Pharmaceutical Tablets

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Salvica-OZ Tablets

Each Tablets contains

Cefixime 200 mg

Ornidazole 500 mg

SALVICA-OZ Tablets contains Cefixime and Ornidazole.

It is highly stable in the presence of beta-lactamase enzymes. The antibacterial effect of Cefixime results from inhibition of mucopeptide synthesis in the bacterial cell wall. Cefixime binds to specific penicillin-binding proteins (PBPs) located inside the bacterial cell wall, causing the inhibition of the third and last stage of bacterial cell wall synthesis.

ORNIDAZOLE contains an imidazole ring which bears a nitro group. It is an anti-amoebic agent. Ornidazole has a broad spectrum -cidal activity against Protozoa and some anaerobic bacteria.

Cefixime is an antibiotic, third-generation cephalosporin. Ornidazole belongs to the class of nitroimidazoles.

SALVICA-OZ Tablets are used in the treatment of the following conditions:

• Diarrhea and dysentery
• Abdominal infections
• Dental infections
• Post-surgical infections
• Infections of female reproductive tract

Salvica-OZ (Cefixime Trihydrate 200mg+ Ornidazole 500mg Tablets)

Dosage- 1-2 SALVICA-OZ Tablets once daily or in two divided doses.

Mode of Action-

Cefixime binds to specific penicillin-binding proteins (PBPs) located inside the bacterial cell wall, causing the inhibition of the third and last stage of bacterial cell wall synthesis. Cell lysis is then mediated by bacterial cell wall autolytic enzymes such as autolysins; it is possible that cefixime interferes with an autolysin inhibitor.

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Description

• disclaimer the information given below is for the use of medical sales rep and is not for doctors. Information given below is inadequate for treating a patient

garitel-40 tablet

composition

telmisartan ip 40 mg

telmisartan is a newer type of blood pressure medicine known as an angiotensin ii receptor blocker (arb for short). As the name implies, telmisartan blocks angiotensin ii receptors. This decreases the effectiveness of a chemical known as angiotensin ii, which normally causes blood vessels to narrow (constrict). By blocking the effects of angiotensin ii, telmisartan causes blood vessels to relax.

indications and usage

high blood pressure (hypertension)

drug interaction

Complementry mechanism of action

Reduction in peripheral resistence with arb

Reduction of fluid volume with diuretics

Arbs counteract reactive increase in blood pressure related to diuretic induced renin secretion

Arbs ameliorates diuretic induced potassium depletion

Well tolerated; fewer metabolic disturbances

No significant variation in pharmacokinetic parameters of telmisartan in presence of hydrochloroth.iazide

combination of telmisartan with hydrochlorot.hiazide was found to be more effective than each agent alone in lowering blood pressure. Indeed , combining telmisartan with hydrochlorothia.zide enhances the antihypertensive efficacy of telmisartan in patients not adequately controlled with telmisartan alone.

pharmacokinetic

telmisartan is orally well absorbed and metabolized to an active metabolite which is more potent than losartan as at1 antagonist. Orally administered hydrochlor.othiazide is rapidly absorbed and diuretic effect is seen in 1 hour and their duration lasts up to 12-24 hours. Both telmisartan and hydroc.hlorothiazide has longer duration of actions. These agents are bound to plasma proteins to varying degrees and this has no correlation to their half-life.

pharmacodynamics

the pharmacodynamics of telmisartan & hydrochlo.rothiazide has been investigated in vitro and in vivo in rodents, guinea pigs, rabbits and dogs. The combination of telmisartan with hydroc.hlorothiazide (40 mg/12. 5 mg and 80 mg/12. 5 mg) is expected to benefit patients with hypertension who are not adequately responsive to telmisartan alone.

contraindications

Second and third trimesters of pregnancy.

Biliary obstructive disorders.

Severe hepatic impairment.

storage

this medicinal product does not require any special temperature storage conditions. Store in the original package in order to protect from moisture.

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Mypod 100/200mg Tablets

Cefpodoxime - A third generation cephalosporin .

