92 Products

- LEVOCETIRIZINE 5mg Uses Levocetirizine is an antihistamine used to relieve allergy symptoms such as watery eyes

- runny nose

- itching eyes/nose

- sneezing

- LEVOCETIRIZINE 2.5mg

- AMBROXOL 60mg

- PHENYLEPHRINE 5mg

- Paracetamol 325mg

- PARACETAMOL 325mg

- PHENYLEPHRINE 5 mg Hydrochloride

- CAFFEINE 30mg

- DIPHENHYDRAMINE 25mg

- PARACETAMOL 325mg

- CHLORPHENIRAMINE MALEATE 2mg

- PHENYLEPHRINE HYDROCHLORIDE 5mg

- CAFFEINE16mg

- DIACERIN 50mg

- GLUCOSAMINE 750mg

- MSM 200mg

- MULTIVITAMIN

- BAREC (RABEPRAZOLE 20 MG) is used to treat certain stomach and esophagus problems (such as acid reflux

- ulcers). It works by decreasing the amount of acid your stomach makes. It relieves symptoms such as heartburn

- difficulty swallowing

- and persistent cough PHARMACOLOGY PHARMACODYNAMICS: Mechanism of Action: – Rabeprazole sodium belongs to the class of anti-secretory compounds

- TRYPSIN 48mg

- BROMELAIN 90mg

- RUSTOSIDE 100mg

- DICLOFENAC 50mg   PHARMACOLOGY A.) PHARMACODYNAMICS: On being absorbed

- Fluconazole is used to treat vaginal yeast infections. It works by stopping the growth of common types of vaginal yeast (fungus). This medication belongs to a class of drugs called azole antifungals. How to use Fluconazole Tablet Azole Antifungals-Systemic Read the Patient Information Leaflet before you start taking fluconazole and each time you get a refill. If you have any questions

- ask your doctor or pharmacist. In Canada

- some brands of this medication are available without a prescription. Before taking over-the-counter fluconazole

- read the product instructions and talk to your doctor if this is your first vaginal yeast infection

- A drug that has been used in various urinary syndromes and as an antispasmodic. It may have local anesthetic activity and direct relaxing effects on smooth muscle as well as some activity as a muscarinic antagonist.   Pharmacodynamics: - Flavoxate is a spasmolytic flavone derivative that acts by relaxing the smooth muscle in the urinary tract. Flavoxate is a competitive muscarinic receptor antagonist indicated for the treatment of overactive bladder with symptoms of urge urinary incontinence

- urgency

- and urinary frequency. Muscarinic receptors play an important role in several major cholin-ergically mediated functions

- including contractions of urinary bladder smooth muscle and stimulation of salivary secretion. Mechanism of action Flavoxate acts as a direct antagonist at muscarinic acetylcholine receptors in cholinergically innervated organs. Its anticholinergic-parasympatholytic action reduces the tonus of smooth muscle in the bladder

- CALCIUM CITRATE 1000mg

- MAGNESIUM HYDROCHLORIDE 100mg

- ZINC 4mg

- VITAMIN D3 200 I.U This combination medication is used to prevent or treat low blood calcium levels in people who do not get enough calcium from their diets. It may be used to treat conditions caused by low calcium levels such as bone loss (osteoporosis)

- ETORICOXIB 60mg

- THIOCOLCHICOSIDE 4mg

- ONDANSETRON 4mg

- MOUTH DISSOLVING TABLETS

- LEVOFLOXACIN 500mg PHARMACODYNAMICS: - Levofloxacin

- a fluoroquinolone antiinfective

- is the optically active L-isomer of ofloxacin. Levofloxacin is used to treat bacterial conjunctivitis

- sinusitis

- FEXOFENADINE120mg

- MONTELUKAST10mg   Metabolism May Be Increased With Rifampicin

- Phenobarbital

- Phenytoin. Peripheral Oedema May Occur With Prednisone.   Mechanism of Action of Montelukast 10mg + Fexofenadine 120mg: Montelukast Is A Selective Leukotriene Receptor Antagonist That Blocks The Effects Of Cysteinyl Leukotrienes In The Airways. Absorption: Rapidly Absorbed From The GI Tract (Oral). Peak Plasma Concentrations In 2-4 Hr. Mean Oral Bioavailability: 64%. Distribution: Protein-Binding: >99%. Metabolism: Extensively Hepatic By CYP3A4

