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Osteoace-SP Tablet

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Prescription Required

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Aspen Pharma

Salt Composition

Aceclofenac (100mg) + Paracetamol (325mg) + Serratiopeptidase (15mg)

Overview Osteoace-SP Tablet

Combiflame tablets provide relief from pain and inflammation affecting muscles, joints, and post-surgical sites. This medication effectively manages discomfort and swelling in conditions such as rheumatoid arthritis, ankylosing spondylitis, and osteoarthritis. Dosage and duration should strictly adhere to your physician's instructions. To minimize stomach irritation, administer with food or milk. Consistent, timely intake optimizes therapeutic effects; continue treatment as prescribed until your doctor advises otherwise. Potential side effects include nausea, vomiting, abdominal pain, dyspepsia, heartburn, elevated liver enzymes, vertigo, somnolence, and diarrhea. For extended therapy, your doctor may monitor kidney and liver function, along with blood counts. Prolonged use carries risks of gastrointestinal bleeding and renal complications. Combiflame tablets are contraindicated during pregnancy and lactation.

Uses of Osteoace-SP Tablet

Analgesia

Major Benefits of Osteoace-SP Tablet:

Consume this medication precisely as your physician directs, adhering to the prescribed dosage and timeframe. Ingest the tablet whole; avoid chewing, crushing, or fracturing it. Osteoace-SP Tablets should be administered with a meal.

Common Side effects of Osteoace-SP Tablet:

  • Nausea
  • Vomiting
  • Stomach pain
  • Indigestion
  • Heartburn
  • Loss of appetite
  • Diarrhea
  • Dizziness
  • Increased liver enzymes
  • Drowsiness

How to use Osteoace-SP Tablet:

Consume this medication precisely as your physician directs, adhering to both the prescribed dosage and treatment period. Ingest the tablet whole; avoid chewing, crushing, or fracturing it. Osteoace-SP Tablets should be administered with a meal.

How Osteoace-SP Tablet works:

Osteoace-SP tablets contain aceclofenac, paracetamol, and serratiopeptidase, three active ingredients working synergistically. Aceclofenac, a non-steroidal anti-inflammatory drug (NSAID), and the antipyretic paracetamol, both reduce pain and fever by inhibiting the production of inflammatory mediators. Serratiopeptidase, a proteolytic enzyme, aids tissue repair by selectively degrading damaged proteins at inflamed sites.

SAFETY ADVICE

AlcoholAlcoholUNSAFE

Consuming alcohol alongside Osteoace-SP Tablet is contraindicated.

PregnancyPregnancyCONSULT YOUR DOCTOR

The use of Osteoace-SP Tablets during pregnancy may pose risks. While human research is scant, animal studies indicate potential harm to the fetus. A physician will assess the potential benefits against any risks prior to prescribing. Always seek medical advice.

Breast feedingBreast feedingCONSULT YOUR DOCTOR

Data on Osteoace-SP Tablet use while breastfeeding is lacking. Seek medical advice from your physician.

DrivingDrivingUNSAFE

Taking Osteoace-SP Tablets might reduce attentiveness, impair vision, or induce drowsiness and dizziness. Driving should be avoided if these effects are experienced.

KidneyKidneyCAUTION

Patients with kidney impairment should use Osteoace-SP Tablets cautiously, potentially requiring dosage modification. A physician's consultation is advised. Osteoace-SP Tablets are contraindicated for individuals with severely compromised kidney function.

LiverLiverCAUTION

Individuals with liver impairment should use Osteoace-SP Tablets cautiously, potentially requiring dosage modification under medical supervision. Osteoace-SP Tablets are contraindicated in patients experiencing severe or active liver disease.

What if you forget to take Osteoace-SP Tablet :

Should you forget to take your Osteoace-SP Tablet, administer it at your earliest convenience. Nevertheless, if your next scheduled dose is imminent, omit the missed dose and resume your usual dosing regimen. Avoid taking a double dose.

Facts to Know About Osteoace-SP Tablet

LabelValue
Potential for Dependence None.
Type of Treatment Pain relievers

FAQs on Osteoace-SP Tablet

This formulation unites aceclofenac, paracetamol, and serratiopeptidase to alleviate pain and inflammation. Its mechanism involves reducing the concentration of pain- and inflammation-inducing compounds within the body.
This medication is generally well-tolerated. Nevertheless, some individuals may experience adverse reactions including nausea, vomiting, abdominal discomfort, heartburn, or diarrhea. Promptly contact your physician should any medication-related issue persist.
This medication is typically prescribed for short-term use and may be stopped once your pain subsides. Nevertheless, continued use should follow your physician's instructions.
Nausea and vomiting are potential side effects of this medication. If nausea occurs, consume the medicine with milk, food, or an antacid. Avoid high-fat foods while taking this medication. If vomiting develops, replenish fluids by sipping small amounts of water or other liquids frequently. Persistent vomiting accompanied by dehydration symptoms, such as dark, concentrated urine, infrequent urination, or strong urine odor, warrants immediate medical consultation. Always consult your doctor before taking any other medications concurrently.
Dizziness, including faintness, weakness, unsteadiness, or lightheadedness, is a potential side effect of this medication for some individuals. Should dizziness or lightheadedness occur, rest is recommended until symptoms subside.
This medication is contraindicated in individuals with hypersensitivity to any of its constituents or inactive ingredients, or to other nonsteroidal anti-inflammatory drugs (NSAIDs). Patients with a history of peptic ulcers or those experiencing active or recurrent ulceration/bleeding should generally not use this medicine. Similarly, its use is discouraged in patients with a history of congestive heart failure, hypertension, or hepatic or renal impairment.
This medication is compatible with vitamin B-complex supplements. It provides pain relief, and the vitamin B-complex may address any underlying vitamin deficiency contributing to your condition.
Chronic use of this medication may result in kidney impairment. Healthy kidneys naturally produce prostaglandins, chemicals that offer protective effects. Pain relievers reduce prostaglandin levels, increasing the risk of kidney damage with prolonged use. Individuals with pre-existing kidney conditions should avoid these pain relievers.
Exceeding the prescribed dosage may heighten the likelihood of adverse reactions. Should your pain worsen or fail to respond to the recommended amount, seek medical advice for reassessment.
Retain this medication within its original, sealed packaging. Follow the storage guidelines printed on the package or label. Discard any remaining medication. Prevent access by children, pets, and others.
Osteoace-SP Tablet
57
MRP 70
18% off