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From simple mix-ups to fatal overdoses, medication mistakes happen, on average, once a day to every hospital patient, a new report says. Nationwide, at least 1.5 million people annually are harmed from drug errors, more than half of them in nursing homes.
Many Unfavorable Drug Studies Aren’t Published. Nearly a third of antidepressant drug studies are never published in the medical literature, and nearly all of those happen to show that the drug being tests failed to work.
Only Drugs That are Safe Should be put on the Market. Drug developers are just beginning to come to grips with recent FDA oversight reforms and how they will affect drug safety. But, it appears that industry and consumer advocates are not together on how well the overhaul will be able to prevent future drug safety scandals.

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Review Optivar Safety Reports submitted to FDA

Total Optivar reports: 3.
Optivar FDA safety alerts: No.
   Reported hospitalizations: 3.
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FDA Reported Optivar Side Effects: punctate keratitis, keratoconjunctivitis sicca, depression, caustic injury, visual acuity reduced, dysgeusia.
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Optivar Side Effects Report #5622695-7
Physician from UNITED STATES reported OPTIVAR problem on Feb 08, 2008. Female patient, child 10 years of age, was diagnosed with conjunctivitis allergic and was treated with OPTIVAR. After drug was administered, patient experienced the following problems/side effects: anxiety, ataxia, confusional state, disorientation, flushing, mental impairment, mydriasis, nystagmus. OPTIVAR dosage: unknown. Patient was hospitalized. Patient recovered.

Optivar Side Effects Report #5638060-2
OPTIVAR problem was reported by a Pharmacist from UNITED STATES on Feb 22, 2008. Female patient was diagnosed with hypersensitivity and was treated with OPTIVAR. After drug was administered, patient experienced the following problems/side effects: asthenia, dizziness, hallucination, vision blurred. OPTIVAR dosage: unknown. Patient was hospitalized. Patient recovered.

Optivar Side Effects Report #5455643-3
Health Professional from UNITED STATES reported OPTIVAR problem on Aug 31, 2007. Female patient, 43 years of age, was diagnosed with conjunctivitis allergic and was treated with OPTIVAR. After drug was administered, patient experienced the following problems/side effects: caustic injury, depression, keratoconjunctivitis sicca, punctate keratitis. OPTIVAR dosage: unknown. During the same period patient was treated with TOBRADEX, LOTEMAX, ACULAR, REFRESH TEAR. Patient was hospitalized and became disabled. Patient recovered.


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anxiety, ataxia, confusional state, disorientation, flushing, mental impairment, mydriasis, nystagmus, , was diagnosed with conjunctivitis allergic and was diagnosed with hypersensitivity and was diagnosed with conjunctivitis allergic and