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Index of reports
> Cases resulting in other serious reactions (94)
Below is the selection of adverse event reports related to Micardis (Telmisartan) that includes cases resulting in other serious reactions.
Reports 1 - 25 of 94 Next >>
Adverse event in female receiving Micardis (Telmisartan)
Reported by a physician from Japan on 2007-10-31
Patient: female, weighing 38.0 kg (83.6 pounds)
Adverse reactions / side effects: Myoglobinaemia
Suspect drug(s):
Micardis (Telmisartan)
Other drugs received by patient: Coniel; Excegran
Adverse event in male receiving Micardis (Telmisartan)
Reported by a individual with unspecified qualification from Japan on 2007-10-25
Patient: male, weighing 58.0 kg (127.6 pounds)
Adverse reactions / side effects: Renal Failure Chronic
Adverse event resulted in: disablity
Suspect drug(s):
Micardis (Telmisartan)
Other drugs received by patient: Candesartan Cilexetil; Doxazosin Mesylate; Artist; Ticlopidine HCL; Norvasc; Adalat
Adverse event in male receiving Micardis (Telmisartan)
Reported by a individual with unspecified qualification from Japan on 2007-10-23
Patient: male, weighing 73.9 kg (162.6 pounds)
Adverse reactions / side effects: Gastric Cancer
Adverse event resulted in: hospitalization
Suspect drug(s):
Micardis (Telmisartan)
Other drugs received by patient: Novorapid MIX; Lantus; Dibetos; Basen; Lipitor; Glufast
Adverse event in female receiving Micardis (Telmisartan)
Reported by a individual with unspecified qualification from Japan on 2007-10-23
Patient: female, weighing 43.0 kg (94.6 pounds)
Adverse reactions / side effects: Adverse Event
Suspect drug(s):
Micardis (Telmisartan)
Adverse event in male receiving Micardis (Telmisartan)
Reported by a individual with unspecified qualification from United Kingdom on 2007-10-19
Patient: male, weighing 108.0 kg (237.6 pounds)
Adverse reactions / side effects: Duodenitis, Duodenal Ulcer
Suspect drug(s):
Aggrenox
Dosage: twice a day
Administration route: Oral
Indication: Cerebrovascular Accident Prophylaxis
Start date: 2004-02-26
End date: 2007-08-23
Micardis
Dosage: 1 daily
Administration route: Oral
Indication: Cerebrovascular Accident Prophylaxis
Start date: 2004-02-26
Clopidogrel
Administration route: Oral
Indication: Cerebrovascular Accident Prophylaxis
Start date: 2004-02-26
Adverse event in male receiving Micardis (Telmisartan)
Reported by a individual with unspecified qualification from United States on 2007-10-18
Patient: male, weighing 94.0 kg (206.8 pounds)
Adverse reactions / side effects: Aortic Dilatation, Hypertension
Suspect drug(s):
Micardis
Administration route: Oral
Indication: Cardiovascular Disorder
Start date: 2002-11-15
Micardis
Indication: Cerebrovascular Accident Prophylaxis
Other drugs received by patient: Niaspan; Toprol-XL; Zocor; Ecotrin; Allegra; Azopt; Prevacid; Lumigan; Lexapro; Alphagan
Adverse event in male receiving Micardis (Telmisartan)
Reported by a individual with unspecified qualification from United States on 2007-10-18
Patient: male, weighing 94.0 kg (206.8 pounds)
Adverse reactions / side effects: Aortic Dilatation, Hypertension
Suspect drug(s):
Micardis
Administration route: Oral
Indication: Cardiovascular Disorder
Start date: 2002-11-15
Micardis
Indication: Cerebrovascular Accident Prophylaxis
Other drugs received by patient: Niaspan; Toprol-XL; Zocor; Ecotrin; Allegra; Azopt; Prevacid; Lumigan; Lexapro; Alphagan
Adverse event in male receiving Micardis (Telmisartan)
Reported by a individual with unspecified qualification from United States on 2007-10-18
Patient: male, weighing 94.0 kg (206.8 pounds)
Adverse reactions / side effects: Aortic Dilatation, Hypertension
Suspect drug(s):
Micardis
Administration route: Oral
Indication: Cardiovascular Disorder
Start date: 2002-11-15
Micardis
Indication: Cerebrovascular Accident Prophylaxis
Other drugs received by patient: Niaspan; Toprol-XL; Zocor; Ecotrin; Allegra; Azopt; Prevacid; Lumigan; Lexapro; Alphagan