- Cefixime

- an antibiotic

- is a third-generation cephalosporin like ceftriaxone and cefotaxime. Cefixime is highly stable in the presence of beta-lactamase enzymes. As a result

- many organisms resistant to penicillins and some cephalosporins due to the presence of beta-lactamases

- Cefixime

- an antibiotic

- is a third-generation cephalosporin like ceftriaxone and cefotaxime. Cefixime is highly stable in the presence of beta-lactamase enzymes. As a result

- many organisms resistant to penicillins and some cephalosporins due to the presence of beta-lactamases

- BRAND NAME: - FYCEF-AZ LB COMPOSITION: - CEFIXIME 200 mg + AZITHROMYCIN 250 mg + LACTIC ACID BACILLUS 60 MILLION SPORES PACKING: - 10X1X10 (ALU-ALU) M.R.P: - 2200/- A new combination of CEFIXIME AND AZITHROMYCIN is used for the treatment of upper and lower respiratory tract infection. Cefixime

- an antibiotic

- is a third-generation cephalosporin like ceftriaxone and cefotaxime. Cefixime is highly stable in the presence of beta-lactamase enzymes. As a result

- many organisms resistant to penicillins and some cephalosporins due to the presence of beta-lactamases

- CEFIXIME 200mg

- CLAVUNIC ACID 125mg Cefixime

- an antibiotic

- is a third-generation cephalosporin like ceftriaxone and cefotaxime. Cefixime is highly stable in the presence of beta-lactamase enzymes. As a result

- CEFIXIME 200mg

- LACTIC ACID BACILLUS 2.5BILLION Cefixime

- an antibiotic

- is a third-generation cephalosporin like ceftriaxone and cefotaxime. Cefixime is highly stable in the presence of beta-lactamase enzymes. As a result

- BRAND NAME: - FYCEF-O LB COMPOSITION: - CEFIXIME 200 mg

- OFLOXACIN 200 mg

- LACTIC ACID BACILLUS 60 MILLION SPORES PACKING: - 10X1X10 (ALU-ALU) M.R.P: - 1790/- CEFIXIME 200 mg:  - Cefixime is an antibiotic. It kills the bacteria by attacking their cell wall. Specifically

- it prevents the synthesis of a substance in the cell wall called peptidoglycan

- CEFIXIME 200mg

- OFLOXACIN 200mg Cefixime is an orally active 3rd generation cephalosporin which exerts its bactericidal action against both gram positive & gram negative organisms by inhibiting bacterial cell wall synthesis. Cefixime inhibits transpeptidase & thus prevents cross linking of bacterial cell wall. Transpeptidase & associated proteins constitute various types of specific binding proteins which have affinity for cephalosporins like Cefixime. It is highly active against enterobacteriaceae

- Haemophilus influenzae

- Streptococcus pyogens & Streptococcus pneumonia &many beta lactamase producing bacteria. Ofloxacin is a bactericidal drug. It act by inhibiting the enzyme DNA gyrase (Topoisomerase 2) and Topoisomerase 4.DNA gyrase helps in the formation of a highly condensed three dimensional structure of the DNA by its nicking and closing activity and also by introducing negative supercoil in to the DNA double helix. Ofloxacin inhibits DNA gyrase which results in abnormal linkage between opened DNA and gyrase and negative supercoiling is also impaired. This will inhibits transcription of DNA in to RNA and subsequent protein synthesis. Lactic Acid Bacillus - Protects & restores the intestinal microflora - Prevents diarrhoea & dyspepsia - Maintains the intestinal pH & inhibits the growth of pathogens

- COMPOSITION: -LINEZOLID 600 MG Packing: - 10X1X4 M.R.P: - 2400   PHARMACOLOGY PHARMACOKINETICS: Absorption: Owing to hepatic first-pass metabolism

- its bioavailability is only about 60%. Distribution: Plasma protein binding of ondansetron as measured in vitro was 70% to 76%

- over the pharmacologic concentration range of 10 to 500 ng/mL. Circulating drug also distributes into erythrocytes. Metabolism: Ondansetron is extensively metabolized in humans

- with approximately 5% of a radiolabeled dose recovered as the parent compound from the urine. The primary metabolic pathway is hydroxylation on the indole ring followed by subsequent glucuronide or sulfate conjugation. Elimination: In adult cancer patients

