Pharma company: almus
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List of almus products:
- Aciclovir - Pharmacological action Aciclovir is an antiviral agent. Thymidine kinase of virus-infected cells actively converts acyclovir through a series of sequential reactions in the mono-, di- and triphosphate of acyclovir. The latter interacts with the viral DNA polymerase, and embedded in DNA, which is synthesized for new viruses. Thus it is formed a "defective" viral DNA which leads to suppression of replication of new generations of viruses. This mediciine acyclovir is active against Herpes...
- Allopurinol - Pharmacological action Allopurinol Laboratories is a medication that violates the synthesis of uric acid. This drug is a structural analog of hypoxanthine. It inhibits the enzyme xanthine oxidase, which is involved in the conversion of hypoxanthine to xanthine and xanthine to uric acid. This is due to decrease in the concentration of uric acid and its salts in body fluids and urine, which helps dissolve existing uric acid deposits and prevents their formation in tissues and kidney....
- Amiodarone - An antianginal and antiarrhythmic drug. It increases the duration of ventricular and atrial muscle action by inhibiting Na,K-activated myocardial adenosine triphosphatase. There is a resulting decrease in heart rate and in vascular resistance. [PubChem] Indication: Intravenously, for initiation of treatment and prophylaxis of frequently recurring ventricular fibrillation and hemodynamically unstable ventricular tachycardia in patients refractory to other therapy. Orally, for the treatment of...
- Amlodipine - Amlodipine is a long-acting 1,4-dihydropyridine calcium channel blocker. It acts primarily on vascular smooth muscle cells by stabilizing voltage-gated L-type calcium channels in their inactive conformation. By inhibiting the influx of calcium in smooth muscle cells, amlodipine prevents calcium-dependent myocyte contraction and vasoconstriction. A second proposed mechanism for the drug’s vasodilatory effects involves pH-dependent inhibition of calcium influx via inhibition of smooth...
- Amoxicilline
- Amoxicilline; Acide Clavulanique Adultes
- Amoxicilline; Acide Clavulanique Enfants
- Amoxicilline; Acide Clavulanique Nourrissons
- Betahistine - Betahistine is an antivertigo drug first used for treating vertigo assosicated with MГ©niГЁre’s disease. It is also commonly used for patients with balance disorders. Indication: For the reduction of episodes of vertigo association with MГ©niГЁre's disease. Betahistine primarily acts as a histamine H1-agonist with 0.07 times the activity of histamine. Stimulating the H1-receptors in the inner ear causes a vasodilatory effect and increased permeability in the blood vessels which...
- Cefixime - RECENT MAJOR CHANGES Warnings and Precautions, Risk in Patients with Phenylketonuria ( 5.6 ) 03/2017 1 INDICATIONS AND USAGE SUPRAX (cefixime) is a cephalosporin antibacterial drug indicated in the treatment of adults and pediatric patients six months and older with the following infections: ...
- Cefpodoxime - Cefpodoxime is an oral third generation cephalosporin antibiotic. It is active against most Gram positive and Gram negative bacteria. It is commonly used to treat acute otitis media, pharyngitis, and sinusitis. Cefpodoxime proxetil is a prodrug which is absorbed and de-esterified by the intestinal mucosa to Cefpodoxime. Indication: For the treatment of patients with mild to moderate infections caused by susceptible strains of the designated microorganisms. Cefpodoxime is an oral third...
- Ceftriaxone - SPL UNCLASSIFIED SECTION Rx only To reduce the development of drug-resistant bacteria and maintain the effectiveness of Ceftriaxone for Injection, USP and other antibacterial drugs, Ceftriaxone for Injection, USP should be used only to treat or prevent infections that are proven or strongly suspected to be caused by bacteria. DESCRIPTION ...
- Ciprofloxacine
- Citalopram - Pharmacological action Citalopram is an antidepressant. The mechanism of action is associated with selective blockade of the inverse of neuronal serotonin in the synapses of neurons of the CNS. Citalopram lacks or has a very weak ability to bind to histamine, m-choline- and adrenoreceptors. Pharmacokinetics After oral administration C max of citalopram in plasma is achieved within 2-4 hours. The oral bioavailability is about 80%. Changes in plasma concentrations of citalopram are...
- Clarithromycine
- Dextropropoxyphene; Paracetamol
- Dextropropoxyphene; Paracetamol; Cafeine
- Domperidone - SPL UNCLASSIFIED SECTION CAUTION Federal law (USA) restricts this drug to use by or on the order of a licensed veterinarian. For oral use in horses only. DESCRIPTION Domperidone is D 2 dopamine receptor antagonist. Chemically, domperidone is ...
- Enalapril - Enalapril information Enalapril is one of the most effective anti-hypertensive drugs in the market. Belonging to the angiotensin-converting-enzyme inhibitors (ACE inhibitors) category of drugs, Enalapril helps to keep raising blood pressure under control thereby reducing the risk factors of this disease. Since hypertension works out the heart muscles to cause early arterial failure, Enalapril stands in the way and helps to keep your heart healthy, indirectly. Like all other ACE inhibitors,...
