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Meprobamate adverse events reported to FDA.

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Summary

FDA Adverse Reports: 13. View All

Meprobamate FDA safety alerts: No

Reported deaths: 8

Reported hospitalizations: 6

Meprobamate Dosage, Warnings, Usage.

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

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6965272-8 | Dizziness, Nausea
on Aug 18, 2010 Female patient from UNITED STATES , 80 years of age, was diagnosed with anxiety (What is anxiety?), stress (What is stress?) and was treated with Meprobamate (View Usage). Patient experienced the following unwanted or unexpected effects: dizziness (What is dizziness?), nausea (What is nausea?). Meprobamate dosage: 400 Mg, Bid, Oral. During the same period patient was treated with VITAMINS (View Vitamins Review and Vitamins Label ), HIGH BLOOD PRESSURE (BP) (View High Blood Pressure (bp) Review and High Blood Pressure (bp) Label ). Patient was hospitalized.

6946634-1 | Blood Alcohol Increased, Cholestasis, Loss Of Consciousness, Sinus Tachycardia, Ventricular Extrasystoles, Ventricular Fibrillation
Patient was taking Meprobamate (View Usage). Patient had the following side effects: blood alcohol increased, cholestasis, loss of consciousness, sinus tachycardia, ventricular extrasystoles, ventricular fibrillation on Aug 04, 2010 from FRANCE Additional patient health information: Male patient , 35 years of age, . Meprobamate dosage: . During the same period patient was treated with BACLOFEN (View Baclofen Review and Baclofen Label ), ALCOHOL (ALCOHOL) (View Alcohol (alcohol) Review and Alcohol (alcohol) Label ). Patient was hospitalized.

6895377-1 | Drowning, Haemangioma Of Liver, Injury, Mental Impairment
Adverse event was reported on Jul 23, 2010 by a Female patient taking Meprobamate (View Usage) (Dosage: Unk) . Location: UNITED STATES , 32 years of age, After Meprobamate was administered, patient had the following side effects: drowning (What is drowning?), haemangioma of liver, injury, mental impairment. During the same period patient was treated with MORPHINE (Unk) (View Morphine Review and Morphine Label ), COCAINE (Unk) (View Cocaine Review and Cocaine Label ), HYDROCODONE BITARTRATE (Unk) (View Hydrocodone Bitartrate Review and Hydrocodone Bitartrate Label ), ALPRAZOLAM (Unk) (View Alprazolam Review and Alprazolam Label ), SERTRALINE HYDROCHLORIDE (Unk) (View Sertraline Hydrochloride Review and Sertraline Hydrochloride Label ), CARISOPRODOL (Unk) (View Carisoprodol Review and Carisoprodol Label ).

6857349-2 | Drowning, Injury
on Jul 06, 2010 Female patient from UNITED STATES , 32 years of age, was treated with Meprobamate (View Usage). Patient experienced the following unwanted or unexpected effects: drowning (What is drowning?), injury. Meprobamate dosage: Unk. During the same period patient was treated with MORPHINE (Unk) (View Morphine Review and Morphine Label ), COCAINE (Unk) (View Cocaine Review and Cocaine Label ), HYDROCODONE (Unk) (View Hydrocodone Review and Hydrocodone Label ), ALPRAZOLAM (Unk) (View Alprazolam Review and Alprazolam Label ), SERTRALINE HCL (Unk) (View Sertraline Hcl Review and Sertraline Hcl Label ), CARISOPRODOL (Unk) (View Carisoprodol Review and Carisoprodol Label ).


6652097-6 |
on Mar 22, 2010 Male patient from UNITED STATES , 33 years of age, was treated with Meprobamate (View Usage). . Meprobamate dosage: . During the same period patient was treated with OXYCODONE HCL (View Oxycodone Hcl Review and Oxycodone Hcl Label ), HYDROCODONE BITARTRATE AND ACETAMINOPHEN (View Hydrocodone Bitartrate And Acetaminophen Review and Hydrocodone Bitartrate And Acetaminophen Label ), BENZODIAZEPINE DERIVATIVES (View Benzodiazepine Derivatives Review and Benzodiazepine Derivatives Label ).

6621920-3 |
Patient was taking Meprobamate (View Usage). on Feb 16, 2010 from UNITED STATES Additional patient health information: Male patient , 33 years of age, . Meprobamate dosage: Oral. During the same period patient was treated with HYDROCODONE BITARTRATE AND ACETAMINOPHEN (Oral) (View Hydrocodone Bitartrate And Acetaminophen Review and Hydrocodone Bitartrate And Acetaminophen Label ), ALPRAZOLAM (Oral) (View Alprazolam Review and Alprazolam Label ), OXYCODONE HCL (Oral) (View Oxycodone Hcl Review and Oxycodone Hcl Label ).

