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Generic name: Aceclofenac

Brand name:

AIRTAL (Highnoon laboratories)

ALKERIS ( Sami pharma)

FLAMIN ( Pulse pharma)

Chemical class: Phenylacetic acid derivative

Therapeutic class: NSAID ; antipyretic; nonnarcotic analgesic

Dosage form:

Tab 100 mg

Inj 1*5

Indication: Pain and inflammation in rheumatoid arthritis, osteoarthritis and ankylosing spondylitis.Conditions involving dental and gynecological pain Symptomatic treatment of pain and inflammation in post traumatic pain, cervical pain, low-back pain, migraine.

Dose:

By Mouth: 

Adult: Maximum recommended dose is 200mg taken as preparation of 100 mg bid, before or after a meal

Child: Not recommended

By injection:

AdultMaximum recommended dose is 200mg taken as preparation of 100mg bid, before or after a meal

Child: Not recommended

Contraindication

Active gastrointestinal bleeding

 active gastrointestinal ulceration

 cerebrovascular disease-history of gastrointestinal perforation related to previous NSAID therapy

 history of recurrent gastrointestinal hemorrhage (two or more distant episode ).history of recurrent gastrointestinal ulceration (two or more distinct episode ) ischemic. , Heart disease, mild heart failure, peripheral arterial disease. Severe heart failure

Cautions: Allergic disorder avoid in acute porphyrias, cardiac impairment (NSAIDs may impair renal function ). Coagulation defects. Connective tissue disorders. Crohn’s disease (maybe exacerbated ) elderly (history  of serious side effect and fatalities) history of cardiac failure hypotension left ventricular dysfunction, edema, risk factor for cardiovascular events, ulcerative colitis ( maybe exacerbated)

Side effects:

Rare Alveolitis – aseptic meningitis ( patient with connective- tissue disorders such as systemic lupus erythematosus maybe especially susceptible) hepatic damage, interstitial fibrosis associated with NSAIDs can lead to renal failure, pancreatitis, papillary necrosis associated with NSAIDs can lead to renal failure. Pulmonary eosinophilia, Stevens- Johnson syndrome.Toxic epidermal necrolysis, visual disturbances

Frequency not known Angioedema, blood disorders, bronchospasm, colitis (induction od or exacerbation of )

Crohn’s disease ( induction of or exacerbation of )

Depression, drowsiness, fluid retention (Rarely precipitating congestive heart failure ) gastrointestinal bleeding, gastro intestinal disturbance,gastro-intestinal ulceration, haematuria, headache, hearing, disturbances, nervousness, hypersensitivity reactions, insomnia, nausea, nervousness, photosensitivity, raised blood pressure, rashes, renal failure (especially in patients with preexisting renal impairment), tinnitus, vertigo.

Pregnancy: Most manufacturers advise avoiding the use of NSAIDs during pregnancy

Breast Feeding: Use with caution during breast-feeding

Hepatic Impairment: Initially 100 mg daily. Use with caution; there is an increased risk of gastrointestinal bleeding and fluid retention. Avoid in severe liver disease.

Renal impairment: The lowest effective dose should be used for the shortest possible duration. Avoid if possible or used for the shortest possible duration. Avoid if possible or use with caution, avoid in moderate to severe impairment.

In Real impairment monitor renal function; sodium and water retention may occur and renal function may deteriorate, possibly leading to renal failure.