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Prazosin adverse events reported to FDA.

Have You Experienced unusual Prazosin symptoms? PatientsVille.com collects and analyzes Prazosin side effect and adverse reports submitted by Prazosin users, such as fatigue, nausea, short breath. purging |.

Summary

FDA Adverse Reports: 4. View All

Prazosin FDA safety alerts: No

Reported deaths: 2

Reported hospitalizations: 11

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Recent Drug Reports

fatigue, nausea, short breath. purging

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Often additional risks of using a medication, such as Prazosin, become known after product is used by a larger number of patients, for a longer period of time, and by patients with different health characteristics from those studied before drug approval. This page allows You to Find answers and discuss health symptoms with other Prazosin users, Learn more about unwanted side effects & find ways to reduce them. Browse Prazosin Adverse Reports reported to FDA and participate in Prazosin discussion, find alternative treatments and find ways to avoid or reduce risks associated with using Prazosin. You can also Post a question to users community or Ask a Doctor. PatientsVille.com is Your Complete Guide to all common, undocumented and undisclosed side effects associated with drugs and vaccines. Browse More Drug Reports Here: A  B  C  D  E  F  G  H  I  J  K  L  M  N  O  P  Q  R  S  T  U  V  W  X  Y  Z

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Prazosin Adverse Effect Reports (FDA)

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6596492-2 | Fall, Head Injury, Hypotension, Loss Of Consciousness, Syncope, Unevaluable Event
on Feb 22, 2010 Male patient from UNITED STATES , 62 years of age, weighting 292.3 lb, was diagnosed with post-traumatic stress disorder (What is post-traumatic stress disorder?) and was treated with Prazosin (View Usage). Patient experienced the following unwanted or unexpected effects: fall (What is fall?), head injury, hypotension, loss of consciousness, syncope, unevaluable event. Prazosin dosage: 5 Mg Every Day Po. Patient was hospitalized.

4917075-3 | Dizziness
Patient was taking Prazosin (View Usage). Patient had the following side effects: dizziness (What is dizziness?) on Feb 16, 2006 from UNITED STATES Additional patient health information: Male patient , 59 years of age, weighting 218.0 lb, . Prazosin dosage: . During the same period patient was treated with SILDENAFIL CITRATE (View Sildenafil Citrate Review and Sildenafil Citrate Label ), CHLORPHENIRAMINE MALEATE (View Chlorpheniramine Maleate Review and Chlorpheniramine Maleate Label ), OMEPRAZOLE (View Omeprazole Review and Omeprazole Label ), FLUNISOLIDE (View Flunisolide Review and Flunisolide Label ).

4778450-3 | Dizziness
Adverse event was reported on Sep 23, 2005 by a Male patient taking Prazosin (View Usage) (Dosage: ) . Location: UNITED STATES , 80 years of age, weighting 177.9 lb, After Prazosin was administered, patient had the following side effects: dizziness (What is dizziness?). During the same period patient was treated with COUMADIN (View Coumadin Review and Coumadin Label ), FLUOCINOLONE ACETONIDE (View Fluocinolone Acetonide Review and Fluocinolone Acetonide Label ), FLUOCINONIDE (View Fluocinonide Review and Fluocinonide Label ), MECLIZINE HCL (View Meclizine Hcl Review and Meclizine Hcl Label ), SULFAMETHOXAZOLE + TRIMETHOPRIM (View Sulfamethoxazole + Trimethoprim Review and Sulfamethoxazole + Trimethoprim Label ), ISOSORBIDE DINITRATE (View Isosorbide Dinitrate Review and Isosorbide Dinitrate Label ), NITROGLYCERIN (View Nitroglycerin Review and Nitroglycerin Label ), ASPIRIN (View Aspirin Review and Aspirin Label ).

4672452-3 | Depression, Suicidal Ideation
on May 17, 2005 Male patient from , 70 years of age, was diagnosed with prostatism and was treated with Prazosin (View Usage). Patient experienced the following unwanted or unexpected effects: depression (What is depression?), suicidal ideation. Prazosin dosage: 500 Mcg Oral.


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To find out about documented side effects or safety concerns read either the drug label or the drug's package insert. You may also want to speak with your pharmacist or healthcare provider. All medicines have benefits and risks. The risks are the chances that something unwanted or unexpected could happen to you when you use them. You can protect yourself by searching summaries of recent safety alerts, adverse reports. Sometimes there are risks that only come to light after a medical product gets on the market and is used in a larger number of patients, for a longer period of time, and in patients whose health characteristics are different from those of the patients studied before approval.

Be aware of the following potential Prazosin risks to be aware of: 1. Watch for any Serious adverse events, such as life-threatening situation, which can require an admission to hospital or longer-than-expected hospital stay, permanent disability, birth defect, miscarriage, stillbirth, or birth with serious disease requires medical care to prevent permanent damage
2. Any potential Prazosin quality problem: suspected counterfeit product, potentially contaminated product indicated by suspicious odor or unusual color, inaccurate or unreadable product labeling
3. Potential Prazosin use error: mixing up products with similar drug names or packaging, taking wrong dose of a drug because of confusing dosing instructions on label
4. When applicable, Problems with different manufacturer of same medicine: not getting same results from a generic drug as a brand name drug, or from another generic

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