Prior to initiation of cefpodoxime proxetil therapy, appropriate specimens should be obtained for identification of the causative organism and in vitro susceptibility tests. Cefpodoxime proxetil may be started pending results of susceptibility tests but should be discontinued if the organism is found to be resistant to the drug.

Acute Otitis Media

Pharyngitis and Tonsillitis

Respiratory Tract InfectionsAcute Exacerbations of Chronic Bronchitis

Acute Sinusitis

Community-acquired Pneumonia

Skin and Skin Structure Infections

Urinary Tract Infections

Gonorrhea and Associated InfectionsUncomplicated Gonorrhea

Disseminated Gonococcal Infections

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fenasal-t4/t8 tab

each film coated tablet contains:

aceclofenac ip 100 mg

thiocholchicoside 4/8 mg

aceclofenac is an orally administered phenylacetic acid derivative with effects on a variety of inflammatory mediators. It is from the class of non-steroidal anti-inflammatory drug (nsaid), related to diclofenac. Through its analgesic and anti-inflammatory properties, aceclofenac provides symptomatic relief in a variety of painful conditions.

thiocolchicoside, a semi-synthetic derivative of the naturally occurring compound colchicoside with a relaxant effect on skeletal muscle, has been found to displace both [3h]gamma-amino butyric acid ([3h]gaba) and [3h]strychnine binding, suggesting an interaction with both gaba and strychnine-sensitive glycine receptors.

indications:
anti-inflammatory, analgesic, neck and shoulder pain .

rationale of combination:

product description:
thiocolchicoside, a semi-synthetic derivative of the naturally occurring compound colchicoside and is a muscle relaxant agent with anti-inflammatory and analgesic actions, also is used topically for the treatment of muscular spasms and for rheumatologic, orthopedic, and traumatologic disorders and has been found to displace both [3h] gamma-amino butyric acid ([3h] gaba) and [3h] strychnine binding, suggesting an interaction with both gaba and strychnine-sensitive glycine receptors. Aceclofenac belongs to a group of medicines called non-steroidal anti-inflammatory drugs (nsaids) and of phenyl acetic acid derivative with effects on a variety of inflammatory mediators. It works by blocking the action of a substance in the body called cyclo-oxygenase. Cyclo-oxygenase is involved in the production of various chemicals in the body, some of which are known as prostaglandins. Prostaglandins are produced in response to injury or certain diseases and would otherwise go on to cause pain, swelling and inflammation. Combination of proven nsaid aceclofenac with an effective non sedating muscle relaxant thiocolchicoside to treat painful muscle spasm.

Disclaimer: the information given below is for the use of medical sales rep and is not for doctors. information given below is inadequate for treating a patient

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Each Film Coated Tablet Contains:

Cefpodoxime 200 mg
Dicloxacillin Extended Release 500 mg

Cefpodoxime Proxetil an oral third generation cephalosporin antibiotic. It is commonly used to treat acute otitis media, pharyngitis and sinusitis.

Dicloxacillin Sodium is a narrow-spectrum beta- lactum antibiotic of the penicillin class. It is commonly used in Pneumonia, septic arthritis and throat infections.

Indications:

● Acute otitis media

● Pharyngitis and/or tonsillitis

● Community-acquired pneumonia

● Acute bacterial exacerbation of chronic bronchitis

● Acute, uncomplicated urethral and cervical gonorrhea

● Uncomplicated skin and skin structure infections

● Staphylococcal skin infections and cellulitis – including impetigo, otitis externa, folliculitis, boils, carbuncles, and mastitis.

● Pneumonia (adjunct)

● Osteomyelitis, septic arthritis, throat infections, streptococcus● Septicaemia

● Empirical treatment for endocarditis● Surgical prophylaxis

Rationale for Combination

● Reduction in the frequency of the dosing.

● Increase in the effectiveness of drug by localization at the site of action.● Uniform drug delivery.

● Release of one or more drugs continuously in a predetermined pattern for a fixed period time, either systemically or to a specified target organ.

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DEGOUT-40 (febuxostat) tablet for oral use

INDICATIONS AND USAGE

• DEGOUT-40 is a xanthine oxidase (XO) inhibitor indicated for the chronic management of hyperuricemia in patients with gout.
• DEGOUT-40 is not recommended for the treatment of asymptomatic hyperuricemia.