Adverse event in male receiving Micardis (Telmisartan)
Reported by a individual with unspecified qualification from Japan on 2007-10-16
Patient: male, weighing 61.0 kg (134.2 pounds)
Adverse reactions / side effects: Neoplasm Malignant, Blood Pressure Decreased
Suspect drug(s):
Micardis (Telmisartan)
Adverse event in 78 year old female receiving Micardis (Telmisartan)
Reported by a health professional (non-physician/pharmacist) from United States on 2007-10-12
Patient: 78 year old female, weighing 118.6 kg (261.0 pounds)
Adverse reactions / side effects: Rash Generalised, Urticaria, Liver Function Test Abnormal, Rash Pruritic
Suspect drug(s):
Micardis (Telmisartan)
Other drugs received by patient: Furosemide
Adverse event in male receiving Micardis (Telmisartan)
Reported by a individual with unspecified qualification from Japan on 2007-10-09
Patient: male
Adverse reactions / side effects: Lung Neoplasm Malignant
Adverse event resulted in: hospitalization
Suspect drug(s):
Micardis (Telmisartan)
Adverse event in male receiving Micardis (Telmisartan)
Reported by a individual with unspecified qualification from Japan on 2007-10-09
Patient: male, weighing 66.0 kg (145.2 pounds)
Adverse reactions / side effects: Weight Decreased, Gastric Cancer
Suspect drug(s):
Micardis (Telmisartan)
Adverse event in male receiving Micardis (Telmisartan)
Reported by a individual with unspecified qualification from Japan on 2007-10-08
Patient: male
Adverse reactions / side effects: Gastric Cancer
Suspect drug(s):
Micardis (Telmisartan)
Adverse event in male receiving Micardis (Telmisartan)
Reported by a individual with unspecified qualification from Japan on 2007-10-04
Patient: male, weighing 66.0 kg (145.2 pounds)
Adverse reactions / side effects: Weight Decreased, Gastric Cancer
Suspect drug(s):
Micardis (Telmisartan)
Adverse event in male receiving Micardis (Telmisartan)
Reported by a individual with unspecified qualification from Japan on 2007-10-03
Patient: male
Adverse reactions / side effects: Adverse Event
Suspect drug(s):
Micardis (Telmisartan)
Adverse event in 57 year old male receiving Micardis (Telmisartan)
Reported by a pharmacist from Japan on 2007-10-02
Patient: 57 year old male, weighing 59.0 kg (129.8 pounds)
Adverse reactions / side effects: White Blood Cell Count Decreased, Dyspnoea, Pericardial Effusion, Haemoglobin Decreased, Haematocrit Decreased, Thrombocytopenic Purpura, Platelet Count Decreased, Haemorrhagic Diathesis, Rash Maculo-Papular
Adverse event resulted in: life threatening event
Suspect drug(s):
Lasix
Dosage: 20 mg/day
Administration route: Oral
Indication: Cardiac Failure Congestive
Start date: 2007-06-12
End date: 2007-07-13
Aldactone
Dosage: 25 mg/day
Administration route: Oral
Indication: Cardiac Failure Congestive
Start date: 2007-06-27
End date: 2007-07-20
Tenormin
Dosage: 25 mg/day
Administration route: Oral
Indication: Atrial Fibrillation
Start date: 2004-04-01
End date: 2007-07-20
Micardis
Dosage: 20 mg/day
Administration route: Oral
Indication: Cardiac Failure Congestive
Start date: 2004-04-01
End date: 2007-07-20
Warfarin Sodium
Dosage: 3 mg/day
Administration route: Oral
Indication: Atrial Fibrillation
Start date: 2007-06-07
End date: 2007-07-09
Propylthiouracil
Dosage: 300 mg/day
Administration route: Oral
Start date: 1987-01-01
End date: 2007-07-12
Propylthiouracil
Dosage: 200 mg/day
Administration route: Oral
Start date: 2007-07-13
End date: 2007-07-20
Propylthiouracil
Dosage: 300 mg/day
Administration route: Oral
Start date: 2007-08-03
Mucosta
Dosage: 300 mg/day
Administration route: Oral
Indication: Gastric Mucosal Lesion
Start date: 2007-05-18
End date: 2007-07-13
Sigmart
Dosage: 15 mg/day
Administration route: Oral
Indication: Angina Pectoris
Start date: 2004-04-01
End date: 2007-07-13
Bepricor
Dosage: 150 mg/day
Administration route: Oral
Indication: Atrial Fibrillation
Start date: 2007-07-02
End date: 2007-07-20
Nitroderm
Dosage: 1 patch/day
