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Indication & Dosage
 
 
Oral
SHORT-TERM MANAGEMENT OF MODERATE TO SEVERE POSTOPERATIVE PAIN
Adult:

As trometamol: 10 mg every 4-6 hr. Max dose: 40 mg/day. Max duration: 7 days.

Elderly: 10 mg every 6-8 hr. Max dose: 40 mg/day. Max duration: 7 days.

 
Parenteral
SHORT-TERM MANAGEMENT OF MODERATE TO SEVERE POSTOPERATIVE PAIN
Adult: As trometamol: 10 mg IM/IV followed by 10-30 mg every 4-6 hr if necessary. Max: 90 mg/day (60 mg/day in patients weighing <50 kg). Elderly: Max: 60 mg/day.
Max Dosage:  Max dose: 60 mg/day.
 
Ophthalmic
RELIEF OF OCULAR ITCHING ASSOCIATED WITH SEASONAL ALLERGIC CONJUNCTIVITIS
Adult: As trometamol: Instil 1 drop of a 0.5% solution into the affected eye/s 4 times daily.
 
Ophthalmic
PREVENTION AND RELIEF OF POSTOPERATIVE EYE INFLAMMATION
Adult: As trometamol: Instil 1 drop of a 0.5% solution into the appropriate eye/s 4 times daily starting 24 hr after surgery. Continue for 2 wk.
 
Ophthalmic
PREVENTION AND RELIEF OF POSTOPERATIVE CYSTOID MACULAR OEDEMA ASSOCIATED WITH CATARACT EXTRACTION
Adult: As trometamol: Instil 1-2 drops of a 0.5% solution into the appropriate eye/s every 6-8 hr starting 24 hr before surgery and continue for 3-4 wk after surgery.
 
Ophthalmic
ACTIVE TREATMENT OF CHRONIC APHAKIC OR PSEUDOPHAKIC CYSTOID MACULAR OEDEMA
Adult: s trometamol: Instil 1-2 drops of a 0.5% solution into the affected eye/s 4 times daily for 2-3 mth.
 
Oral
REDUCTION OF OCULAR PAIN AND PHOTOPHOBIA IN PATIENTS UNDERGOING INCISIONAL REFRACTIVE SURGERY
Adult: As trometamol: Instil 1 drop of a 0.5% solution 4 times daily into the operated eye for up to 3 days after surgery.
   
Administration Should be taken with food. (Take immediately after meals.)
   
Precautions Elderly, patients weighing <50 kg, hepatic dysfunction, heart failure, predisposition to reduced blood volume or renal blood flow. Mild renal impairment; monitor renal function closely.
   
Potentially Life-threatening 
Adverse Drug Reactions
GI ulcer, bleeding and perforation, drowsiness, rash, bronchospasm, hypotension, psychosis, dry mouth, fever, bradycardia, chest pain, dizziness, headache, sweating, oedema, pallor, liver function changes. Transient stinging and local irritation (ophthalmic).
   
Adverse Drug Reactions Anaphylaxis. Severe skin reactions. MI, stroke, GI bleeding.
   
Interactions May reduce effects of antihypertensives (e.g. ACE inhibitors or angiotensin II receptor antagonists). Increased risk of renal toxicity with ACE inhibitors, diuretics. Increased adverse effects with aspirin or other NSAIDs. Hallucinations may occur when used with fluoxetine, thiothixene, alprazolam
   
   
 

 

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