- MEBEVERINE HYDROCHLORIDE 135mg

- CHLORDIAZEPOXIDE 5mg Packing: -10X10 M.R.P: - 1100   Mebeverine HCl is a musculotropic antispasmodic drug without atropic side-effects whose major therapeutic role is in the treatment of irritable bowel syndrome. It is also indicated for treatment of gastrointestinal spasm secondary to organic disorder. Chlordiazepoxide is a sedative/hypnotic drug and benzodiazepine derivative. Chlordiazepoxide has a medium to long half life but its active metabolite has a very long half life. The drug has amnestic

- anxiolytic

- hypnotic and skeletal muscle relaxant properties. PHARMACOKINETICS MEBEVERINE ABSORPTION: – Rapidly absorbed from the GI tract (oral); peak plasma concentrations within 1-3 hr. DISTRIBUTION: – Protein-binding: 75% to albumin. METABOLISM: – Hydrolysed completely in the liver to veratric acid and mebeverine alcohol. EXCRETION: – Via urine (as metabolites).   CHLORDIAZEPOXIDE ABSORPTION: – Rapidly absorbed following oral administration. PROTEIN BINDING: – Approximately 40% bound to plasma proteins. METABOLISM: – Chlorothiazide is not metabolized but is eliminated rapidly by the kidney. EXCRETION: – Chlorothiazide is not metabolized but is eliminated rapidly by the kidney. After oral doses

- DICLOFENAC POTASSIUM 50mg

- SERRATIOPEPTIDASE 10mg

- MECOBALAMIN 500 MG

- GABAPENTIN 300 MG Packing: - 10x10 M.R.P: -1050   Methylcobalamin and Gabapentin combination is useful for the treatment of neuropathic disorders or seizure disorders. Gabapentin can also be used to treat partial seizures in children between the ages of three and 12. Methylcobalamin is a form of vitamin B that is used to prevent postherpetic neuralgia

- neuralgia intercostals

- and diabetic neuropathy. Gabapentin is an anti-convulsant that prevents repeated electrical signals in the brain that cause seizures and is used to treat epilepsy or other similar disorders.

- MECOBALAMIN 1500mcg

- ALPHA LIPOIC ACID 300mg

- VITAMIN B2 10mg

- B6 3mg

- ACEBROPHYLLINE 200 MG Packing: -10X10 M.R.P: - 1420   ACEBROPHYLLINE HAS 3 ACTIONS NAMELY BRONCHODILATION

- MUCOREGULATION & ANTI-INFLAMMATORY ACTION. PHARMACOLOGY A.) PHARMACODYNAMICS: Acebrophylline inhibits intracellular phosphodiesterase associated significantly reduce the airway inflammation and obstruction in chronic stages. Acebrophylline increases the synthesis and release of alveolar surfactant

- resulting in triple action: mucoregulation

- stimulation of bronchoalveolar clearance

- PANTOPRAZOLE 40 MG Packing: - 10X10 M.R.P: -550   PANTOPRAZOLE 40 MG is a proton pump inhibitor drug used for short-term treatment of erosion and ulceration of the esophagus caused by gastroesophageal reflux disease. It can be used as a maintenance therapy for long term use after initial response is obtained. Pharmacokinetics Pantoprazole inhibits H+/K+ ATPase pump function thereby reducing gastric acid secretion. It also has a role in the eradication of H. pylori. Absorption : -Well absorbed; peak plasma concentrations: Approx 2-2.5 hr after oral dose. Oral bioavailability: Approx 77% with enteric-coated formulation (does not vary after single or multiple doses). Distribution Protein-binding: 98%; volume of distribution: 11-24 L. Metabolism Hepatic; mainly by cytochrome CYP2C19 and slightly by CYP2D6 and CYP2C0. Excretion Via urine (approx 80%) and bile (approx 20%). Elimination half life: approx 1 hour (prolonged in hepatic impairment; in patients with cirrhosis the elimination half life may be 3-10 hours).