- Fenofibrate - 1 INDICATIONS AND USAGE Fenofibrate tablets are a peroxisome proliferator receptor alpha (PPARα) activator indicated as an adjunct to diet: To reduce elevated LDL-C, Total-C, TG and Apo B, and to increase HDL C in adult patients with primary hypercholesterolemia or...
- Finasteride - 1 INDICATIONS AND USAGE PROSCAR, is a 5α-reductase inhibitor, indicated for the treatment of symptomatic benign prostatic hyperplasia (BPH) in men with an enlarged prostate to ( 1.1 ): Improve symptoms Reduce the risk of acute urinary retention Reduce the risk of the need for surgery including transurethral resection of the prostate (TURP)...
- Fluconazole - Pharmacological action Fluconazole is an antifungal drug from the group of triazole derivatives. Inhibits the synthesis of ergosterol disrupting the permeability of the cell wall. This medication is active against Candida, Microsporum, Cryptococcus neoformans, Trichophyton. Pharmacokinetics Fluconazole is well absorbed after oral administration. Simultaneous ingestion does not affect absorption. The bioavailability is 90%. Fluconazole is widely distributed in tissues and organs of the...
- Fluoxetine - Pharmacological action Fluoxetine is an antidepressant, propylamine derivative. The mechanism of action is associated with selective blockade of the inverse of neuronal serotonin reuptake in the CNS. Fluoxetine is a weak antagonist of choline, adrenergic and histamine receptors. Unlike most antidepressants fluoxetine apparently does not cause reduction of functional activity of postsynaptic beta-adrenergic receptors. This medication improves mood, reduces anxiety and stress, eliminates...
- Gliclazide - Gliclazide is an oral antihyperglycemic agent used for the treatment of non-insulin-dependent diabetes mellitus (NIDDM). It belongs to the sulfonylurea class of insulin secretagogues, which act by stimulating β cells of the pancreas to release insulin. Sulfonylureas increase both basal insulin secretion and meal-stimulated insulin release. Medications in this class differ in their dose, rate of absorption, duration of action, route of elimination and binding site on their target pancreatic...
- Ibuprofene - Pharmacological action NSAIDs, a derivative of phenylpropionic acid, ibuprofen has anti-inflammatory, analgesic and antipyretic effect. The mechanism of action is associated with inhibition of COX activity - the main enzyme metabolism of arachidonic acid, which is a precursor of prostaglandins, which play a major role in the pathogenesis of inflammation, pain and fever. Analgesic effect is due to both peripheral (indirectly, through suppression of prostaglandin synthesis), and a central...
- Lactulose - DESCRIPTION Lactulose is a synthetic disaccharide in solution form for oral administration. Each 15 mL of Lactulose Solution contains: 10 g lactulose (and less than 1.6 g galactose, less than 1.2 g lactose, and 1.2 g or less of other sugars). Also contains FD&C Yellow No. 6, purified water, and flavoring. Sodium hydroxide used to adjust pH . The pH range is 2.5 to 6.5. Lactulose is a colonic acidifier which promotes laxation. The...
- Lamotrigine - WARNING: SERIOUS SKIN RASHES See full prescribing information for complete boxed warning. Cases of life-threatening serious rashes, including Stevens-Johnson syndrome and toxic...
- Lamprene
- Lansoprazole - Active ingredient (in each capsule) Lansoprazole 15 mg Purpose Acid reducer Use • treats frequent heartburn (occurs 2 or more days a week) • not intended for immediate relief of heartburn; this drug may take 1 to 4 days for full...
- Lisinopril - WARNING: FETAL TOXICITY • When pregnancy is detected, discontinue lisinopril as soon as possible [see Warnings and Precautions (5.1) ]. • Drugs that act directly on the renin-angiotensin system can cause injury and death to the developing fetus [see ...
- Loratadine - Active ingredient (in each tablet) Loratadine 10 mg Purpose Antihistamine Uses temporarily relieves these symptoms due to hay fever or other upper respiratory allergies: • runny nose • itchy, watery eyes ...
- Mianserine
- Ofloxacine - Pharmacological action Ofloxacin is an antimicrobial agents of broad-spectrum action type from fluoroquinolone group. Bactericidal action of ofloxacin is due to blockage of the enzyme DNA gyrase in bacterial cells. This medication is highly active against most of gram-negative bacteria: Escherichia coli, Salmonella spp., Shigella spp., Proteus spp., Morganella morganii, Klebsiella spp. (including Klebsiella pneumoniae), Enterobacter spp., Serratia spp., Citrobacter spp., Yersinia spp.,...
- Omeprazole - WARNINGS AND PRECAUTIONS Bone Fracture ( 5.3 ) 09/2010 WARNINGS AND PRECAUTIONS Diminished anti-platelet activity of clopidogrel ( 5.4 ) 01/2011 ...