DOSAGE AND ADMINISTRATION

• DEGOUT-40 is recommended at 40 mg or 80 mg once daily. The recommended starting dose of DEGOUT-40 is 40 mg once daily. For patients who do not achieve a serum uric acid (sUA) less than 6 mg per dL after 2 weeks with 40 mg, DEGOUT-40 80 mg is recommended.
• DEGOUT-40 can be administered without regard to food or antacid use.
• No dose adjustment is necessary when administering DEGOUT-40 to patients with mild to moderate renal or hepatic impairment.

DOSAGE FORMS AND STRENGTHS

• Tablet: 40 mg, 80 mg.

CONTRAINDICATIONS

• DEGOUT-40 is contraindicated in patients being treated with azathioprine, mercaptopurine, or theophylline.

WARNINGS AND PRECAUTIONS

• Gout Flare: An increase in gout flares is frequently observed during initiation of anti-hyperuricemic agents, including DEGOUT-40. If a gout flare occurs during treatment, DEGOUT-40 need not be discontinued. Prophylactic therapy (i.e., non-steroidal anti-inflammatory drug (NSAID) or colchicine upon initiation of treatment) may be beneficial for up to six months.
• Cardiovascular Events: A higher rate of cardiovascular thromboembolic events was observed in patients treated with DEGOUT-40 than allopurinol in clinical trials. Monitor for signs and symptoms of MI and stroke.
• Liver Enzyme Elevation: Transaminase elevations have been observed in DEGOUT-40-treated patients. Monitor liver function tests periodically.

ADVERSE REACTIONS

• Adverse reactions occurring in at least 1% of DEGOUT-40-treated patients, and, at least 0.5% greater than placebo, are liver function abnormalities, nausea, arthralgia, and rash.

DRUG INTERACTIONS

• Concomitant administration of DEGOUT-40 with XO substrate drugs, azathioprine, mercaptopurine, or theophylline could increase plasma concentrations of these drugs resulting in severe toxicity.

USE IN SPECIFIC POPULATIONS

• There is insufficient data in patients with severe renal impairment. No studies have been conducted in patients with severe hepatic impairment. Caution should be exercised in these patients.
• No studies have been conducted in patients with secondary hyperuricemia (including patients being treated for Lesch-Nyhan syndrome or malignant disease, or in organ transplant recipients); therefore, DEGOUT-40 is not recommended for use in these patients.

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Atenolol is a cardioselective beta blocker.
Amlodipine is a dihydropyridine calcium channel blocker that blocks the transmembrane influx of calcium ions into vascular smooth muscle and cardiac muscle.

Pharmacokinetics

Combination of the two drugs results in additive antihypertensive action.

Absorption:

Amlodipine: Plasma levels peak 6-12 hr after oral admin; absolute bioavailability is estimated to be 64-90%.

Atenolol:

Absorption is rapid and consistent but incomplete; about 50% of an oral dose is absorbed in the GI tract; plasma levels peak 2-4 hr after oral admin.

Distribution:

Amlodipine: 93% bound to plasma proteins.

Atenolol: 6-16% bound to plasma proteins.

Metabolism:

Amlodipine: About 90% converted to inactive metabolites hepatically.

Atenolol: Little or no hepatic metabolism.

Excretion:

Amlodipine: 10% of parent compound and 60% of the metabolites are removed in the urine; elimination from the plasma is biphasic with terminal half-life of about 30-50 hr. Atenolol: 50% of the oral dose is removed unchanged in the faeces; absorbed drug is removed mainly via renal elimination; half-life is about 6-7 hr.

Atenolol + Amlodipine Indications / Atenolol + Amlodipine Uses

Antihypertensive activity

Atenolol + Amlodipine Adverse Reactions / Atenolol + Amlodipine Side Effects

Headache, hypotension, dizziness, breathlessness, fatigue, muscle cramps, bradycardia, palpitations, flushing, oedema, dyspnoea, dyspepsia, cold extremities. Drowsiness, chestpain impotence rarely. Hypersensitivity reactions.

