rule out malignancy in all cases of undiagnosed persistent or recurring abnormal vaginal bleeding. There is no evidence that...
- Floxuridine - SPL UNCLASSIFIED SECTION FOR INTRA-ARTERIAL INFUSION ONLY WARNING It is recommended that Floxuridine for Injection, USP be given only by or...
- Fluorouracil - Dosage and Administration ( 2 ) 07/2016 1 INDICATIONS AND USAGE Adrucil (fluorouracil injection) is indicated for the treatment of patients with: Adrucil ® (fluorouracil injection) is a nucleoside metabolic inhibitor indicated for the treatment of...
- Glucagon - DESCRIPTION Glucagon for Injection (rDNA origin) is a polypeptidehormone identical to human glucagon that increases blood glucose and relaxessmooth muscle of the gastrointestinal tract. Glucagon is synthesized in aspecial non-pathogenic laboratory strain of Escherichiacoli bacteria that has been genetically altered by the additionof the gene for glucagon. Glucagon is a single-chainpolypeptide that contains 29 amino acid residues and has...
- Glycopyrrolate - Glycopyrrolate tablets contain the synthetic anticholinergic glycopyrrolate. Glycopyrrolate is a quaternary ammonium compound with the following chemical name: 3-[(cyclopentylhydroxyphenylacetyl)oxy]-1,1-dimethylpyrrolidinium bromide. Its empirical formula is C 19 H 28 BrNO 3 , its molecular weight is 398.33, and its structural formula is: Each 1 mg tablet contains: Glycopyrrolate, USP 1mg Each 2...
- Haloperidol - WARNING Increased Mortality in Elderly Patients with Dementia-Related Psychosis Elderly patients with dementia-related psychosis treated with antipsychotic drugs are at an increased risk of death. Analyses of seventeen placebo-controlled trials (modal duration of 10 weeks), largely in patients taking atypical antipsychotic drugs, revealed a risk of death in drug-treated patients of between 1.6 to 1.7...
- Hydrocortisone - Active Ingredients: Hydrocortisone Acetate 0.50% Purpose Anti-itch Uses: to soothe: • skin irritations • itching • dermatitis • eczema • flea bites. Warnings For external use only on adult dogs. ...
- Hydroxyprogesterone
- Isoniazid - SPL UNCLASSIFIED SECTION Rev. 02/11 Rx Only WARNING Severe and sometimes fatal hepatitis associated with isoniazid therapy has been reported and may occur or may develop even after many months of treatment. The risk of developing hepatitis is age related. Approximate case rates by age are: less than 1 per 1,000 for persons under 20 years of age, 3 per 1...
- Kanamycin - SPL UNCLASSIFIED SECTION To reduce the development of drug-resistant bacteria and maintain the effectiveness of Kanamycin Injection, USP and other antibacterial drugs, Kanamycin Injection, USP should be used only to treat or prevent infections that are proven or strongly suspected to be caused by bacteria. BOXED WARNING Patients treated with aminoglycosides by any route should be under close...
- Ketamine - A cyclohexanone derivative used for induction of anesthesia. Its mechanism of action is not well understood, but ketamine can block NMDA receptors (receptors, N-methyl-D-aspartate) and may interact with sigma receptors. [PubChem] Indication: For use as the sole anesthetic agent for diagnostic and surgical procedures that do not require skeletal muscle relaxation. Ketamine is a rapid-acting general anesthetic producing an anesthetic state characterized by profound analgesia, normal...
- Leucovorin - The active metabolite of folic acid. Leucovorin is used principally as its calcium salt as an antidote to folic acid antagonists which block the conversion of folic acid to folinic acid. [PubChem] Indication: For the treatment of osteosarcoma (after high dose methotrexate therapy). Used to diminish the toxicity and counteract the effects of impaired methotrexate elimination and of inadvertent overdosages of folic acid antagonists, and to treat megaloblastic anemias due to folic acid deficiency....
- Lincomycin - LincoMed® 300 lincomycin injection, USP Swine Antibiotic Restricted Drug (California) - Use only as Directed. For Use in Animals Only ANADA 200-368,...
