Brinerdin Side Effects

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Brinerdin adverse events reported to FDA.

Have You Experienced unusual Brinerdin symptoms? PatientsVille.com collects and analyzes Brinerdin side effect and adverse reports submitted by Brinerdin users, such as .

Summary

FDA Adverse Reports: 3. View All

Brinerdin FDA safety alerts: No

Reported hospitalizations: 3

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Often additional risks of using a medication, such as Brinerdin, 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 Brinerdin users, Learn more about unwanted side effects & find ways to reduce them. Browse Brinerdin Adverse Reports reported to FDA and participate in Brinerdin discussion, find alternative treatments and find ways to avoid or reduce risks associated with using Brinerdin. 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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Brinerdin Adverse Effect Reports (FDA)

4702218-7 | Gastrointestinal Ulcer Perforation
on Jun 20, 2005 Female patient from , 73 years of age, was diagnosed with hypertension and was treated with Brinerdin (View Usage). Patient experienced the following unwanted or unexpected effects: gastrointestinal ulcer perforation. Brinerdin dosage: 1 Df, Qd. During the same period patient was treated with ANTIINFLAMMATORY/ANTIRHEUMATIC NON STEROIDS (Occasionally) (View Antiinflammatory/antirheumatic Non-steroids Review and Antiinflammatory/antirheumatic Non-steroids Label ). Patient was hospitalized.

4702217-5 | Gastrointestinal Ulcer Perforation, Helicobacter Infection, Peptic Ulcer Perforation
Patient was taking Brinerdin (View Usage). Patient had the following side effects: gastrointestinal ulcer perforation, helicobacter infection, peptic ulcer perforation on Jun 20, 2005 from Additional patient health information: Female patient , 73 years of age, was diagnosed with hypertension, spinal osteoarthritis and. Brinerdin dosage: 1 Df, Qd. During the same period patient was treated with ANTIINFLAMMATORY/ANTIRHEUMATIC NON STEROIDS (Occasionally) (View Antiinflammatory/antirheumatic Non-steroids Review and Antiinflammatory/antirheumatic Non-steroids Label ). Patient was hospitalized.

4555662-5 | Contusion, Electrocardiogram Qt Prolonged, Face Injury, Feeling Abnormal, Hypokalaemia, Syncope
Adverse event was reported on Jan 05, 2005 by a Female patient taking Brinerdin (View Usage) (Dosage: 1 Tablet/day) was diagnosed with hypertension, depression (What is depression?) and. Location: , 62 years of age, After Brinerdin was administered, patient had the following side effects: contusion, electrocardiogram qt prolonged, face injury, feeling abnormal, hypokalaemia, syncope. During the same period patient was treated with FLUOXETINE HCL (40 Mg/day) (View Fluoxetine Hcl Review and Fluoxetine Hcl Label ), LITHIUM CARBONATE (1.5 Tablet/day) (View Lithium Carbonate Review and Lithium Carbonate Label ), BUSPAR (20 Mg/day) (View Buspar Review and Buspar Label ). Patient was hospitalized.

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Brinerdin Questions, Answers, Feedback and Comments

Comments to date: 2. Page 1 of 1.

peter jamaica	10:45am on Tuesday, April 19th, 2011
What'swhat are the side effects of brinerdin? on Your Mind?
Dr.Valentine Enugu	1:30pm on Tuesday, December 7th, 2010
Has Brinerdin been implicated by any current scientific research in the aetiology of Erectal dysfunc... read more »

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 Brinerdin 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 Brinerdin quality problem: suspected counterfeit product, potentially contaminated product indicated by suspicious odor or unusual color, inaccurate or unreadable product labeling
3. Potential Brinerdin 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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	Yes, Moderate
	Yes, Minor
	No

	Exceeded Expectations
	Effective
	Somewhat Effective
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Brinerdin adverse events reported to FDA.

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Brinerdin Adverse Effect Reports (FDA)

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Brinerdin Reactions

Contusion
Electrocardiogram Qt Prolonged
Face Injury
Feeling Abnormal
Gastrointestinal Ulcer Perforation
Helicobacter Infection
Hypokalaemia
Peptic Ulcer Perforation
Syncope

BRINERDIN Side Effects

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Brinerdin adverse events reported to FDA.

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Brinerdin Adverse Effect Reports (FDA)

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Brinerdin Reactions