Precautions

Overdosage may cause hypotension and less commonly, congestive cardiac failure. Unabsorbed drug may be removed by gastric lavage or use of activated charcoal. Symptomatic treatment may be administered.

Special Precautions

Excessive fall of BP may occur in elderly patients. Caution in patients with COPD, thyrotoxicosis, congestive failure, vasospastic angina, hepatic renal impairment. Caution in diabetic patients as beta-blockers may mask tachycardia occurring with hypoglycaemia. Withdrawal should be gradual. Lactation. Safety and efficacy have not been established in children. Not to be used in untreated phaeochromocytoma.

Other Drug Interactions

Additive effect when used with catecholamine depleting drugs; monitor for hypotension and/or marked bradycardia. If used with clonidine, clonidine withdrawal should occur a few days after withdrawal of the beta-blocker to prevent rebound hypertension; if replacing clonidine by beta-blocker, beta-blocker should be introduced only after clonidine administration has stopped for several days. Concurrent use with prostaglandin synthase inhibiting drugs (e.g. indomethacin) may reduce the hypotensive effects of beta-blockers.

Dosage 

Oral
Chronic stable angina, Hypertension

Adult: Per tablet contains atenolol 25 or 50 mg and amlodipine (as besylate) 5 mg: 1 tab once daily, may increase to 2 tablets daily if needed.

Elderly: Per tablet contains atenolol 25 mg and amlodipine (besylate) 5 mg: Initiate with 1 tablet daily.

Renal impairment: Per tablet contains atenolol 25 mg and amlodipine (besylate) 5 mg: Initiate with 1 tablet daily.

Additional Information:

• Pay Mode Terms: T/T (Bank Transfer)

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Each Film Coated Tablet Contains:
Etoricoxib 60 mg
Paracetamol 325 mg
Before knowing its combination, we should need to know that how they work individually, so you know that Etoricoxib is Anti-inflammatory medicines NSAID used to treat rheumatoid, arthritis, Gout and osteoarthritis and Paracetamol is also NSAID and it is used to relieve mild to moderate aches and pains associated with conditions such as headaches, migraine, toothache, teething, colds and flu. It is also useful for reducing fever.
It has been demonstrated by recent studies concomitant administration of Etoricoxib and Paracetamol shows better symptoms relief compared with modest improvement of mild to moderate pain, inflammation and fever.

Indication and Usage:
Combination of Etoricoxib and Paracetamol used to treat:
Mild to moderate pain for example headaches, muscle aches, arthritis, backache, toothache or the symptoms of a cold.
Control a fever(high temperature, also known as pyrexia) – for example, when someone has the flu (influenza).
It is also used for the treatment of Rheumatoid arthritis, Gout and osteoarthritis.

Pharmacokinetics:
It is readily absorbed from the gastrointestinal tract with peak plasma concentrations occurring about 10 to 60 minutes after oral administration. It is distributed into most body tissues. Plasma protein binding is negligible at usual therapeutic doses but increases with increasing doses. The elimination half-life varies from about 1 to 3 hours.
It is metabolised extensively in the liver and excreted in the urine mainly as inactive glucuronide and sulfate conjugates. Etoricoxib selectively inhibits isoform 2 of cyclo-oxigenase enzyme (COX-2).

Pharmacodynamics:
Paracetamol is a p-aminophenol derivative that exhibits analgesic and antipyretic activity. It does not possess anti-inflammatory activity. Paracetamol is thought to produce analgesia through a central inhibition of prostaglandin synthesis.

Mode of Action:
Paracetamol works as a painkiller by affecting chemicals in the body called prostaglandins. Prostaglandins are substances released in response to illness or injury. Paracetamol blocks the production of prostaglandins, making the body less aware of the pain or injury. Paracetamol reduces temperature by acting on the area of the brain that is responsible for controlling temperature. Etoricoxib selectively inhibits isoform 2 of cyclo-oxigenase enzyme (COX-2). This reduces prostaglandins (PGs) generation from arachidonic acid.