- PANTOPRAZOLE 40 MG

- DOMPERIDONE 10 MG Packing: -10X10 M.R.P: - 650   PANTOPRAZOLE 40 MG & DOMPERIDONE 10 MG: - Pantoprazole is a proton pump inhibitor drug used for short-term treatment of erosion and ulceration of the esophagus caused by gastroesophageal reflux disease whereas Domperidone is a specific blocker of dopamine receptors. It speeds gastrointestinal peristalsis

- causes prolactin release

- and is used as antiemetic. Pantoprazole acts by selectively inhibiting the H+/K+-ATPase enzyme in the secretory canaliculus of the stimulated parietal cell. Domperidone stimulates GI activity by acting as a competitive antagonist at dopamine D2-receptors. Pharmacology: Pantoprazole: Pantoprazole is a proton pump inhibitor (PPI) that suppresses the final step in gastric acid production. Pantoprazole is unstable in acid and is administered orally in the form of an enteric-coated tablet Pantoprazole is completely and rapidly absorbed after oral administration. The absolute bioavailability from the tablet was found to be about 77 %. Pantoprazole is extensively metabolized in the liver through the cytochrome P450 (CYP) system. Renal elimination represents the major route of excretion (about 80%) for the metabolites of Pantoprazole; the rest is excreted with the faeces. Domperidone: Domperidone acts as a gastrointestinal emptying (delayed) adjunct and peristaltic stimulant. The gastroprokinetic properties of Domperidone are related to its peripheral dopamine receptor blocking properties.. In fasting subjects

- CEFPODOXIME 200 MG Packing: - 10X10 M.R.P: -2490   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. PHARMACODYNAMICS: - Cefpodoxime is an oral third generation cephalosporin antibiotic. It is active against most Gram positive and Gram negative bacteria. Notable exceptions include Pseudomonas aeruginosa

- Enterococcus

- CEFPODOXIME 200 MG

- CLAVUNANIC ACID 125 MG Packing: - 1X10 M.R.P: -270   Cefpodoxime and Clavulanic acid combination are effective against multiple infections. The pharmacological action of Clavulanic acid prevents hydrolysis of Cefpodoxime against beta-lactamase secreting microbes and increases the antibiotic spectrum. Cefpodoxime

- an antibiotic belongs to class of third-generation cephalosporins

- is indicated for the treatment of systemic infections including respiratory tract infections

- OFLOXACIN 200 MG Packing: - 10X10 M.R.P: - 650   Pharmacodynamics Ofloxacin is a quinolone/fluoroquinolone antibiotic. Ofloxacin is bactericidal and its mode of action depends on blocking of bacterial DNA replication by binding itself to an enzyme called DNA gyrase

- which allows the untwisting required to replicate one DNA double helix into two. Notably the drug has 100 times higher affinity for bacterial DNA gyrase than for mammalian. Ofloxacin is a broad-spectrum antibiotic that is active against both Gram-positive and Gram-negative bacteria. Mechanism of action Ofloxacin acts on DNA gyrase and toposiomerase IV

- enzymes which

- like human topoisomerase

- OFLOXACIN 200mg

- ORNIDAZOLE 500mg

- AMOXYCILLIN 200 MG

- POTASSIUM CLAVULANATE 28.5 MG WITH LACTIC ACID BACILLUS Packing:- 1X10 M.R.P: - 260   PHARMACOLOGY PHARMACOKINETICS: ABSORPTION: Dosing in the fasted or fed state has minimal effect on the pharmacokinetics of amoxicillin. While amoxicillin/clavulanate potassium can be given without regard to meals

- absorption of clavulanate potassium when taken with food is greater relative to the fasted state. In one study

- the relative bioavailability of clavulanate was reduced when amoxicillin/clavulanate potassium was dosed after eating something. DISTRIBUTION: Component in amoxicillin/clavulanate potassium is highly protein-bound; clavulanic acid is approximately 25% bound to human serum and amoxicillin approximately 18% bound. Amoxicillin diffuses readily into most body tissues and fluids with the exception of the brain and spinal fluid. METABOLISM AND EXCRETION: The half-life of amoxicillin after the oral administration of amoxicillin/clavulanate potassium is 1.3 hours and that of clavulanic acid is 1 hour. Approximately 50% to 70% of the amoxicillin and approximately 25% to 40% of the clavulanic acid are excreted unchanged in urine during the first 6 hours after administration of a single 250 mg/125 mg or 500 mg/125 mg tablet of amoxicillin/clavulanate potassium.   INDICATIONS: Amoxicillin/clavulanic acid is a penicillin-type antibiotic used to treat a wide variety of bacterial infections. It works by stopping the growth of bacteria. This antibiotic only treats bacterial infections. It will not work for viral infections (e.g.

