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Dynapar

Dynapar

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Dynapar
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Dynapar

Category:
Composition: Diclofenac Sodium
Strength: 25 mg/ ml

Description:

DYNAPAR contains diclofenac sodium, a nonsteroidal anti-inflammatory drug (NSAID) known for its analgesic, anti-inflammatory, and antipyretic properties. It works by inhibiting cyclooxygenase (COX-1 and COX-2) enzymes, thereby reducing the synthesis of prostaglandins, which are mediators of pain and inflammation.

Treatment of mild to moderate pain, including postoperative pain and acute musculoskeletal injuries.
Management of inflammatory disorders such as rheumatoid arthritis, osteoarthritis, and ankylosing spondylitis.

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Description

Dosage and Administration

Administration Route:
Intramuscular (IM) injection.​

Use the minimum effective dose for the shortest duration consistent with individual patient treatment goals. Transition to oral NSAIDs as soon as feasible. ​

Note:
Dosage may vary based on individual patient needs and clinical judgment.​

  • Nausea and vomiting​
  • Diarrhea or constipation​
  • Headache​
  • Dizziness​
  • Pain or irritation at the injection site​
  • Gastrointestinal Bleeding:
    Signs include severe stomach pain, black or tarry stools, and vomiting blood.​
  • Hypersensitivity Reactions:
    Such as difficulty breathing, swelling of the face or throat, and skin rashes.​
  • Gastrointestinal Risk:
    NSAIDs, including diclofenac, may cause an increased risk of serious gastrointestinal adverse events, including bleeding, ulceration, and perforation of the stomach or intestines. ​
  • Renal Effects:
    Long-term administration of NSAIDs has resulted in renal papillary necrosis and other renal injury. ​
  • Hypersensitivity:
    Diclofenac is contraindicated in patients with known hypersensitivity to diclofenac. ​
  • Pregnancy and Lactation:
    Use during pregnancy, particularly in the third trimester, is not recommended due to potential adverse effects on the foetus. Caution is advised when administering to nursing women. ​
  • Elderly Patients:
    Elderly patients are at greater risk for serious gastrointestinal events. Use the lowest effective dose for the shortest duration possible.