6223198-1 | Amnesia, Aspiration, Sleep-related Eating Disorder
Adverse event was reported on Jun 01, 2009 by a Female patient taking Meprobamate (View Usage) (Dosage: Unk) was diagnosed with insomnia and. Location: UNITED STATES , 28 years of age, Patient experienced the following unwanted or unexpected effects: amnesia, aspiration, sleep-related eating disorder. During the same period patient was treated with SOMA (Unk) (View Soma Review and Soma Label ), HYDROCODONE BITARTRATE (Unk) (View Hydrocodone Bitartrate Review and Hydrocodone Bitartrate Label ), ACETAMINOPHEN (Unk) (View Acetaminophen Review and Acetaminophen Label ), AMBIEN (Frequently Took 3 To 4 Zolpidem Tablets At A Time) (View Ambien Review and Ambien Label ).

5932194-0 | Neonatal Respiratory Distress Syndrome, Premature Baby, Small For Dates Baby
on Oct 06, 2008 Female patient from HUNGARY , weighting 2.78 lb, was treated with Meprobamate (View Usage). Patient had the following side effects: neonatal respiratory distress syndrome, premature baby, small for dates baby. Meprobamate dosage: Transplacental.

5631490-4 | Cardio-respiratory Arrest
on Feb 04, 2008 Female patient from UNITED STATES , 39 years of age, was treated with Meprobamate (View Usage). After Meprobamate was administered, patient had the following side effects: cardio-respiratory arrest. Meprobamate dosage: . During the same period patient was treated with BUPROPION HYDROCHLORIDE (View Bupropion Hydrochloride Review and Bupropion Hydrochloride Label ), ANTIHISTAMINE/DECONGESTION SRC (View Antihistamine/decongestion Src Review and Antihistamine/decongestion Src Label ), DEXTROMETHORPHAN HYDROBROMIDE (View Dextromethorphan Hydrobromide Review and Dextromethorphan Hydrobromide Label ), DIPHENHYDRAMINE HCL (View Diphenhydramine Hcl Review and Diphenhydramine Hcl Label ).

5326544-6 | Cerebral Haemorrhage, Depressed Level Of Consciousness, Fall
Patient was taking Meprobamate (View Usage). Patient experienced the following unwanted or unexpected effects: cerebral haemorrhage, depressed level of consciousness, fall (What is fall?) on Apr 26, 2007 from UNITED STATES Additional patient health information: Female patient , 71 years of age, weighting 130.0 lb, was diagnosed with back pain (What is back pain?) and. Meprobamate dosage: Oral. Patient was hospitalized.

5239370-3 | Accident, Fall, Hip Fracture, Hip Surgery
Adverse event was reported on Feb 05, 2007 by a Female patient taking Meprobamate (View Usage) (Dosage: ) was diagnosed with osteoporosis (What is osteoporosis?) and. Location: UNITED STATES , 68 years of age, Patient had the following side effects: accident, fall (What is fall?), hip fracture, hip surgery. During the same period patient was treated with MIACALCIN (200 Iu, Qd) (View Miacalcin Review and Miacalcin Label ). Patient was hospitalized.

5188786-2 | Bezoar, Convulsion, Depressed Level Of Consciousness, Hypotension, Intentional Self-injury, Somnolence
on Dec 01, 2006 Male patient from UNITED STATES , 45 years of age, was diagnosed with ill-defined disorder and was treated with Meprobamate (View Usage). After Meprobamate was administered, patient had the following side effects: bezoar, convulsion, depressed level of consciousness, hypotension, intentional self-injury, somnolence. Meprobamate dosage: . During the same period patient was treated with CARBAMAZEPINE (View Carbamazepine Review and Carbamazepine Label ). Patient was hospitalized.

5038816-3 | Agitation, Blood Glucose Increased, Blood Pressure Diastolic Decreased, Blood Urine Present, Cerebral Atrophy, Convulsion, Fall
on Jun 12, 2006 Female patient from UNITED KINGDOM , 80 years of age, was diagnosed with nervousness and was treated with Meprobamate (View Usage). Patient experienced the following unwanted or unexpected effects: agitation, blood glucose increased, blood pressure diastolic decreased, blood urine present, cerebral atrophy, convulsion, fall (What is fall?). Meprobamate dosage: 2 Tablets Tid (400 Mg), Oral 1960's. During the same period patient was treated with AMITRIPTYLLINE (AMITRIPTYLINE) (View Amitriptylline (amitriptyline) Review and Amitriptylline (amitriptyline) 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 Meprobamate 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 Meprobamate quality problem: suspected counterfeit product, potentially contaminated product indicated by suspicious odor or unusual color, inaccurate or unreadable product labeling
3. Potential Meprobamate 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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Meprobamate Reactions
Accident
Agitation
Amnesia
Aspiration
Bezoar
Blood Alcohol Increased
Blood Glucose Increased
Blood Pressure Diastolic Decreased
Blood Urine Present
Cardio-respiratory Arrest
Cerebral Atrophy
Cerebral Haemorrhage
Cholestasis
Convulsion
Death
Depressed Level Of Consciousness
DizzinessWhat is Dizziness?
DrowningWhat is Drowning?
FallWhat is Fall?
Haemangioma Of Liver
Hip Fracture
Hip Surgery
Hypotension
Injury
Intentional Self-injury
Loss Of Consciousness
Mental Impairment
NauseaWhat is Nausea?
Neonatal Respiratory Distress Syndrome
Premature Baby
Meprobamate 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 Meprobamate 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!