- AMOXYCILLIN 500 MG

- CLAVULANIC ACID 125 MG Packing: - 1X10 M.R.P: -169   PHARMACOLOGY PHARMACOKINETICS: ABSORPTION: Dosing in the fasted or fed state has minimal effect on the pharmacokinetics of amoxicillin. While amoxicillin/clavulanate potassium can be given without regard to meals

- absorption of clavulanate potassium when taken with food is greater relative to the fasted state. In one study

- the relative bioavailability of clavulanate was reduced when amoxicillin/clavulanate potassium was dosed after eating something. DISTRIBUTION: Component in amoxicillin/clavulanate potassium is highly protein-bound; clavulanic acid is approximately 25% bound to human serum and amoxicillin approximately 18% bound. Amoxicillin diffuses readily into most body tissues and fluids with the exception of the brain and spinal fluid. METABOLISM AND EXCRETION: The half-life of amoxicillin after the oral administration of amoxicillin/clavulanate potassium is 1.3 hours and that of clavulanic acid is 1 hour. Approximately 50% to 70% of the amoxicillin and approximately 25% to 40% of the clavulanic acid are excreted unchanged in urine during the first 6 hours after administration of a single 250 mg/125 mg or 500 mg/125 mg tablet of amoxicillin/clavulanate potassium.   INDICATIONS: Amoxicillin/clavulanic acid is a penicillin-type antibiotic used to treat a wide variety of bacterial infections. It works by stopping the growth of bacteria. This antibiotic only treats bacterial infections. It will not work for viral infections (e.g.

- TRAMADOL HYDROCHLORIDE 37.5mg

- PARACETAMOL 325mg

- DROTAVERINE 80mg

- MEFENAMIC ACID 250mg PACKING: - 10X10 M.R.P: - 750   Drotaverine Drotaverine is an effective spasmolytic drug. Mechanism of Action of Drotaverine Drotaverine has spasmolytic and vasodilating action. It exerts its action by inhibiting phosphodiesterase enzyme IV. This will leads to a decrease in cyclic AMP level and reduction in calcium ions (Ca2+). The reduction of calcium ions will dilates the unstipped muscles and blood vessels strongly and relieves spasm of smooth muscles. Pharmacokinets of Drotaverine Absorption: Drotaverine is rapidly absorbed after oral administration. Distribution: It is widely distributed in protein bound form. Metabolism: Extensively metabolised in the liver. Excretion: It is excreted mainly with the bile. Onset of Action for Drotaverine: -30 minutes Duration of Action for Drotaverine : -4 hours. Half Life of Drotaverine: -7 - 12 hours   Mechanism of Action of Mefenamic Acid: - Mefenamic acid has analgesic

- anti-inflammatory and antipyretic action. It acts by inhibiting Prostaglandin (PGs) synthesis and their release at the site of injury. Prostaglandins cause tenderness and amplify the action of other analgesics. Mefenamic acid inhibits cyclo-oxygenase enzyme and antagonizes prostaglandin actions.   Pharmacokinets of Mefenamic Acid Absorption: Mefenamic acid is well absorbed after oral administration. Distribution: It is distributed in the body in protein bound form. Metabolism: It is metabolised in the liver. Excretion: Mefenamic acid and its metabolites are excreted mainly in the urine. Onset of Action for Mefenamic Acid: - 1-2 hours. Duration of Action for Mefenamic Acid: -6 hours. Half Life of Mefenamic Acid: -2-4 hours

