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Mepronizine adverse events reported to FDA.

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Summary

FDA Adverse Reports: 8. View All

Mepronizine FDA safety alerts: No

Reported deaths: 2

Reported hospitalizations: 5

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

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6583637-3 | Coma, Hypokalaemia, Pyrexia
on Feb 01, 2010 Female patient from FRANCE , 63 years of age, was treated with Mepronizine (View Usage). Patient experienced the following unwanted or unexpected effects: coma, hypokalaemia, pyrexia. Mepronizine dosage: . During the same period patient was treated with STILNOX (View Stilnox Review and Stilnox Label ), LEXOMIL (View Lexomil Review and Lexomil Label ), NORSET (View Norset Review and Norset Label ).

5707959-0 | Condition Aggravated, Leukocytosis, Neutrophilia
Patient was taking Mepronizine (View Usage). Patient had the following side effects: condition aggravated, leukocytosis, neutrophilia on Apr 11, 2008 from FRANCE Additional patient health information: Male patient , 38 years of age, . Mepronizine dosage: . During the same period patient was treated with TRANXENE (View Tranxene Review and Tranxene Label ), STILNOX (View Stilnox Review and Stilnox Label ), LEPONEX (From 50 To 400 Mg/day) (View Leponex Review and Leponex Label ). Patient was hospitalized.

5648499-7 | Condition Aggravated, Leukocytosis, Myeloproliferative Disorder, Neutrophilia
Adverse event was reported on Feb 25, 2008 by a Male patient taking Mepronizine (View Usage) (Dosage: ) . Location: FRANCE , 38 years of age, After Mepronizine was administered, patient had the following side effects: condition aggravated, leukocytosis, myeloproliferative disorder, neutrophilia. During the same period patient was treated with TRANXENE (View Tranxene Review and Tranxene Label ), STILNOX (View Stilnox Review and Stilnox Label ), LEPONEX (From 50 To 400 Mg/day) (View Leponex Review and Leponex Label ). Patient was hospitalized.

4876008-9 | Acute Respiratory Failure, Bronchitis, Fall, Hypotension, Inflammation, Leukocytosis, Malaise, Right Ventricular Failure
on Dec 28, 2005 Female patient from FRANCE , 81 years of age, weighting 132.3 lb, was treated with Mepronizine (View Usage). Patient experienced the following unwanted or unexpected effects: acute respiratory failure, bronchitis (What is bronchitis?), fall (What is fall?), hypotension, inflammation, leukocytosis, malaise, right ventricular failure. Mepronizine dosage: . During the same period patient was treated with ZOLPIDEM TARTRATE (View Zolpidem Tartrate Review and Zolpidem Tartrate Label ), XANAX (View Xanax Review and Xanax Label ), ALDACTONE (View Aldactone Review and Aldactone Label ), PREVISCAN (Unk) (View Previscan Review and Previscan Label ), AMLOR (View Amlor Review and Amlor Label ), LASILIX (View Lasilix Review and Lasilix Label ), DISCOTRINE (View Discotrine Review and Discotrine Label ). Patient was hospitalized.


4695866-4 | Dyskinesia, Dysstasia, Fall, Headache, Hyperhidrosis, Hypertension, Insomnia, Muscle Rigidity
on Jun 09, 2005 Female patient from , 60 years of age, was diagnosed with depression (What is depression?) and was treated with Mepronizine (View Usage). Patient had the following side effects: dyskinesia, dysstasia, fall (What is fall?), headache (What is headache?), hyperhidrosis, hypertension, insomnia, muscle rigidity. Mepronizine dosage: . During the same period patient was treated with STILNOX (View Stilnox Review and Stilnox Label ), ANAFRANIL (View Anafranil Review and Anafranil Label ), RISPERDAL (View Risperdal Review and Risperdal Label ), TEMESTA (Unk) (View Temesta Review and Temesta Label ), PROPOFOL (Unk) (View Propofol Review and Propofol Label ). Patient was hospitalized.

4666561-2 | Hyperkalaemia, Hyponatraemia, Inappropriate Antidiuretic Hormone Secretion, Pneumonia
Patient was taking Mepronizine (View Usage). After Mepronizine was administered, patient had the following side effects: hyperkalaemia, hyponatraemia, inappropriate antidiuretic hormone secretion, pneumonia (What is pneumonia?) on Nov 25, 2004 from Additional patient health information: Male patient , 32 years of age, weighting 249.1 lb, . Mepronizine dosage: . During the same period patient was treated with MODECATE (Unk) (View Modecate Review and Modecate Label ), VICTAN (View Victan Review and Victan Label ), STILNOX (Unk) (View Stilnox Review and Stilnox Label ), DEPAKENE (View Depakene Review and Depakene Label ), ISOPTIN (Unk) (View Isoptin Review and Isoptin Label ), ALLOPURINOL (Unk) (View Allopurinol Review and Allopurinol Label ). Patient was hospitalized.

4557173-X | Fluid Replacement, Renal Failure Acute
Adverse event was reported on Jan 11, 2005 by a Female patient taking Mepronizine (View Usage) (Dosage: 1 Df, Qd) was diagnosed with metastases to bone and. Location: , 55 years of age, Patient experienced the following unwanted or unexpected effects: fluid replacement, renal failure acute. During the same period patient was treated with SOPHIDONE (8 Mg, Qd) (View Sophidone Review and Sophidone Label ), EQUANIL (250 Mg, Qd) (View Equanil Review and Equanil Label ), LASILIX (60 Mg, Qd) (View Lasilix Review and Lasilix Label ), SOLU MEDROL (120 Mg, Tid) (View Solu-medrol Review and Solu-medrol Label ), AREDIA (90 Mg, Qmo) (View Aredia Review and Aredia Label ).

4554330-3 | Fluid Replacement, Renal Failure Acute
on Jan 11, 2005 Female patient from , 55 years of age, was diagnosed with metastases to bone and was treated with Mepronizine (View Usage). Patient had the following side effects: fluid replacement, renal failure acute. Mepronizine dosage: 1 Df, Qd. During the same period patient was treated with SOPHIDONE (8 Mg, Qd) (View Sophidone Review and Sophidone Label ), EQUANIL (250 Mg, Qd) (View Equanil Review and Equanil Label ), LASILIX (60 Mg, Qd) (View Lasilix Review and Lasilix Label ), SOLU MEDROL (120 Mg, Tid) (View Solu-medrol Review and Solu-medrol Label ), AREDIA (90 Mg, Qmo) (View Aredia Review and Aredia Label ).


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Mepronizine Questions, Answers, Feedback and Comments

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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 Mepronizine 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 Mepronizine quality problem: suspected counterfeit product, potentially contaminated product indicated by suspicious odor or unusual color, inaccurate or unreadable product labeling
3. Potential Mepronizine 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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Mepronizine Reactions
Acute Respiratory Failure
BronchitisWhat is Bronchitis?
Coma
Condition Aggravated
Dyskinesia
Dysstasia
FallWhat is Fall?
Fluid Replacement
HeadacheWhat is Headache?
Hyperhidrosis
Hyperkalaemia
Hypertension
Hypokalaemia
Hyponatraemia
Hypotension
Inappropriate Antidiuretic Hormone Secretion
Inflammation
Insomnia
Leukocytosis
Malaise
Muscle Rigidity
Myeloproliferative Disorder
Neutrophilia
PneumoniaWhat is Pneumonia?
Pyrexia
Renal Failure Acute
Right Ventricular Failure
Mepronizine 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 Mepronizine 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!