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Travatan (Travoprost) - Side Effects and Adverse Reactions

 
 



ADVERSE REACTIONS

The most common ocular adverse event observed in controlled clinical studies with TRAVATAN® Ophthalmic Solution 0.004% was ocular hyperemia which was reported in 35 to 50% of patients. Approximately 3% of patients discontinued therapy due to conjunctival hyperemia.

Ocular adverse events reported at an incidence of 5 to 10% included decreased visual acuity, eye discomfort, foreign body sensation, pain, and pruritus.

Ocular adverse events reported at an incidence of 1 to 4% included abnormal vision, blepharitis, blurred vision, cataract, cells, conjunctivitis, dry eye, eye disorder, flare, iris discoloration, keratitis, lid margin crusting, photophobia, subconjunctival hemorrhage, and tearing.

Nonocular adverse events reported at a rate of 1 to 5% were accidental injury, angina pectoris, anxiety, arthritis, back pain, bradycardia, bronchitis, chest pain, cold syndrome, depression, dyspepsia, gastrointestinal disorder, headache, hypercholesterolemia, hypertension, hypotension, infection, pain, prostate disorder, sinusitis, urinary incontinence, and urinary tract infection.



REPORTS OF SUSPECTED TRAVATAN SIDE EFFECTS / ADVERSE REACTIONS

Below is a sample of reports where side effects / adverse reactions may be related to Travatan. The information is not vetted and should not be considered as verified clinical evidence.

Possible Travatan side effects / adverse reactions in 70 year old female

Reported by a individual with unspecified qualification from United States on 2011-10-26

Patient: 70 year old female

Reactions: Anxiety, Nasal Cavity Cancer, Muscular Weakness, Depression, Influenza

Suspect drug(s):
Travatan
    Indication: Glaucoma

Nexium
    Administration route: Oral



Possible Travatan side effects / adverse reactions in 72 year old female

Reported by a consumer/non-health professional from United States on 2011-10-27

Patient: 72 year old female weighing 49.9 kg (109.8 pounds)

Reactions: Weight Decreased, Drug Effect Decreased, Glaucoma, Nausea, Osteoporosis, Eructation, Nervousness

Suspect drug(s):
Travatan
    Dosage: ophthalmic
    Indication: Glaucoma

Prevacid
    Dosage: 15 mg, 1 in 1 d, per oral
    Administration route: Oral
    Indication: Nausea
    Start date: 2000-01-01

Prevacid
    Dosage: 15 mg, 1 in 1 d, per oral
    Administration route: Oral
    Indication: Eructation
    Start date: 2000-01-01

Actonel
    Dosage: 35 mg, 1 in 1 wk, per oral ; 35 mg, 1 in 1 wk, per oral
    Administration route: Oral
    Indication: Osteoporosis
    Start date: 2011-03-01
    End date: 2011-04-01

Actonel
    Dosage: 35 mg, 1 in 1 wk, per oral ; 35 mg, 1 in 1 wk, per oral
    Administration route: Oral
    Indication: Osteoporosis
    Start date: 2008-06-01
    End date: 2010-06-01

Other drugs received by patient: Unknown Anti-Anxiety Medication (Anxiolytics); Zocor (All Other Therapeutic Products); Xalatan; Synthroid



Possible Travatan side effects / adverse reactions in 63 year old male

Reported by a health professional (non-physician/pharmacist) from United Kingdom on 2011-11-16

Patient: 63 year old male

Reactions: Visual Acuity Reduced, Cystoid Macular Oedema

Suspect drug(s):
Travatan

Other drugs received by patient: Antibiotics; Omeprazole; Rifampicin



See index of all Travatan side effect reports >>

Drug label data at the top of this Page last updated: 2006-05-16

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