Pharma company: siam pharmaceutical
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List of siam pharmaceutical products:
- A-Mol - Pharmacological action Acetaminophen 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 Acetaminophen prescribed? Pain weak and moderate intensity of different genesis (including headache, migraine, toothache, neuralgia, myalgia, algomenorrhea; pain in...
- A-Mol Pediatric - Pharmacological action Acetaminophen 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 Acetaminophen prescribed? Pain weak and moderate intensity of different genesis (including headache, migraine, toothache, neuralgia, myalgia, algomenorrhea; pain in...
- A-Mol Plus
- Almaxane Suspension
- Almaxane Tablets
- Ampicyn - Pharmacological action Ampicillin is an antibiotic of semisynthetic broad-spectrum penicillin group. This medication has a bactericidal effect by suppressing the synthesis of bacterial cell walls. Ampicillin is active against aerobic gram-positive bacteria: Staphylococcus spp. (with the exception of strains producing penicillinase), Streptococcus spp., Enterococcus spp., Listeria monocytogenes; aerobic gram-negative bacteria: Neisseria gonorrhoeae, Neisseria meningitidis, Escherichia coli,...
- Annoxen
- Annoxen-S
- Antazallerge
- Astahis
- Bromesep
- Bromesep Expectorant
- Bronchil
- Buprine
- CEF-3
- Cal-Os
- Calmaril
- Cavumox
- Cefxitin
- Chloracil
- Cibis
- Cifloxin
- Cipasid
- Claraxim
- Claron
- Cloxalin
- Defungo - Pharmacological action Clotrimazole is an antifungal agent of imidazole derivatives group for topical use. This medication has an effect at the expense of the synthesis of ergosterol, which is part of the cell membrane of fungi. Clotrimazole has a broad spectrum of action. Clotrimazole is active against dermatophytes, molds, fungi of the genus Candida, Malassezia furfur. This drug is also active against Corynebacterium minutissimum, Streptococcus spp., Staphylococcus spp., Trichomonas...
- Denson
- Deproxin
- Detuss Syrup
- Detuss Tablets - Pharmacological action Dextromethorphan is an antitussive medication. Inhibiting the excitability of the cough center this medicine suppresses the cough of any origin. Dextromethorphan has not addiction effects and it has no analgesic and hypnotic action. Dextromethorphan starts to act after 10-30 minutes after oral administration, the duration of therapeutic action: 5-6 hours for adults and 6-9 hours for children. Dextromethorphan is an optical isomer of levomethorphan which is similar to...
- Diaclaron
- Diasgest
- Dilomil
- Dipazide
- Disol
- Ditizem
- Ditrenil
- Dixocillin
- Dosanac
- Endogest
- Erimycin
- Eyedex
- Fazolin
- Fenamic
- Flamic - Pharmacological action Piroxicam is a NSAID, refers to a group oxicams. This medication has anti-inflammatory, analgesic and antipyretic effect. The mechanism of action associated with inhibition of the enzyme COX, which leads to inhibition of prostaglandin synthesis from arachidonic acid. Piroxicam inhibits the aggregation of platelets. For systemic use this medicine reduces the pain syndrome. When Piroxicam used externally it weakens or suppresses inflammation and joint pain at rest...
- Flucozole - 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...
- Folivit
- Furetic - Pharmacological action Furosemide is a loop diuretic. This medication violates the reabsorption of sodium and chlorine in the large segment of the ascending loop of Henle. Due to increasing separation of sodium ions occurs secondary (indirect osmotically bound water) increased excretion of water and increased secretion of potassium ions in the distal renal tubule. Simultaneously increased excretion of calcium and magnesium ions. Furosemide has secondary effects caused by the release of...
- Furoxime
- Gemfibril - Gemfibrozil information Gemfibrozil is a drug which is usually prescribed along with a diet to people who have very high levels of serum triglycerides (triglycerides are fatty substances from the blood) and who are at a risk of developing pancreatitis (this is the inflammation of the pancreas). This medication may also be used in order to reduce the risk of developing coronary heart disease in people who have not responded to the other therapy options: weight loss, exercises, and diet and...
- Glycemin
- Glyceol
- Glycon - Metformin belongs to the class of medications called oral hypoglycemics, which are medications that lower blood sugar. It is used to control blood glucose (blood sugar) for people with type 2 diabetes. It is used when diet, exercise, and weight reduction have not been found to lower blood glucose well enough on their own. Metformin works by reducing the amount of glucose made by the liver and by making it easier for glucose to enter into the tissues of the body. Metformin has been found...
- Grammicin
- Grammixin
- Hartsorb
- Heidi - 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...
- Histan
- Ibiamox
- Ibilex
- Ibimicyn
- Ibufen - 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...