- FEBUXOSTAT 40mg

- AZITHROMYCIN 250mg

- AZITHROMYCIN 500mg

- NIMESULIDE 100mg

- PARACETAMOL 325mg

- DEFLAZACORT 6mg

- ACECLOFENAC 200mg

- ACECLOFENAC 100mg

- PARACETAMOL 325mg

- CHLORZOXAZONE 250mg

- ACECLOFENAC 100mg

- PARACETAMOL 325mg

- ACECLOFENAC 100mg

- PARACETAMOL 325mg

- SERRATIOPEPTIDASE 15mg

- DEFLAZACORT 30MG

- CEFIXIME 200MG Dispersible with LACTOBACILLUS

- OFLOXACIN 200MG + ORNIDAZOLE 500MG

- OFLOXACIN 200MG

- PANTOPRAZOLE 40MG

- NIMESULIDE 100MG + PARACETAMOL 325MG

- MONTELEUKAST 10MG + LEVOCETRIZINE 5MG

- FERROUS ASCORBATE 100 MG + FOLIC ACID 1.5 MG + ZINC 22.5MG

- DEFLAZACORT 6MG

- AMOXYCILLIN 500MG + CLAVULANATE POTT. 125MG

- AMOXYCILLIN 500MG + CLAVULANATE POTT. 125MG + LACTOBACILLUS 60 MILLION SPORES

- DICLOFENAC SODIUM 50MG + SERRATIOPEPTIDASE 10MG

- FLUCONAZOLE 150 MG

- CITICOLINE SODIUM 500MG

- CEFPODOXIME 200MG

- CEFUROXIME 500MG

- AZITHROMYCIN 500MG

- AZITHROMYCIN 250MG

- ACECLOFENAC 100MG + PARA 325MG + SERRATIO 15MG

- ACECLOFENAC 100MG + PARACETAMOL 325MG

- MULTIVITAMIN MULTIMINERAL & ANTIOXIDANTS

- BILASTIN 20MG

- ACEBROPHYLLINE 100 MG + N-ACETYLCYSTEINE 600 MG

- KETOROLAC TROMETHAMINE 10 MG DISPERSIBLE

- BILASTIN 20MG+ MONTELUKAST 10 MG

- COMPOSITION: – TRYPSIN

- CHYMOTRYPSIN (50

- 000 I.U.)

- DICLOFENAC 50MG

- CEFUROXIME 500MG   CEFUROXIME 500 MG: – Cefuroxime Tablets is an antibiotic that is active against a wide range of gram-positive and gram-negative bacteria. It is a cephalosporin antibiotic. It acts by inhibiting bacterial cell wall growth. PHARMACODYNAMICS: – Cefuroxime Tablets is a second-generation cephalosporin

- this works as penicillin. It interrupts the synthesis of the bacterial cell walls by interfering with the formation of major components essential for the formation of cell walls i.e. peptidoglycan. Like penicillins

- Cefuroxime Tablets binds to penicillin-binding proteins in the bacterial cell wall which affects the synthesis of the bacterial cell wall. Ultimately

- Cell lysis is initiated with autolytic enzymes in the cell wall such as autolysins. PHARMACOKINETICS:- ABSORPTION: – The absorption takes place from the GIT. It is observed that absorption is greater in the presence of food. PROTEIN BINDING: – About half of the drug concentration binds to serum protein. METABOLISM: – The metabolized components are acetaldehyde and acetic acid. HALF-LIFE: – On intramuscular or intravenous injection 80 minutes of Half-Life is observed. INDICATIONS: – Cefuroxime Tablets treats different types of bacterial infections like: – Urinary Tract Infections Tonsillitis Gonorrhea Ear infections Bronchitis

- COMPOSITION: – CEFUROXIME AXETIL 500 MG + POTASSIUM CLAVULANATE 125 MG   Carfax-CV comprises cefuroxime which treats a wide variety of infections caused by bacteria. It is a cephalosporin antibiotic and works by inhibiting bacterial cell growth. MECHANISM of ACTION: – CARFAX-CV (CEFUROXIME AXETIL 500 MG + POTASSIUM CLAVULANATE 125 MG) has a broad spectrum of activity against common pathogens. It produces its bactericidal action by inhibiting bacterial cell wall synthesis. Cefuroxime binds to the target proteins which are responsible for bacterial replication. Clavulanic acid is a naturally derived beta-lactamase inhibitor produced by Streptomyces clavuligerus. Clavulanic acid binds to and inactivates them thus preventing the destruction of cefuroxime that is a substrate for this enzyme. INDICATIONS: – CARFAX-CV (CEFUROXIME AXETIL 500 MG + POTASSIUM CLAVULANATE 125 MG)is indicated for the treatment of patients with mild to moderate infections caused by susceptible strains of the designated microorganisms in the conditions listed below: Pharyngitis/tonsillitis Acute bacterial otitis media Acute bacterial maxillary sinusitis Acute bacterial exacerbations of chronic bronchitis and secondary bacterial infections of acute bronchitis Uncomplicated skin and skin structure infections Uncomplicated urinary tract infections Uncomplicated gonorrhea (urethral and endocervical) Early Lyme disease (erythema migrans)

- ETORICOXIB 90 MG   Docru contains the composition of Etoricoxib Tablets which is an anti-inflammatory medicine used to relieve pain

