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Namenda (Memantine) - Death - Suspected Cause - Side Effect Reports

 
 



Index of reports > Death (4)

Below is the selection of side effect reports (a.k.a. adverse event reports) related to Namenda (Memantine) death. The selected reports were submitted to the FDA during the sample period of about a year.

Possible Namenda side effects in male

Reported by a physician from United States on 2011-12-15

Patient: male

Reactions: Haemorrhage Intracranial

Adverse event resulted in: death, hospitalization

Drug(s) suspected as cause:
Namenda



Possible Namenda side effects in male

Reported by a pharmacist from United States on 2011-12-09

Patient: male

Reactions: Drug Level Increased, Myocardial Infarction

Adverse event resulted in: death

Drug(s) suspected as cause:
Namenda

Other drugs received by patient: Donepezil HCL; Quetiapine Fumarate; Pioglitazone; Darifenacin; Sitagliptin



Possible Namenda side effects in male

Reported by a pharmacist from United States on 2011-12-02

Patient: male

Reactions: Drug Level Increased, Myocardial Infarction

Adverse event resulted in: death

Drug(s) suspected as cause:
Namenda

Other drugs received by patient: Sitagliptin (Sitagliptin) (Sitagliptin); Quetiapine (Quetiapine) (Quetiapine); Donepezil (Donepezil) (Donepezil); Pioglitazone (Pioglitazone) (Pioglitazone); Darifenacin (Darifenacin) (Darifenacin)



Possible Namenda side effects in female

Reported by a physician from United States on 2011-11-04

Patient: female, weighing 56.7 kg (124.7 pounds)

Reactions: Chest Discomfort, Bundle Branch Block Left, Concomitant Disease Progression, Loss of Consciousness, Chest Pain, Dizziness, Acute Myocardial Infarction, Shock

Adverse event resulted in: death, life threatening event, hospitalization

Drug(s) suspected as cause:
Namenda
    Dosage: 10 mg, bid
    Administration route: Oral
    Indication: Dementia Alzheimer's Type
    Start date: 2007-02-13
    End date: 2007-05-13

Exelon
    Dosage: 3 mg, bid
    Administration route: Oral
    Indication: Dementia Alzheimer's Type
    Start date: 2007-02-13
    End date: 2007-05-13

Other drugs received by patient: Warfarin Sodium; Toprol-XL; Lisinopril

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