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Niravam adverse events reported to FDA.

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Summary

FDA Adverse Reports: 5. View All

Niravam FDA safety alerts: No

Reported hospitalizations: 5

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

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5732591-2 | Leg Amputation, Myocardial Infarction
on Apr 19, 2008 Female patient from UNITED STATES , 42 years of age, was diagnosed with panic attack and was treated with Niravam (View Usage). Patient experienced the following unwanted or unexpected effects: leg amputation, myocardial infarction. Niravam dosage: 1mg. During the same period patient was treated with AMLODIPINE (View Amlodipine Review and Amlodipine Label ), SERTRALINE (View Sertraline Review and Sertraline Label ), FLEXERIL (View Flexeril Review and Flexeril Label ), LORTAB (View Lortab Review and Lortab Label ), VALIUM (View Valium Review and Valium Label ), ATIVAN (View Ativan Review and Ativan Label ), CRESTOR (View Crestor Review and Crestor Label ), TRICOR (View Tricor Review and Tricor Label ). Patient was hospitalized.

5177132-6 | Neuroleptic Malignant Syndrome
Patient was taking Niravam (View Usage). Patient had the following side effects: neuroleptic malignant syndrome on Nov 29, 2006 from UNITED STATES Additional patient health information: Male patient , 74 years of age, was diagnosed with major depression and. Niravam dosage: . During the same period patient was treated with PAROXETINE HCL (View Paroxetine Hcl Review and Paroxetine Hcl Label ). Patient was hospitalized.

5102059-5 | Overdose
Adverse event was reported on Aug 31, 2006 by a Male patient taking Niravam (View Usage) (Dosage: 30 In 1 D, Oral) . Location: UNITED STATES , 40 years of age, After Niravam was administered, patient had the following side effects: overdose. Patient was hospitalized.

5102054-6 | Overdose
on Aug 31, 2006 Female patient from UNITED STATES , 68 years of age, was treated with Niravam (View Usage). Patient experienced the following unwanted or unexpected effects: overdose. Niravam dosage: 6 In 1 H, Oral. Patient was hospitalized.


4982854-3 | Chest Discomfort, Chest Pain, Dyspnoea, Erythema, Heart Rate Increased, Hepatic Enzyme Increased, Nausea, Rash
on Apr 12, 2006 Female patient from UNITED STATES , 34 years of age, weighting 285.0 lb, was diagnosed with anxiety (What is anxiety?) and was treated with Niravam (View Usage). Patient had the following side effects: chest discomfort, chest pain (What is chest pain?), dyspnoea, erythema, heart rate increased, hepatic enzyme increased, nausea (What is nausea?), rash (What is rash?). Niravam dosage: 1 Once Oral. 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 Niravam 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 Niravam quality problem: suspected counterfeit product, potentially contaminated product indicated by suspicious odor or unusual color, inaccurate or unreadable product labeling
3. Potential Niravam 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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Niravam Reactions
Chest Discomfort
Chest PainWhat is Chest pain?
Dyspnoea
Erythema
Heart Rate Increased
Hepatic Enzyme Increased
Leg Amputation
Myocardial Infarction
NauseaWhat is Nausea?
Neuroleptic Malignant Syndrome
Overdose
RashWhat is Rash?
Niravam 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 Niravam 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!