- swelling

- and inflammation in the body. It belongs to the class of drug which is a non-steroidal anti-inflammatory drug (NSAID) that treats the conditions due to arthritis. Etoricoxib Tablets work by decreasing the built-up of prostaglandins

- a chemical reason behind the pain

- IVERMECTIN 12MG

- Ketorolac Tromethamine Dispersible Tablets Ketsog is a composition of Ketorolac Tablet which is prescribed for pain relief. It relieves discomfort in conditions like post-operative problems or pain. Ketorolac tromethamine dispersible tablets are non-steroidal anti-inflammatory drugs (NSAID) that help in barring the discharge of certain chemical messengers that cause pain and inflammation (redness and swelling) in the patient’s body after the post-operative. Precaution for Ketorolac Tromethamine Dispersible Tablets Ketorolac Tromethamine Dispersible Tablets should be taken in the dose and span as advised by the specialist. It should be taken with diet to prevent stomach overthrow. For better results dissolve the tablet in a glass of water before consuming it. Inform the doctor if the patient has any records of heart disease or stroke. Side Effects of Ketorolac Tromethamine Dispersible Tablets Vomiting

- stomach pain

- nausea

- and indigestion are some of the common side effects of Ketorolac Tromethamine Dispersible Tablets. It may also create dizziness

- LEVOCETIRIZINE 5MG + MONTELUKAST 10 MG   Montelukast+Levocetirizine a combined therapy is prescribed for the systemic treatment of allergic reactions such as chronic urticaria

- obstructive airway diseases and rhinitis. Montelukast belongs to leucotriene receptor antagonist. • Montelukast + Levocetirizine is contraindicated in patients with an allergy to either or both drugs

- hepatic impairment

- NSAID allergy

- MO-ZINE KID is a combination of two medicines: Levocetirizine and Montelukast Tablet used for sneezing and runny noses due to sensitivities

- such as Hay fever and Allergic skin conditions. Levocetirizine Tablet belongs to is an Antiallergic drug class that blocks a chemical carrier (histamine) responsible for runny nose

- watery eyes

- and sneezing in the patient due to allergy. Montelukast belongs to a drug class known as leukotriene antagonist. It operates by pressing another chemical messenger (leukotriene). This subdues inflammation (swelling) in the airways and nose and improves signs of allergy. Precaution for Levocetirizine and Montelukast Tablets It is helpful to have plenty of fluids while taking Levocetirizine and Montelukast Tablet. Before the patient starts taking this medicine

- MECOBALAMIN 75 MG & NORTRIPTYLINE 10 MG   Nortriptyline acts by inhibiting the movement of pain signals in the brain as nortriptyline is a tricyclic antidepressant that increases the levels of chemical messengers (serotonin and noradrenaline). Mecobalamin helps in the production of myelin

- this helps to protect nerve fibers and rejuvenates damaged nerve cells. Together

- they relieve neuropathic pain (pain from damaged nerves). PHARMACODYNAMICS Nortriptyline produces anti-depressants. MECOBALAMIN 75 MG & NORTRIPTYLINE 10 MG effect by inhibiting the reuptake of Noradrenaline and Serotonin (5 HT) in the CNS nerve terminals.So that an increased concentration of neurotransmitters in the synaptic cleft is produced. It also possesses central anticholinergic activities. Mecobalamin is a form of vitamin B12 that is neurologically active and it is a water-soluble vitamin in the body. It is a cofactor in the enzyme methionine synthase

- which transfers methyl groups for the regeneration of methionine.   PHARMACOKINETICS Nortriptyline • Absorption: Rapid absorption is observed on oral administration. • Distribution: It is widely distributed in the body in protein-bound form. • Metabolism: The metabolism of Nortriptyline takes place in the liver. • Excretion: In urine and some traces in feces excretion of these molecules can be noticed. Mecobalamin • Absorption: Absorbed after oral

- METHYLPREDNISOLONE 4MG   METHYLPREDNISOLONE :- Methylprednisolone is a synthetic glucocorticoid or corticosteroid drug. It is used to treat conditions such as arthritis

- blood disorders

- severe allergic reactions

- certain cancers

- CEFPODOXIME PROXETIL DISPERSIBLE TABLETS   Cefpodoxime Tablet is an antibiotic used to treat infections caused due to bacteria. As the tablet is an effective range of antibiotics thus it helps in destroying the bacteria by stopping them from forming the bacterial protective covering (cell wall) which is essential for them to survive. Cefpodoxime Proxetil Dispersible Tablets are prescribed to treat infections of the lungs (eg. pneumonia)