Drug Interactions:
BEFORE TAKING THIS MEDICINE TELL THE DOCTOR ABOUT ANY MEDICAL PROBLEMS AN ALLERGIES THAT CHILD HAS NOW OR HAS HAD.
Usually drug interactions occur when it is taken with another drug or with food. Before you take a medication for a particular ailment, you should inform the health expert about intake of any other medications including non-prescription medications in this combination of etoricoxib and Paracetamol Risk of side effects increased with concomitant use of , ciclosporin.

Side effects:
Side effects of Etoricoxib and Paracetamol are most likely to be minor like:
Constipation
Swelling of your face, lips, tongue
Nausea

Contraindications:
Caution when used during pregnancy.
Contraindicated in lactation.
Caution in active peptic ulceration, and cerebrovascular disease.

Storage:
Store in cool and dry place.

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We also have the expertise to provide our clients with a wide variety of Olanzapine Tablets. We also test these products as per the international standards of quality before it is finally dispatched to the clients. Customizing the packed quantities of these products as per the demands and specifications of the clients is our special forte.

Features:

• Quick response

• Precise composition

• Longer shelf life

• Zero side effects

• High purity

• High effectiveness

Uses:

• Olanzapine is used to treat schizophrenia and manic episodes in patients with bipolar disorder.

• It is an atypical anti-psychotic, sometimes known as a neuroleptic. Atypical anti-psychotics may be better tolerated than other antipsychotics with a fewer side effects of abnormal movements. Olanzapine is also an anti-manic and mood stabilizing agent.

• It is used to control symptoms of agitation and disturbing behavior associated with mania and schizophrenia. The symptoms of mania include feeling high, having excessive amounts of energy and sometimes being very irritable. Symptoms of schizophrenia include hallucinations (hearing, seeing or sensing things which are not there), abnormal thoughts (mistaken beliefs, unusual suspiciousness) and becoming withdrawn.

Specification:

• Composition: Olanzapine

Additional Information:

• Pay Mode Terms: T/T (Bank Transfer)

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We are making our name in offering the nation with a series of affordable and innovative medicines for a healthier living, for all. We are here presenting a range of Pharma PCD, Pharma Franchise, Pharmaceutical Capsules, Pharmaceutical Tablets, Soft Gel Capsules, Pharmaceutical Syrups, Dry Syrups, Pharmaceutical Injections and Pharmaceutical Drops.

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Description:

• We are also the leading trader and supplier of a huge range of Levofloxacin Tablets 500 Mg. These products are offered to our clients in varied packaging quantities as per their needs and guidelines. Tested in accordance to the international standards of quality, these products are very pure and have a long life span.

Features:

• Quick response
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• Longer shelf life
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Specification:

• Composition: Levofloxacin

Uses:

• Treatment to Prevent Anthrax following Exposure to Disease
• Acute Inflammation of the Maxillary Sinus
• Acute Maxillary Sinus S. Pneumoniae Bacteria Infection
• Acute Maxillary Sinus H. Influenzae Bacteria Infection
• Acute Maxillary Sinus M. Catarrhalis Bacteria Infection
• Pneumonia caused by Pneumococcus Bacteria
• Bacterial Pneumonia caused by Haemophilus Influenzae, Pneumonia due to the Bacteria Haemophilus Parainfluenzae, Bacterial Pneumonia caused by Strep
• Bacterial Pneumonia caused by Staphylococcus
• Pneumonia due to Methicillin-Sensitive

Information provided at this web site is of a general nature and is not intended to take the place of a physician's advice. It is vital that persons diagnosed with, or suspected of having, any disease consult with their physician to assure proper evaluation, treatment and interpretation of information contained on this site.

Additional Information:

• Item Code: Salcult-500-Tablet

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Garispas-DS Tab

Each tablet contains:

Composition:

Dicyclomine ....................................................................20 mg

Mefenamic acid............................................................500 mg

Indication:

Adjunct in gastrointestinal disorders characterised by smooth muscle spasm. As urinary antispasmodic, renal colics, spasmodic dysmenorrhoea.

