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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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Review Visken Safety Reports submitted to FDA

Total Visken reports: 9.
Visken FDA safety alerts: No.
   Reported hospitalizations: 7.
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FDA Reported Visken Side Effects: hypertension, systemic lupus erythematosus, benign hydatidiform mole, abortion spontaneous, lacrimation increased, heart rate increased, eyelid oedema, electrocardiogram qt prolonged, dyspnoea, dysphonia, anaphylactic shock.
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Visken Side Effects Report #5226961-9
Consumer or non-health professional from FRANCE reported VISKEN problem on Jan 22, 2007. Female patient, 26 years of age, was diagnosed with arrhythmia supraventricular and was treated with VISKEN. After drug was administered, patient experienced the following problems/side effects: abortion spontaneous, benign hydatidiform mole, systemic lupus erythematosus. VISKEN dosage: unknown. Patient was hospitalized. Patient recovered.

Visken Side Effects Report #5312140-3
VISKEN problem was reported by a Consumer or non-health professional from FRANCE on Apr 18, 2007. Female patient, 26 years of age, was diagnosed with arrhythmia supraventricular and was treated with VISKEN. After drug was administered, patient experienced the following problems/side effects: abortion spontaneous, benign hydatidiform mole, systemic lupus erythematosus. VISKEN dosage: unknown. Patient was hospitalized. Patient recovered.

Visken Side Effects Report #5312710-2
Consumer or non-health professional from FRANCE reported VISKEN problem on Apr 18, 2007. Female patient, 26 years of age, was diagnosed with arrhythmia supraventricular and was treated with VISKEN. After drug was administered, patient experienced the following problems/side effects: abortion spontaneous, benign hydatidiform mole, systemic lupus erythematosus. VISKEN dosage: unknown. Patient was hospitalized. Patient recovered.

Visken Side Effects Report #5364682-2
VISKEN problem was reported by a Health Professional from POLAND on June 11, 2007. Female patient was treated with VISKEN. After drug was administered, patient experienced the following problems/side effects: bradycardia. VISKEN dosage: 5 MG/DAY. During the same period patient was treated with BETALOC ZOK, KALIPOZ, SIMVASTATIN, ACARD, GLUCOSAMINE, CHONDROITIN A. Patient was hospitalized. Patient recovered.

Visken Side Effects Report #5373247-8
Consumer or non-health professional from BRAZIL reported VISKEN problem on June 15, 2007. Female patient, 27 years of age, weighting 229.3 lb, was diagnosed with hypertension and was treated with VISKEN. After drug was administered, patient experienced the following problems/side effects: blood pressure increased, insomnia, malaise, suffocation feeling, tachycardia, throat tightness, tremor. VISKEN dosage: 10 MG, ONCE/SINGLE. During the same period patient was treated with VITAMIN. Patient recovered.

Visken Side Effects Report #5081317-7
VISKEN problem was reported by a Health Professional from BRAZIL on Aug 03, 2006. Male patient, 46 years of age, weighting 154.3 lb, was diagnosed with hypertrophic cardiomyopathy and was treated with VISKEN. After drug was administered, patient experienced the following problems/side effects: hypotonia, muscle atrophy, muscular weakness, tendonitis, tremor. VISKEN dosage: unknown. Patient recovered.

Visken Side Effects Report #5401181-3
Consumer or non-health professional from FRANCE reported VISKEN problem on July 24, 2007. Male patient, 76 years of age, was diagnosed with hypertension, sinusitis and was treated with VISKEN. After drug was administered, patient experienced the following problems/side effects: anaphylactic shock, dysphonia, dyspnoea, electrocardiogram qt prolonged, erythema, eyelid oedema, heart rate increased, hypertension, lacrimation increased. VISKEN dosage: unknown. During the same period patient was treated with TAVANIC. Patient was hospitalized. Patient recovered.

Visken Side Effects Report #5447174-1
VISKEN problem was reported by a Consumer or non-health professional from FRANCE on Sept 05, 2007. Male patient, 76 years of age, was diagnosed with hypertension, sinusitis and was treated with VISKEN. After drug was administered, patient experienced the following problems/side effects: anaphylactic shock, dysphonia, dyspnoea, electrocardiogram qt prolonged, erythema, eyelid oedema, heart rate increased, hypertension, lacrimation increased. VISKEN dosage: unknown. During the same period patient was treated with TAVANIC. Patient was hospitalized. Patient recovered.

Visken Side Effects Report #5450866-1
Consumer or non-health professional from BRAZIL reported VISKEN problem on Sept 05, 2007. Female patient, 42 years of age, weighting 280.0 lb, was diagnosed with hypertension, hyperthyroidism and was treated with VISKEN. After drug was administered, patient experienced the following problems/side effects: eclampsia, feeling cold, hypertension. VISKEN dosage: 10 MG, Q12H. During the same period patient was treated with PURAN T. Patient was hospitalized. Patient recovered.


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abortion spontaneous, benign hydatidiform mole, systemic lupus erythematosus abortion spontaneous, benign hydatidiform mole, systemic lupus erythematosus, was diagnosed with arrhythmia supraventricular and was diagnosed with arrhythmia supraventricular and