- urinary tract

- nasal sinus

- throat

- RIFAXIMIN 400MG

- RIFAMIXIN 550 MG

- COENZYME Q10 50 MG + L-CARNITINE L- TARTRATE 500 MG + LYCOPENE 10 % 5 MCG + ZINC SULPHATE 0.75 MG + VITAMIN E ACETATE 1.5 MG

- DOXOFYLLINE 400 MG TABLET Sofyllin 400mg Tablet contains Doxofylline which is used to treat and prevent symptoms of asthma and chronic obstructive pulmonary disorder that is a lung problem in which the flow of air to the lung is blocked and breathing becomes uncomfortable. Doxofylline tablets help in smoothing the muscles of the air passages

- by expanding them and making it easier to breathe for the person. Chronic obstructive pulmonary disease (COPD) is also known as a chronic lung disorder in which there is a problem in emptying air of the lungs or where there is airflow obstruction. Due to this obstruction

- patients have trouble breathing or get tired easily because they are breathing disorders. Whereas Asthma is a chronic breathing problem that causes issues in the bronchial tubes

- which are responsible to allow air to move in and out of the lungs. When your airways are blocked

- URSODEOXYCHOLIC ACID 300 MG TABLETS   Urowar 300mg Acid tablets are used in the treatment of primary biliary cirrhosis and gallbladder stones. Ursodeoxycholic Acid is the product of bacteria metabolism in the intestine and it is considered as secondary bile acid. There is various type of bile acid which are produced hepatically and subsequently stored in the gallbladder of a person. When the primary bile acids are produced into the large intestine

- they can be broken down into secondary bile acids by bacteria present in the stomach. Ursodeoxycholic acid tablets activate cholesterol levels by slowing the rate at which the intestine can absorb cholesterol and break down micelles

- which have cholesterol. Because of this activity

- ursodeoxycholic acid is the effective treatment for and gallbladder stones. Ursodeoxycholic Acid tablets belong to a hepatoprotective medication that improves liver enzymes

- Multivitamin

- Multimineral & Antioxidant Capsules Vilto consists of Multivitamin

- Multimineral & Antioxidant Tablets that are used for restoring the level of vitamins and minerals that decreased because of unhealthy diet and no proper nutrition daily. These tablets are very much useful as their antioxidant formula with the multivitamin will be very good for your eyes

- brain

- PARACETAMOL IP 650MG   (Paracetamol 650MG)Tablet is used to temporarily relieve fever and mild to moderate pain such as muscle ache

- headache

- toothache

- arthritis

- Nimesulide

- Serritiopeptidase and Paracetamol Tablets Precautions for Nimesulide and Paracetamol Tablets  Nimesulide and Paracetamol Tablets must be swallowed as a whole

- without chewing. It is recommended to be taken with food. The patient should avoid taking alcohol while treatment for this medication. If the patient is pregnant

- breastfeeds

- (ACECLOFENAC 100 MG + THIOCHOLCHISIDE 4 MG)   PHARMACOLOGY PHARMACODYNAMICS OF THIOCOLCHICOSIDE Mechanism of Action: – Thiocolchicide is a GABA-A receptor antagonist

- which binds to GABA-A and strychnine-sensitive glycine receptors. This results from the reduction of spasticity. It also has myorelaxant effects at the supraspinal level

- via complex regulatory mechanisms. PHARMACODYNAMICS OF ACECLOFENAC Mechanism of Action: – It inhibits cyclo-oxygenase (COX) activity and suppresses the PGE2 production by inflammatory cells

- by inhibiting IL-Beta & TNF in the inflammatory cells (Intracellular Action). It blocks degeneration and stimulates the synthesis of the extracellular matrix of cartilages by inhibiting the action of different cytokines. Drugs and their metabolites inhibit IL-6 production by human chondrocytes. This leads to inhibition of increase of inflammatory cells in synovial tissue

- DEXTROMETHORPHAN HYDROBROMIDE 10MG

- PHENYLEPHRINE HYDROCHLORIDE IP 5MG

- CHLOPHENIRAMINE MALEATE IP 2MG   Chlorpheniramine/dextromethorphan is a decongestant

- antihistamine