Indication: Angina Pectoris
Start date: 2007-07-13
Amlodipine Besylate
Indication: Angina Pectoris
Start date: 2004-04-01
Aspirin
Dosage: 100mg
Administration route: Oral
End date: 2007-07-12
Other drugs received by patient: Unasyn; Gentacin
Adverse event in male receiving Micardis (Telmisartan)
Reported by a individual with unspecified qualification on 2007-10-02
Patient: male
Adverse reactions / side effects: Adverse Event
Suspect drug(s):
Micardis (Telmisartan)
Adverse event in female receiving Micardis (Telmisartan)
Reported by a individual with unspecified qualification from Japan on 2007-10-02
Patient: female, weighing 39.0 kg (85.8 pounds)
Adverse reactions / side effects: Gastric Cancer
Suspect drug(s):
Micardis (Telmisartan)
Adverse event in 57 year old male receiving Micardis (Telmisartan)
Reported by a pharmacist from Japan on 2007-07-31
Patient: 57 year old male
Adverse reactions / side effects: RED Blood Cell Count Increased, Haematocrit Increased, Haemoglobin Increased
Suspect drug(s):
Norvasc
Dosage: daily dose:10mg
Administration route: Oral
Amaryl
Dosage: daily dose:1mg
Administration route: Oral
Micardis
Dosage: daily dose:80mg
Administration route: Oral
Warfarin Sodium
Dosage: daily dose:3mg
Administration route: Oral
Omeprazole
Dosage: daily dose:20mg
Administration route: Oral
Anplag
Dosage: daily dose:300mg
Administration route: Oral
Mucosta
Administration route: Oral
Adverse event in female receiving Micardis (Telmisartan)
Reported by a individual with unspecified qualification from Japan on 2007-07-31
Patient: female, weighing 51.0 kg (112.2 pounds)
Adverse reactions / side effects: Acute Respiratory Distress Syndrome, Influenza
Adverse event resulted in: life threatening event, hospitalization
Suspect drug(s):
Micardis (Telmisartan)
Other drugs received by patient: Norvasc; Myslee; Rohypnol; Nelbis
Adverse event in female receiving Micardis (Telmisartan)
Reported by a individual with unspecified qualification from Japan on 2007-07-30
Patient: female, weighing 51.0 kg (112.2 pounds)
Adverse reactions / side effects: Cardiac Failure, Atrial Fibrillation, Blood Creatinine Increased
Adverse event resulted in: hospitalization
Suspect drug(s):
Micardis (Telmisartan)
Other drugs received by patient: Norvasc
Adverse event in 69 year old male receiving Micardis (Telmisartan)
Reported by a pharmacist from Japan on 2007-07-27
Patient: 69 year old male
Adverse reactions / side effects: Liver Disorder
Suspect drug(s):
Norvasc
Dosage: daily dose:5mg
Administration route: Oral
Indication: Hypertension
Micardis
Administration route: Oral
Indication: Hypertension
Start date: 2007-05-29
End date: 2007-07-12
Adverse event in female receiving Micardis (Telmisartan)
Reported by a physician from Japan on 2007-07-24
Patient: female, weighing 61.5 kg (135.3 pounds)
Adverse reactions / side effects: Hyperkalaemia, Bradyarrhythmia, Hypotension
Adverse event resulted in: life threatening event, hospitalization
Suspect drug(s):
Aldactone
Administration route: Oral
Indication: Cardiac Failure
Start date: 2007-02-01
End date: 2007-06-27
Micardis
Indication: Hypertension
Start date: 2005-01-01
End date: 2007-06-27
Other drugs received by patient: Amaryl; Basen; Aspirin; Lasix; Artist; Frandol; Magnesium Oxide
Adverse event in receiving Micardis (Telmisartan)
Reported by a consumer/non-health professional from United States on 2007-07-19
Patient:
Adverse reactions / side effects: Cardiac Failure
Suspect drug(s):
Micardis (Telmisartan)
Adverse event in female receiving Micardis (Telmisartan)
Reported by a individual with unspecified qualification from Japan on 2007-07-19
Patient: female, weighing 51.0 kg (112.2 pounds)
Adverse reactions / side effects: Cardiac Failure, Atrial Fibrillation, Blood Creatinine Increased
Adverse event resulted in: hospitalization
Suspect drug(s):
Micardis (Telmisartan)
Other drugs received by patient: Lasix; Norvasc
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