- Inopin
- Isopen
- Kaprofen - Pharmacological action Ketoprofen is a NSAID, propionic acid derivative. This medication has analgesic, anti-inflammatory and antipyretic activity. The mechanism of action is associated with inhibition of COX activity - the main enzyme metabolism of arachidonic acid, a precursor of prostaglandins, which play a major role in the pathogenesis of inflammation, pain and fever. A pronounced analgesic effect of ketoprofen is due to two mechanisms: peripheral (indirect, via inhibition of...
- Ketazon
- Keten
- Kinline
- Lingo
- Lispril - Lisinopril information Lisinopril is a popular drug that belongs to a wide class of medicines generally known as ACE inhibitors (angiotensin converting enzyme inhibitors). This product is generally prescribed to patients who are suffering from congestive heart failure, high blood pressure or to patients who have recently suffered a heart attack. Lisinopril indications This medication is a well known medicine that is generally prescribed to patients who are suffering from heart medical...
- Lispril Hydrochlorothiazide
- Lochol - 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...
- Lomide
- Lopress
- Lorapam - Pharmacological action Lorazepam is an anxiolytic drug (tranquilizer), a derivative of benzodiazepine. This medication has anxiolytic, sedative, hypnotic, anticonvulsant, muscle relaxant central, antiemetic effect. The mechanism of the anxiolytic, sedative and hypnotic action is associated with increased inhibitory effect of GABA in the CNS. Anticonvulsant action, apparently in part due to increased presynaptic inhibition; inhibited the spread of epileptogenic activity arising in the...
- Lorsedin
- Mapezine
- Metrim
- Metrolex - Pharmacological action Metronidazole is an anti protozoal agent. It is believed that the mechanism of action is associated with DNA damage-sensitive microorganisms. Active against Trichomonas vaginalis, Gardnerella vaginalis, Giardia lamblia, Entamoeba histolytica, and obligate anaerobic bacteria (including Bacteroides spp., Fusobacterium spp.). Aerobic bacteria are resistant to metronidazole. In combination with amoxicillin Metronidazole is active against Helicobacter pylori. It is...
- Molax
- Myoflex - Trolamine salicylate is used to treat minor aches and pains of the muscles/joints (such as arthritis , backache, sprains). It belongs to a class of drugs known as salicylates.
- Myolax
- Nalopril
- Nausil
- Norxacin
- O-Sid
- Ofloxcin - 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.,...
- Painza
- Paranal - Pharmacological action Acetaminophen 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 Acetaminophen prescribed? Pain weak and moderate intensity of different genesis (including headache, migraine, toothache, neuralgia, myalgia, algomenorrhea; pain in...
- Paranal-L - Pharmacological action Acetaminophen 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 Acetaminophen prescribed? Pain weak and moderate intensity of different genesis (including headache, migraine, toothache, neuralgia, myalgia, algomenorrhea; pain in...
- Pepfamin
- Polyclox
- Prophedin
- Rifam
- Rifamiso
- Rosil
- Rothricin
- Setin
- Sia-Mox
- Siadocin
- Sialexin
- Siamdopa
- Siamformet
- Siamidine
- Siamik
- Siampicil
- Siampraxol - Pharmacological action Alprazolam is an anxiolytic drug (tranquilizer), a derivative of triazolo-benzodiazepine. This medication has anxiolytic, sedative, hypnotic, anticonvulsant, central muscle relaxant effect. The mechanism of action is to enhance the inhibitory effect of endogenous GABA in the CNS by increasing the sensitivity of the GABA-receptor mediator as a result of stimulation of benzodiazepine receptors located in the allosteric center of postsynaptic GABA-receptor activating...
- Siarizine
- Siclot
- Sifaclor
- Simacort
- Simoph Tears
- Simoyiam
- Sipam
- Sipental
- Spazol
- Sugril
- Sulam
- Sulcef
- Supralan
- Supralan-N
- Sycold
- T-ZA
- Tauglicolo
- Tenax
- Tenolol - Pharmacological action Atenolol is a cardioselective beta1-blocker without intrinsic sympathomimetic activity. This medication has antihypertensive, antianginal and antiarrhythmic action. Atenolol reduces the stimulatory effect on the heart sympathetic innervation and circulating catecholamines. The hypotensive effect of this drug is associated with a decrease in minute volume of blood, decreased activity of the renin-angiotensin system (has a greater significance for patients with...
- Terfen
- Tranclor
- Ulcefate
- Ulsanic
- Vilerm
- Zantidon - Pharmacological action Ranitidine is a blocker of histamine H2-receptors. Inhibits basal and stimulated by histamine, gastrin and acetylcholine (to a lesser extent) the secretion of hydrochloric acid. Increases the pH of gastric contents and reduces the activity of pepsin. The duration of action of ranitidine with a single admission - 12 hours. Pharmacokinetics After oral administration, ranitidine is rapidly absorbed from the gastrointestinal tract. Eating and antacids significantly...
- Zeben
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The information was verified by Dr. Rachana Salvi, MD Pharmacology
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