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Tofisopam adverse events reported to FDA.

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Summary

FDA Adverse Reports: 5. View All

Tofisopam FDA safety alerts: No

Reported deaths: 5

Reported hospitalizations: 5

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

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5283030-X | Alanine Aminotransferase Increased, Aspartate Aminotransferase Increased, Bacteraemia, Bacterial Infection, Blood Alkaline Phosphatase Increased, Blood Bilirubin Increased, Blood Bilirubin Unconjugated Increased, Blood Creatinine Increased, Blood Pressure Decreased
on Mar 27, 2007 Male patient from JAPAN , 81 years of age, was diagnosed with seborrhoeic dermatitis, atrial fibrillation (What is atrial fibrillation?), constipation (What is constipation?), nail tinea, cerebral infarction and was treated with Tofisopam (View Usage). Patient experienced the following unwanted or unexpected effects: alanine aminotransferase increased, aspartate aminotransferase increased, bacteraemia, bacterial infection (What is bacterial infection?), blood alkaline phosphatase increased, blood bilirubin increased, blood bilirubin unconjugated increased, blood creatinine increased, blood pressure decreased. Tofisopam dosage: 150 Mg/d. During the same period patient was treated with HIBON (60 Mg/d) (View Hibon Review and Hibon Label ), FUJISMIN (90 Mg/d) (View Fujismin Review and Fujismin Label ), NITOROL (15 Mg/d) (View Nitorol Review and Nitorol Label ), MAGNESIUM OXIDE (2 G/d) (View Magnesium Oxide Review and Magnesium Oxide Label ), CLARITHROMYCIN (200 Mg/d) (View Clarithromycin Review and Clarithromycin Label ), EPINASTINE HYDROCHLORIDE (20 Mg/d) (View Epinastine Hydrochloride Review and Epinastine Hydrochloride Label ), LAMISIL (125 Mg/d) (View Lamisil Review and Lamisil Label ), WARFARIN POTASSIUM (2.5 Mg/d) (View Warfarin Potassium Review and Warfarin Potassium Label ). Patient was hospitalized.

5258521-8 | Alanine Aminotransferase Increased, Aspartate Aminotransferase Increased, Bacteraemia, Bacterial Infection, Blood Alkaline Phosphatase Increased, Blood Bilirubin Increased, Blood Bilirubin Unconjugated Increased, Blood Creatinine Increased, Blood Pressure Decreased
Patient was taking Tofisopam (View Usage). Patient had the following side effects: alanine aminotransferase increased, aspartate aminotransferase increased, bacteraemia, bacterial infection (What is bacterial infection?), blood alkaline phosphatase increased, blood bilirubin increased, blood bilirubin unconjugated increased, blood creatinine increased, blood pressure decreased on Mar 05, 2007 from JAPAN Additional patient health information: Male patient , 81 years of age, was diagnosed with seborrhoeic dermatitis, atrial fibrillation (What is atrial fibrillation?), constipation (What is constipation?), nail tinea, cerebral infarction and. Tofisopam dosage: 150 Mg/d. During the same period patient was treated with HIBON (60 Mg/d) (View Hibon Review and Hibon Label ), FUJISMIN (90 Mg/d) (View Fujismin Review and Fujismin Label ), NITOROL (15 Mg/d) (View Nitorol Review and Nitorol Label ), MAGNESIUM OXIDE (2 G/d) (View Magnesium Oxide Review and Magnesium Oxide Label ), CLARITHROMYCIN (200 Mg/d) (View Clarithromycin Review and Clarithromycin Label ), EPINASTINE HYDROCHLORIDE (20 Mg/d) (View Epinastine Hydrochloride Review and Epinastine Hydrochloride Label ), LAMISIL (125 Mg/d) (View Lamisil Review and Lamisil Label ), WARFARIN POTASSIUM (2.5 Mg/d) (View Warfarin Potassium Review and Warfarin Potassium Label ). Patient was hospitalized.

5255132-5 | Alanine Aminotransferase Increased, Aspartate Aminotransferase Increased, Bacteraemia, Bacterial Infection, Blood Alkaline Phosphatase Increased, Blood Bilirubin Increased, Blood Bilirubin Unconjugated Increased, Blood Creatinine Increased, Blood Pressure Decreased
Adverse event was reported on Feb 27, 2007 by a Male patient taking Tofisopam (View Usage) (Dosage: 150 Mg/d) was diagnosed with seborrhoeic dermatitis, atrial fibrillation (What is atrial fibrillation?), constipation (What is constipation?), nail tinea, cerebral infarction and. Location: JAPAN , 81 years of age, After Tofisopam was administered, patient had the following side effects: alanine aminotransferase increased, aspartate aminotransferase increased, bacteraemia, bacterial infection (What is bacterial infection?), blood alkaline phosphatase increased, blood bilirubin increased, blood bilirubin unconjugated increased, blood creatinine increased, blood pressure decreased. During the same period patient was treated with HIBON (60 Mg/d) (View Hibon Review and Hibon Label ), FUJISMIN (90 Mg/d) (View Fujismin Review and Fujismin Label ), NITOROL (15 Mg/d) (View Nitorol Review and Nitorol Label ), MAGNESIUM OXIDE (2 G/d) (View Magnesium Oxide Review and Magnesium Oxide Label ), CLARITHROMYCIN (200 Mg/d) (View Clarithromycin Review and Clarithromycin Label ), EPINASTINE HYDROCHLORIDE (20 Mg/d) (View Epinastine Hydrochloride Review and Epinastine Hydrochloride Label ), LAMISIL (125 Mg/d) (View Lamisil Review and Lamisil Label ), WARFARIN POTASSIUM (2.5 Mg/d) (View Warfarin Potassium Review and Warfarin Potassium Label ). Patient was hospitalized.