- Methotrexate - WARNING: SEVERE TOXIC REACTIONS, INCLUDING EMBRYO-FETAL TOXICITY Methotrexate can cause the following severe or fatal adverse reactions. Monitor closely and modify dose or discontinue methotrexate as appropriate. • Bone marrow suppression [see Warnings and...
- Methyldopate
- Methylprednisolone - DESCRIPTION Methylprednisolone Tablets contain methylprednisolone which is a glucocorticoid. Glucocorticoids are adrenocortical steroids, both naturally occurring and synthetic, which are readily absorbed from the gastrointestinal tract. Methylprednisolone occurs as a white to practically white, odorless, crystalline powder. It is sparingly soluble in alcohol, in dioxane, and in methanol, slightly soluble in acetone, and in chloroform, and very slightly...
- Metoclopramide - Boxed Warning 8/2017 Indications and Usage ( 1 ) 8/2017 Dosage and Administration, Dosage for Gastroesophageal Reflux ( 2.2 ) 8/2017 Dosage and Administration, Dosage for Acute and...
- Metocurine Iodide - Metocurine iodide is a benzylisoquinolinium competitive nondepolarizing neuromuscular blocking agent. It is used as an anesthesia adjunct to induce skeletal muscle relaxation and to reduce the intensity of muscle contractions in convulsive therapy Metocurine iodide has a moderate risk of inducing histamine release and has some ganglion blocking activity. Metocurine iodide can be used most advantageously if muscle twitch response to peripheral nerve stimulation is monitored to assess degree of...
- Nalbuphine - A narcotic used as a pain medication. It appears to be an agonist at kappa opioid receptors and an antagonist or partial agonist at mu opioid receptors. [PubChem] Indication: For the relief of moderate to severe pain. Nalbuphine is a synthetic opioid agonist-antagonist analgesic of the phenanthrene series. Nalbuphine's analgesic potency is essentially equivalent to that of morphine on a milligram basis. The opioid antagonist activity of nalbuphine is one-fourth as potent as nalorphine and 10...
- Naloxone - A specific opiate antagonist that has no agonist activity. It is a competitive antagonist at mu, delta, and kappa opioid receptors. [PubChem] Indication: For the complete or partial reversal of narcotic depression, including respiratory depression, induced by opioids including natural and synthetic narcotics, propoxyphene, methadone and the narcotic-antagonist analgesics: nalbuphine, pentazocine and butorphanol. Naloxone is an opiate antagonist and prevents or reverses the effects of opioids...
- Nitroglycerin - SPL UNCLASSIFIED SECTION Rx DESCRIPTION: Molecular Structure Structural Formula SPL UNCLASSIFIED SECTION Molecular Structure ...
- Pancuronium - A bis-quaternary steroid that is a competitive nicotinic antagonist. As a neuromuscular blocking agent it is more potent than curare but has less effect on the circulatory system and on histamine release. Indication: Used as a muscle relaxant during anesthesia and surgical procedures. Pancuronium is a typical non-depolarising curare-mimetic muscle relaxant. It acts as a competitive acetylcholine antagonist on neuromuscular junctions, displacing acetylcholine (hence competitive) from its...
- Pralidoxime - Pralidoxime is an antidote to organophosphate pesticides and chemicals. Organophosphates bind to the esteratic site of acetylcholinesterase, which results initially in reversible inactivation of the enzyme. If given within 24 hours,after organophosphate exposure, pralidoxime reactivates the enzyme cholinesterase by cleaving the phosphate-ester bond formed between the organophosphate and acetylcholinesterase. Indication: For the treatment of poisoning due to those pesticides and chemicals of the...
- Procainamide - A derivative of procaine with less CNS action. [PubChem] Indication: For the treatment of life-threatening ventricular arrhythmias. Procainamide is an agent indicated for production of local or regional anesthesia and in the treatment of ventricular tachycardia occurring during cardiac manipulation, such as surgery or catheterization, or which may occur during acute myocardial infarction, digitalis toxicity, or other cardiac diseases. The mode of action of the antiarrhythmic effect of...