Description:

Action is achieved via a dual mechanism: (1) a specific anticholinergic effect (antimuscarinic) at the acetylcholine-receptor sites and (2) a direct effect upon smooth muscle (musculotropic).

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Description:

• We are known as the leading trader, supplier and distributor of Lornoxicam Tablets. These products are packed in customized quantities as per the requirements and needs of clients. These products are tested as per international standards of quality to ensure better quality outputs.

Features:

• Quick response
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• Longer shelf life
• Zero side effects
• High purity
• High effectiveness

Each Tablet Contains:

• Lornoxicam 8 mg

Other details:

• Inflammation and pain are the integral part of surgical/ non surgical trauma and many diseases. Lornoxicam is a non steroidal anti-inflammatory drug with analgesic properties and belongs to the class of oxicams

• Lornoxicam inhibits the prostaglandin synthesis by inhibiting COX-1/COX-2 system. It also inhibits the production of pro-inflammatory cytokines TNF-alpha, IL-1beta, IL-6, and IL-8 and the inducible no synthase. It is safe for longer duration and has less side effects

Indications:

• Pain relief
• Rheumatoid arthritis
• Osteoarthritis
• Low back pain
• Post operative pain management
• Gynecological surgery: Hysterectomy
• General surgery

Absorption:

• Extensively absorbed from the GI tract. Peak plasma concentration within 1-2 hours (oral) or 25 min (IM)

Distribution:

• 99% bound to plasma proteins

Metabolism:

• Metabolised to its inactive metabolite

Excretion:

• Excreted in the faeces (as metabolites) and urine (as unchanged drug). Mean elimination half life of 3-4 hours

Additional Information:

• Item Code: Lorkad-8-Tablets

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We are highly appreciated by the clients for manufacturing and supplying Cardio Diabetic Drugs. Moreover, the plates offered by us are tested on various parameters so as to ensure their high purity. Tested as per the international standards of quality, these products are in high demand in the market.
Features:

Quick response

Precise composition

Longer shelf life

Zero side effects

High purity

High effectiveness

Uses:

Glykad 62 Tablets are indicated as an adjunct to diet and exercise to improve glycemic control in adults with type 2 diabetes mellitus.

Specification:

Composition: Metformin 1000 mg, Glimepride 2 mg.

Information provided at this web site is of a general nature and is not intended to take the place of a physician's advice. It is vital that persons diagnosed with, or suspected of having, any disease consult with their physician to assure proper evaluation, treatment and interpretation of information contained on this site.

Additional Information:

• Item Code: Glykad-Tablets

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Telmisartan and amlodipine is a combination of medicines that may be used alone or with other medicines to treat high blood pressure (hypertension). High blood pressure adds to the workload of the heart and arteries. If it continues for a long time, the heart and arteries may not function properly. This can damage the blood vessels of the brain, heart, and kidneys, resulting in a stroke, heart failure, or kidney failure. Lowering blood pressure can reduce the risk of strokes and heart attacks.

Telmisartan is an angiotensin II receptor blocker (ARB). It works by blocking a substance in the body that causes blood vessels to tighten. As a result, the blood vessels relax and this decreases blood pressure. When blood pressure is lowered, the amount of blood and oxygen that go to the heart is increased.

Amlodipine is a calcium channel blocker (CCB). It affects the movement of calcium into the cells of the heart and blood vessels. As a result, amlodipine relaxes the blood vessels and increases the supply of blood and oxygen to the heart while reducing its workload.

This medicine is available only with your doctor's prescription.

This product is available in the following dosage forms:

· Tablet

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We, Salveo Lifecare, are engaged in trading and supplying a broad range of Pantoprazole with Domperidone Tablets.

We are making our name in offering the nation with a series of affordable and innovative medicines for a healthier living, for all. We are here presenting a range of Pharma PCD, Pharma Franchise, Pharmaceutical Capsules, Pharmaceutical Tablets, Soft Gel Capsules, Pharmaceutical Syrups, Dry Syrups, Pharmaceutical Injections and Pharmaceutical Drops.

