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TRAVATAN (TRAVOPROST): ADVERSE REACTIONS
Clinical Studies Experience
Because clinical studies are conducted under widely varying conditions, adverse reaction rates observed in the clinical studies of a drug cannot be directly compared to rates in the clinical studies of another drug and may not reflect the rates observed in practice.
The most common adverse reaction observed in controlled clinical studies with Travoprost (Travatan and Travatan-Z) eye drops 0.004% was ocular hyperemia which was reported in 30 to 50% of patients. Up to 3% of patients discontinued therapy due to conjunctival hyperemia. Ocular adverse reactions reported at an incidence of 5 to 10% in these clinical studies included decreased visual acuity, eye discomfort, foreign body sensation, pain and pruritus.
Ocular adverse reactions reported at an incidence of 1 to 4% in clinical studies with Travatan or Travatan-Z included blepharitis, abnormal vision, blurred vision, conjunctivitis, cataract, corneal staining, iris discoloration, dry eye, keratitis, ocular inflammation, lid margin crusting, photophobia, subconjunctival hemorrhage and tearing.
Nonocular adverse reactions reported at an incidence of 1 to 5% in these clinical studies were angina pectoris, allergy, anxiety, back pain, arthritis, bradycardia, chest pain, bronchitis, cold / flu syndrome, dyspepsia, depression, gastrointestinal disorder, hypercholesterolemia, headache, hypertension, infection, hypotension, pain, sinusitis, prostate disorder, urinary incontinence and urinary tract infections.
Buy Travatan (Travoprost) Online
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