- Prochlorperazine - SPL UNCLASSIFIED SECTION ANTIEMETIC - TRANQUILIZER WARNING SPL UNCLASSIFIED SECTION Increased Mortality in Elderly Patients with Dementia-Related Psychosis Elderly patients with dementia-related psychosis treated with antipsychotic drugs are at an increased risk of death. Analyses of seventeen placebo-controlled trials...
- Protamine
- Ritodrine - Adrenergic beta-agonist used to control premature labor. [PubChem] Indication: For the treatment and prophylaxis of premature labour Beta-2 adrenergic receptors are located at sympathetic neuroeffector junctions of many organs, including uterus. Ritodrine is beta-2 adrenergic agonist. It stimulates beta-2 adrenergic receptor, increases cAMP level and decreases intracellular calcium concentration. The decrease of calcium concentration leads to a relaxation of uterine smooth muscle and, therefore...
- Sulfamethoprim - This medication is used to treat a wide variety of bacterial infections . It is also used to treat a certain type of pneumonia (pneumocystis pneumonia) in patients with a weakened immune system. This medication is a combination of 2 antibiotics: sulfamethoxazole and trimethoprim . It works by stopping the growth of bacteria and the pneumocystis fungus.
- Trifluoperazine - A phenothiazine with actions similar to chlorpromazine. It is used as an antipsychotic and an antiemetic. [PubChem] Indication: For the treatment of anxiety disorders, depressive symptoms secondary to anxiety and agitation. Trifluoperazine is a trifluoro-methyl phenothiazine derivative intended for the management of schizophrenia and other psychotic disorders. Trifluoperazine has not been shown effective in the management of behaviorial complications in patients with mental retardation.
- Tubocurarine - A neuromuscular blocker and active ingredient in curare; plant based alkaloid of Menispermaceae. [PubChem] Indication: Used as a diagnosis agent for myasthenia gravis, and also to facilitate the intubation after induction of anesthesia in surgical procedure Tubocurarine, a naturally occurring alkaloid, is used to treat smoking withdrawl syndrom.
- Vancomycin - Antibacterial obtained from Streptomyces orientalis. It is a glycopeptide related to ristocetin that inhibits bacterial cell wall assembly and is toxic to kidneys and the inner ear. [PubChem] Indication: For the treatment of serious or severe infections caused by susceptible strains of methicillin-resistant (beta-lactam-resistant) staphylococci. Vancomycin is a branched tricyclic glycosylated nonribosomal peptide produced by the fermentation of the Actinobacteria species Amycolatopsis...
- Verapamil - A calcium channel blocker that is a class IV anti-arrhythmia agent. [PubChem] Indication: For the treatment of hypertension, angina, and cluster headache prophylaxis. Verapamil is an L-type calcium channel blocker that also has antiarrythmic activity. The R-enantiomer is more effective at reducing blood pressure compared to the S-enantiomer. However, the S-enantiomer is 20 times more potent than the R-enantiomer at prolonging the PR interval in treating arrhythmias.
- Vinblastine - Antitumor alkaloid isolated from Vinca rosea. (Merck, 11th ed.) Indication: For treatment of breast cancer, testicular cancer, lymphomas, neuroblastoma, Hodgkin's and non-Hodgkin's lymphomas, mycosis fungoides, histiocytosis, and Kaposi's sarcoma. Vinblastine is a vinca alkaloid antineoplastic agent. The vinca alkaloids are structurally similar compounds comprised of 2 multiringed units: vindoline and catharanthine. The vinca alkaloids have become clinically useful since the discovery of their...
- Vincristine - Antitumor alkaloid isolated from Vinca Rosea. (Merck, 11th ed.) Indication: For treatment of acute leukaemia, malignant lymphoma, Hodgkin's disease, acute erythraemia, acute panmyelosis Vincristine is a vinca alkaloid antineoplastic agent used as a treatment for various cancers including breast cancer, Hodgkin's disease, Kaposi's sarcoma, and testicular cancer. The vinca alkaloids are structurally similar compounds comprised of 2 multiringed units, vindoline and catharanthine. The vinca...
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The information was verified by Dr. Rachana Salvi, MD Pharmacology
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