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Description:
Salof-MS has in vitro activity against a broad spectrum of gram-positive and gram-negative aerobic and anaerobic bacteria. Ofloxacin is thought to exert a bactericidal effect on susceptible microorganisms by inhibiting DNA gyrase, an essential enzyme that is a critical catalyst in the duplication, transcription, and repair of bacterial DNA.Ofloxacin has been shown to be active against most strains of the following microorganisms both in vitro and in specific clinical infections.
Gram-positive Aerobes:
Staphylococcus aureus, Streptococcus pneumoniae, and Streptococcus pyogenes.
Gram-negative Aerobes:
Citrobacter diversus, Enterobacter aerogenes, Escherichia coli, Haemophilus influenzae, Klebsiella pneumoniae, Neisseria gonorrhoeae, Proteus mirabilis, Pseudomonas aeruginosa
Other:
Chlamydia trachomatis.Ornidazole is a 5-nitroimidazole derivative with actions similar to Metronidazole and Tinidazole and is used in the treatment of susceptible Protozoal Infections and also in Anaerobic Bacterial Infections.It is effective against Protozoa including Entamoeba histolytica, Giardia lambia and Trichomonas spp and Bacteria such as Bacteriodes spp., Anaerobic cocci, Fusobacterium spp., Clostridum spp., and Gardenerlla vaginalis. It acts by damage of DNA strands or inhibition of their synthesis.Both Ofloxacin and Ornidazole are almost completely absorbed from the small intestine when administered orally both having almost 100% bioavailability. Subsequent plasma concentrations of Ofloxacin are obtained in 1-2 hours after oral administration. Peak plasma concentrations of Ornidazole are obtained within 2 hours of administration.The plasma elimination of Ornidazole is 12 to 15 hours and less than 15% is bound to plasma proteins. It is widely distributed in body tissues and fluids. Ornidazole is metabolised in the liver and is excreted in the urine mainly as metabolites and conjugates and to a lesser extent in the faces.
Indications:
Salof-OZ is indicated for the treatment of a wide variety of infections caused by susceptible gram-positive and gram-negative organisms along with anaerobes and protozoa. Gynaecological infections including prophylaxis in gynaecological surgeries. Surgical prophylaxis and surgical wound infections. Respiratory tract infections like lung abscess, aspiration pneumonia, empyema and bronchiectasis. ENT infections like chronic sinusitis, chronic suppurative otitis media, cholesteatoma and mastoiditis. Orofacial and dental infections.Dermatological infections like cellulitis, breast and other cutaneous abscesses, angrene, diabetic and decubitus ulcers.Intra-abdominal infections and diarrhoeas of mixed bacterial and protozoal origin.
Dosage:
The usual adult dose is one tablet of Salof-OZ twice a day. The doses may be increased in severe infections. The duration of treatment depends upon the type and severity of infection.
Contraindications:
Hypersensitivity to the quinolone group or the nitroimidazole group of compounds and in those patients with a history of blood dyscrasias.
Other Details:
Each 5 ml contain
Ofloxacin 50mg
Ornidazole 125 mg

Additional Information:

• Item Code: Salof-OZ_Susp

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We, Salveo Lifecare, are engaged in trading and supplying a broad range of Doxylamine Succinate, Pyridoxine Hydrochloride,Folic Acid Tablets.

We are making our name in offering the nation with a series of affordable and innovative medicines for a healthier living, for all. We are here presenting a range of Pharma PCD, Pharma Franchise, Pharmaceutical Capsules, Pharmaceutical Tablets, Soft Gel Capsules, Pharmaceutical Syrups, Dry Syrups, Pharmaceutical Injections and Pharmaceutical Drops.

As an integrated healthcare solutions provider, we cater to several therapeutic areas. We have also established a cordial relations with reliable vendors from whom we procure the range. Moreover, our agents, Pharma Franchise, Pharma PCD ensure that these are processed using quality ingredients and advanced manufacturing techniques. Our pharmaceutical products are quality tested on different parameters to ensure these are in compliance with the WHO-GMP standards. All our medicines are highly effective and do not have any side effects.

We are looking for Pharma PCD & Pharma franchisee queries from all over India.

Additional Information:

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