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Micardis HCT (Telmisartan / Hydrochlorothiazide) - Death - Suspected Cause - Side Effect Reports

 
 



Index of reports > Death (7)

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

Possible Micardis HCT side effects in 89 year old female

Reported by a consumer/non-health professional from Peru on 2012-08-21

Patient: 89 year old female

Reactions: Sepsis, Urinary Tract Infection

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

Drug(s) suspected as cause:
Micardis HCT
    Dosage: strength:80+12.5mg; daily dose:80+12.5mg
    Administration route: Oral
    Indication: Hypertension
    Start date: 2010-01-01
    End date: 2012-07-01

Spiriva
    Dosage: 18 mcg
    Indication: Chronic Obstructive Pulmonary Disease
    Start date: 2010-01-01
    End date: 2012-07-01



Possible Micardis HCT side effects in 64 year old female

Reported by a consumer/non-health professional from Peru on 2012-08-20

Patient: 64 year old female

Reactions: Cerebrovascular Accident

Adverse event resulted in: death

Drug(s) suspected as cause:
Micardis HCT



Possible Micardis HCT side effects in female

Reported by a physician from Mexico on 2012-08-13

Patient: female

Reactions: Platelet Count Decreased, Upper Gastrointestinal Haemorrhage

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

Drug(s) suspected as cause:
Dabigatran Etexilate
    Dosage: 110 mg
    Administration route: Oral
    Indication: Cerebrovascular Accident Prophylaxis
    Start date: 2012-06-01
    End date: 2012-07-01

Micardis HCT
    Dosage: strength: 80/12.5mg daily dose: one tablet daily
    Administration route: Oral
    Indication: Hypertension
    Start date: 2012-04-01
    End date: 2012-07-01



Possible Micardis HCT side effects in 81 year old female

Reported by a consumer/non-health professional from Brazil on 2012-03-23

Patient: 81 year old female

Reactions: Respiratory Arrest

Adverse event resulted in: death

Drug(s) suspected as cause:
Micardis HCT



Possible Micardis HCT side effects in 69 year old female

Reported by a consumer/non-health professional from Germany on 2012-03-06

Patient: 69 year old female

Reactions: Petechiae, Pancytopenia, Aplastic Anaemia, Asthenia

Adverse event resulted in: death, hospitalization

Drug(s) suspected as cause:
Acetaminophen
    Administration route: Oral
    Start date: 2010-01-01
    End date: 2010-07-14

Allopurinol
    Indication: Hyperuricaemia
    Start date: 2010-03-01
    End date: 2010-07-14

Analgilasa
    Administration route: Oral
    Indication: Osteoarthritis
    Start date: 2009-11-01
    End date: 2010-07-14

Diclofenac Sodium
    Administration route: Oral
    Start date: 2009-01-01
    End date: 2010-01-01

Dipyrone TAB
    Start date: 2009-10-01
    End date: 2010-01-01

Furosemide
    Administration route: Oral
    Start date: 2010-01-01
    End date: 2010-07-11

Lovaza
    Administration route: Oral
    Start date: 2010-01-01
    End date: 2010-07-14

Micardis HCT
    Administration route: Oral
    Indication: Hypertension
    Start date: 2010-03-01
    End date: 2010-07-14

Omeprazole
    Administration route: Oral
    Indication: Gastric Ulcer
    Start date: 2009-11-01
    End date: 2010-07-14

Other drugs received by patient: Vancomycin; Meropenem; Nitroglycerin; Ambisome; Piperacillin and Tazobactam; Linezolid



Possible Micardis HCT side effects in 65 year old male

Reported by a consumer/non-health professional from Brazil on 2011-11-18

Patient: 65 year old male

Reactions: Infarction

Adverse event resulted in: death

Drug(s) suspected as cause:
Micardis HCT



Possible Micardis HCT side effects in 81 year old female

Reported by a health professional (non-physician/pharmacist) from France on 2011-10-03

Patient: 81 year old female

Reactions: Confusional State, Agitation, Blood Creatine Phosphokinase Increased, Hyponatraemia, Coma, Delirium, Blood Creatinine Increased

Adverse event resulted in: death, hospitalization

Drug(s) suspected as cause:
Acetaminophen with Propoxyphene HCL TAB
    Administration route: Oral
    Start date: 2008-11-08
    End date: 2008-11-17

Lyrica
    Administration route: Oral
    Indication: Neuralgia
    Start date: 2008-11-08
    End date: 2008-11-17

Micardis HCT
    Dosage: 80mg/12.5mg
    Start date: 2008-05-06
    End date: 2008-11-20

Other drugs received by patient: Rosuvastatin; Levothyroxine; Aspirin; Micardis HCT; Betaxolol; Dextropropoxyphene Hydrochloride

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