- Pantoprazole - Pantoprazole is a proton pump inhibitor drug used for short-term treatment of erosion and ulceration of the esophagus caused by gastroesophageal reflux disease. Indication: Short-term (up to 16 weeks) treatment of erosive esophagitis. Pantoprazole is a substituted benzimidazole indicated for the short-term treatment (up to 16 weeks) in the healing and symptomatic relief of erosive esophagitis. Pantoprazole is a proton pump inhibitor (PPI) that suppresses the final step in gastric acid...
- Paracetamol - Pharmacological action Paracetamol is an analgesic-antipyretic. It has analgesic, antipyretic and weak anti-inflammatory action. The mechanism of action is associated with inhibition of prostaglandin synthesis, the predominant influence on the thermoregulation center in the hypothalamus, enhances heat transfer. Why is Paracetamol prescribed? Pain weak and moderate intensity of different genesis (including headache, migraine, toothache, neuralgia, myalgia, algomenorrhea; pain in trauma,...
- Paracetamol; Codeine
- Pravastatine
- Prednisone - SPL UNCLASSIFIED SECTION Rx only DESCRIPTION Prednisone Tablets USP are available for oral administration containing either 1 mg, 2.5 mg, 5 mg, 10 mg, 20 mg or 50 mg of prednisone USP. Each tablet contains the following inactive ingredients: lactose monohydrate, magnesium stearate, microcrystalline cellulose, pregelatinized starch, sodium starch glycolate and stearic acid (1 mg, 2.5 mg, and 5 mg only). ...
- Ramipril - Ramipril information Ramipril belongs to the class of drugs classified as ACE inhibitors or Angiotensin-Converting-Enzyme inhibitor. Ramipril indications This product is a drug prescribed for the treatment of hypertension or high blood pressure, and for the prevention of heart failures succeeding heart attacks. Ramipril is also used for the prevention of heart attacks, stroke and other heart related problems. Ramipril warnings The medication is major allergen especially to patients...
- Risperidone - Risperidone information This medication works well for patients suffering from the agonies of bipolar diseases. Mostly, Risperidone helps individuals with schizophrenia and mania. By affecting the functions of different chemicals in the brain, this drug may provide relief to sufferers. However, before using this drug, patients need to be sure about the side effects that may occur. Risperidone can also be used for treating other disorders or as a complementary drug. Risperidone warnings ...
- Roxithromycine
- Sertraline - Pharmacological action Sertraline (with the generic name of Sertraline) belongs to the groups of drugs known as selective serotonin reuptake inhibitors. These selective serotonin reuptake drugs influence chemical imbalance in the brain responsible for depression, panic anxiety, obsessive compulsive disorder and others. Why is Sertraline prescribed? Sertraline is indicated for the treatment of: depression panic anxiety disorders obsessive compulsive disorder PSTD or post traumatic...
- Simvastatine - Pharmacological action Simvastatin is a hypolipidemic agent from a group of statins, an inhibitor of HMG-CoA reductase. This medication is a prodrug because it has in its structure the closed lactone ring which is hydrolyzed after intake. Lipid-lowering effect of statins is associated with lower levels of total cholesterol by LDL-C. Reducing cholesterol is dose-dependent and is not linear but exponential. Statins do not affect the activity of lipoprotein and hepatic lipase, have no...
- Sotalol - An adrenergic beta-antagonist that is used in the treatment of life-threatening arrhythmias. [PubChem] Indication: For the maintenance of normal sinus rhythm [delay in time to recurrence of atrial fibrillation/atrial flutter (AFIB/AFL)] in patients with symptomatic AFIB/AFL who are currently in sinus rhythm. Also for the treatment of documented life-threatening ventricular arrhythmias. Sotalol is an antiarrhythmic drug. It falls into the class of beta blockers (and class II antiarrhythmic...
- Tamsulosine LP
- Terbinafine - Terbinafine information Terbinafine is an antifungal drug used as athlete's foot medication. Terbinafine works like an antibiotic to treat fungal infections. Terbinafine indications This medicine is mainly indicated to treat fungal infections of the fingernails and toenails. Terbinafine may also be used for purposes not mentioned here. Terbinafine warnings This drug is classed as a FDA pregnancy category B drug and may cause severe side effects to an unborn baby. Consult with your...
- Trimebutine - Trimebutine belongs to the class of medications called spasmolytics . It is used to treat irritable bowel syndrome (spastic colon). This condition is caused by overactive movements of the bowels. Trimebutine works by slowing down or normalizing the abnormal movements of the bowel. Your doctor may have suggested this medication for conditions other than those listed in these drug information articles. As well, some forms of this medication may not be used for all of the conditions...
- Venlafaxine LP
- Zolpidem - Zolpidem is a prescription short-acting nonbenzodiazepine hypnotic that potentiates gamma-aminobutyric acid (GABA), an inhibitory neurotransmitter, by binding to benzodiazepine receptors which are located on the gamma-aminobutyric acid receptors. Zolpidem is used for the short-term treatment of insomnia. It works quickly (usually within 15 minutes) and has a short half-life (2-3 hours). It is classified as an imidazopyridine. As an anticonvulsant and muscle relaxant, the beneficial effects...
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The information was verified by Dr. Rachana Salvi, MD Pharmacology
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