5239371-5 | Alanine Aminotransferase Increased, Aspartate Aminotransferase Increased, Bacteraemia, Bacterial Infection, Blood Alkaline Phosphatase Increased, Blood Bilirubin Increased, Blood Bilirubin Unconjugated Increased, Blood Creatinine Increased, Blood Pressure Decreased
on Feb 13, 2007 Male patient from JAPAN , 81 years of age, was diagnosed with seborrhoeic dermatitis, atrial fibrillation (What is atrial fibrillation?), constipation (What is constipation?), nail tinea, cerebral infarction and was treated with Tofisopam (View Usage). Patient experienced the following unwanted or unexpected effects: alanine aminotransferase increased, aspartate aminotransferase increased, bacteraemia, bacterial infection (What is bacterial infection?), blood alkaline phosphatase increased, blood bilirubin increased, blood bilirubin unconjugated increased, blood creatinine increased, blood pressure decreased. Tofisopam dosage: 150 Mg/d. During the same period patient was treated with HIBON (60 Mg/d) (View Hibon Review and Hibon Label ), FUJISMIN (90 Mg/d) (View Fujismin Review and Fujismin Label ), NITOROL (15 Mg/d) (View Nitorol Review and Nitorol Label ), MAGNESIUM OXIDE (2 G/d) (View Magnesium Oxide Review and Magnesium Oxide Label ), CLARITHROMYCIN (200 Mg/d) (View Clarithromycin Review and Clarithromycin Label ), EPINASTINE HYDROCHLORIDE (20 Mg/d) (View Epinastine Hydrochloride Review and Epinastine Hydrochloride Label ), LAMISIL (125 Mg/d) (View Lamisil Review and Lamisil Label ), WARFARIN POTASSIUM (2.5 Mg/d) (View Warfarin Potassium Review and Warfarin Potassium Label ). Patient was hospitalized.


5234283-5 | Alanine Aminotransferase Increased, Aspartate Aminotransferase Increased, Bacteraemia, Bacterial Infection, Blood Alkaline Phosphatase Increased, Blood Bilirubin Increased, Blood Bilirubin Unconjugated Increased, Blood Creatinine Increased, Blood Pressure Decreased
on Feb 05, 2007 Male patient from JAPAN , 81 years of age, was diagnosed with seborrhoeic dermatitis, atrial fibrillation (What is atrial fibrillation?), constipation (What is constipation?), nail tinea, cerebral infarction and was treated with Tofisopam (View Usage). Patient had the following side effects: alanine aminotransferase increased, aspartate aminotransferase increased, bacteraemia, bacterial infection (What is bacterial infection?), blood alkaline phosphatase increased, blood bilirubin increased, blood bilirubin unconjugated increased, blood creatinine increased, blood pressure decreased. Tofisopam dosage: 150 Mg/d. During the same period patient was treated with HIBON (60 Mg/d) (View Hibon Review and Hibon Label ), FUJISMIN (90 Mg/d) (View Fujismin Review and Fujismin Label ), NITOROL (15 Mg/d) (View Nitorol Review and Nitorol Label ), MAGNESIUM OXIDE (2 G/d) (View Magnesium Oxide Review and Magnesium Oxide Label ), CLARITHROMYCIN (200 Mg/d) (View Clarithromycin Review and Clarithromycin Label ), EPINASTINE HYDROCHLORIDE (20 Mg/d) (View Epinastine Hydrochloride Review and Epinastine Hydrochloride Label ), LAMISIL (125 Mg/d) (View Lamisil Review and Lamisil Label ), WARFARIN POTASSIUM (2.5 Mg/d) (View Warfarin Potassium Review and Warfarin Potassium 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 Tofisopam 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 Tofisopam quality problem: suspected counterfeit product, potentially contaminated product indicated by suspicious odor or unusual color, inaccurate or unreadable product labeling
3. Potential Tofisopam 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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Tofisopam Reactions
Alanine Aminotransferase Increased
Aspartate Aminotransferase Increased
Bacteraemia
Bacterial InfectionWhat is Bacterial infection?
Blood Alkaline Phosphatase Increased
Blood Bilirubin Increased
Blood Bilirubin Unconjugated Increased
Blood Creatinine Increased
Blood Pressure Decreased
Tofisopam 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 Tofisopam 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!