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Remergil adverse events reported to FDA.

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Summary

FDA Adverse Reports: 2. View All

Remergil FDA safety alerts: No

Reported hospitalizations: 3

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

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6267961-X | Facial Bones Fracture, Fall, Grand Mal Convulsion, Jaw Fracture, Loss Of Consciousness
on Jun 29, 2009 Female patient from UNITED STATES , 55 years of age, was diagnosed with depression (What is depression?) and was treated with Remergil (View Usage). Patient experienced the following unwanted or unexpected effects: facial bones fracture, fall (What is fall?), grand mal convulsion, jaw fracture, loss of consciousness. Remergil dosage: 30 Mg Daily Oral. During the same period patient was treated with LORAZEPAM (1.5 Mg Daily) (View Lorazepam Review and Lorazepam Label ), ZOPICLON (View Zopiclon Review and Zopiclon Label ).

4596483-7 | Aphasia, Blood Creatine Phosphokinase Increased, Confusional State, Disorientation, Hyponatraemia, Nausea, Thinking Abnormal
Patient was taking Remergil (View Usage). Patient had the following side effects: aphasia (What is aphasia?), blood creatine phosphokinase increased, confusional state, disorientation, hyponatraemia, nausea (What is nausea?), thinking abnormal on Feb 21, 2005 from Additional patient health information: Female patient , 60 years of age, was diagnosed with depression (What is depression?), epilepsy (What is epilepsy?) and. Remergil dosage: 15 Mg. During the same period patient was treated with RISPERDAL (1 Mg) (View Risperdal Review and Risperdal Label ), CARBAMAZEPINE (1000 Mg) (View Carbamazepine Review and Carbamazepine Label ), STILNOX (10 Mg) (View Stilnox Review and Stilnox 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 Remergil 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 Remergil quality problem: suspected counterfeit product, potentially contaminated product indicated by suspicious odor or unusual color, inaccurate or unreadable product labeling
3. Potential Remergil 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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During the same period patient was treated with DIPIPERON (40 Mg Daily), REMERGIL (30 Mg Daily), ALLOPURINOL (100 Mg Daily), CARVEDILOL (25 Mg Daily), MOXONIDINE (0.3 Mg Daily ...<<<<

... Paspertin Review and Paspertin Label ), PANTOPRAZOLE SODIUM (View Pantoprazole Sodium Review and Pantoprazole Sodium Label ), REMERGIL (View Remergil Review and Remergil Label ...<<<<

)During the same period patient was treated with REMERGIL (View Remergil Review and Remergil Label ), VENLAFAXINE HCL (View Venlafaxine Hcl Review and Venlafaxine Hcl Label ...<<<<

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Remergil Reactions
AphasiaWhat is Aphasia?
Blood Creatine Phosphokinase Increased
Confusional State
Disorientation
Facial Bones Fracture
FallWhat is Fall?
Grand Mal Convulsion
Hyponatraemia
Jaw Fracture
Loss Of Consciousness
NauseaWhat is Nausea?
Thinking Abnormal
Remergil Side Effects Notice - The material on this site is for informational purposes only, and is not a substitute for medical advice, diagnosis or treatment provided by a qualified health care provider. PatientsVille.com does not provide medical advice, diagnosis or treatment. The information regarding Remergil adverse reports, reviews and polls contained on PatientsVille.com site has not been scientifically or otherwise verified as to a cause and effect relationship and cannot be used to estimate the incidence of adverse drug reactions or for establishing or changing of patient treatments. Thank you for visiting Patientsville.com!