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Efexor adverse events reported to FDA.

Have You Experienced unusual Efexor symptoms? PatientsVille.com collects and analyzes Efexor side effect and adverse reports submitted by Efexor users, such as sleeplessness, sleepy, fatigue, headaches |.

Summary

FDA Adverse Reports: 3. View All

Efexor FDA safety alerts: No

Reported deaths: 1

Reported hospitalizations: 2

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1Tinnitus
2Brief Yawning Episodes
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Often additional risks of using a medication, such as Efexor, 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 Efexor users, Learn more about unwanted side effects & find ways to reduce them. Browse Efexor Adverse Reports reported to FDA and participate in Efexor discussion, find alternative treatments and find ways to avoid or reduce risks associated with using Efexor. 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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Efexor Adverse Effect Reports (FDA)

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5011121-7 | Decreased Appetite, Diarrhoea, Dizziness, Histrionic Personality Disorder, Judgement Impaired, Loss Of Libido, Motion Sickness, Nausea
on May 12, 2006 Female patient from UNITED KINGDOM , 41 years of age, was treated with Efexor (View Usage). Patient experienced the following unwanted or unexpected effects: decreased appetite, diarrhoea, dizziness (What is dizziness?), histrionic personality disorder, judgement impaired, loss of libido, motion sickness (What is motion sickness?), nausea (What is nausea?). Efexor dosage: 75 Mg.

4893524-4 | Blood Bicarbonate Decreased, Blood Calcium Decreased, Blood Creatine Increased, Blood Magnesium Decreased, Circulatory Collapse, Convulsion, Dyspnoea, Hypokalaemia, Hyponatraemia
Patient was taking Efexor (View Usage). Patient had the following side effects: blood bicarbonate decreased, blood calcium decreased, blood creatine increased, blood magnesium decreased, circulatory collapse, convulsion, dyspnoea, hypokalaemia, hyponatraemia on Jan 11, 2006 from AUSTRALIA Additional patient health information: Male patient , 60 years of age, . Efexor dosage: 225 Mg 1x Per 1 Day. During the same period patient was treated with OLANZAPINE (View Olanzapine Review and Olanzapine Label ), MIRTAZAPINE (View Mirtazapine Review and Mirtazapine Label ), DIAZEPAM (View Diazepam Review and Diazepam Label ), CHLORPROMAZINE (50 Mg, As Necessary; 100 Mg In The Morning, And Took An Additional 100 Mg) (View Chlorpromazine Review and Chlorpromazine Label ), ZOLPIDEM TARTRATE (View Zolpidem Tartrate Review and Zolpidem Tartrate Label ). Patient was hospitalized.

4736462-X | Alanine Aminotransferase Increased, Aspartate Aminotransferase Increased, Blood Alkaline Phosphatase Increased, Bone Pain, Condition Aggravated, Creatinine Renal Clearance Increased, Diarrhoea
Adverse event was reported on Jul 20, 2005 by a Female patient taking Efexor (View Usage) (Dosage: See Image) was diagnosed with personality disorder (What is personality disorder?) and. Location: SWITZERLAND , 77 years of age, After Efexor was administered, patient had the following side effects: alanine aminotransferase increased, aspartate aminotransferase increased, blood alkaline phosphatase increased, bone pain, condition aggravated, creatinine renal clearance increased, diarrhoea. During the same period patient was treated with TRILEPTAL (See Image) (View Trileptal Review and Trileptal Label ). Patient was hospitalized.


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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 Efexor 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 Efexor quality problem: suspected counterfeit product, potentially contaminated product indicated by suspicious odor or unusual color, inaccurate or unreadable product labeling
3. Potential Efexor 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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