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1.5 million people annually are harmed from drug errors.
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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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Community-reported Predte side effects:

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Review Predte Safety Reports submitted to FDA

Total Predte reports: 4.
Predte FDA safety alerts: No.
   Reported hospitalizations: 1.
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FDA Reported Predte Side Effects: seidel test positive, scleral thinning, hypotony of eye, eye penetration, cataract operation complication.
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Predte Side Effects Report #5591242-0
Physician from UNITED STATES reported PREDTE problem on Jan 14, 2008. Female patient, 72 years of age, was diagnosed with postoperative care, diabetes mellitus and was treated with PREDTE. After drug was administered, patient experienced the following problems/side effects: choking, cough, dry throat, dyspnoea, hypersensitivity, throat tightness, wheezing. PREDTE dosage: unknown. During the same period patient was treated with ACULAR, ZYMAR, GLYBURIDE. Patient was hospitalized. Patient recovered.

Predte Side Effects Report #5591894-5
PREDTE problem was reported by a Physician from KOREA, REPUBLIC OF on Jan 08, 2008. Male patient, 26 years of age, was diagnosed with ulcerative keratitis and was treated with PREDTE. After drug was administered, patient experienced the following problems/side effects: conjunctival cyst, foreign body sensation in eyes, photopsia. PREDTE dosage: unknown. During the same period patient was treated with OPTICROM. Patient recovered.

Predte Side Effects Report #5573751-3
Consumer or non-health professional from UNITED STATES reported PREDTE problem on Dec 18, 2007. Female patient was diagnosed with postoperative care, diabetes mellitus and was treated with PREDTE. After drug was administered, patient experienced the following problems/side effects: choking, cough, dry throat, dyspnoea. PREDTE dosage: unknown. During the same period patient was treated with ACULAR, ZYMAR, GLYBURIDE. Patient recovered.

Predte Side Effects Report #5463338-5
PREDTE problem was reported by a Physician from UNITED STATES on Sept 11, 2007. Female patient was diagnosed with postoperative care, intraocular pressure increased, eye inflammation and was treated with PREDTE. After drug was administered, patient experienced the following problems/side effects: cataract operation complication, eye penetration, hypotony of eye, scleral thinning, seidel test positive. PREDTE dosage: unknown. During the same period patient was treated with DICLOFENAC, TIMOPTIC, XALATAN, TOBRAMYCIN. Patient recovered.


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choking, cough, dry throat, dyspnoea, hypersensitivity, throat tightness, wheezing, conjunctival cyst, foreign body sensation in eyes, photopsia, , was diagnosed with postoperative care, diabetes mellitus and was diagnosed with ulcerative keratitis and