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Index of reports
> Cases with Hyperkalaemia ()
Below is the selection of side effect reports (a.k.a. adverse event reports) related to Micardis (Telmisartan) where reactions include hyperkalaemia. The selected reports were submitted to the FDA during the sample period of about a year.
Possible Micardis side effects in 71 year old female
Reported by a physician from Switzerland on 2012-04-26
Patient: 71 year old female, weighing 60.0 kg (132.0 pounds)
Reactions: Vomiting, Hyperkalaemia, Nausea, General Physical Health Deterioration, Hypokalaemia, Acidosis Hyperchloraemic, Diarrhoea, Glycosuria, Proteinuria, Oliguria, Albuminuria, Haemodialysis-Induced Symptom, Renal Tubular Necrosis, Renal Failure Acute
Adverse event resulted in: hospitalization
Drug(s) suspected as cause:
Truvada
Administration route: Oral
Indication: HIV Infection
Start date: 2011-08-01
End date: 2012-03-06
Micardis
Administration route: Oral
Indication: Product Used FOR Unknown Indication
End date: 2012-03-06
Norvir
Administration route: Oral
Indication: HIV Infection
Start date: 2011-08-01
End date: 2012-03-06
Other drugs received by patient: Acetaminophen; Marcumar; Darunavir; Hydrocortisone; Zolpidem Tartrate; Boniva; Pantoprazole Sodium Sesquihydrate
Possible Micardis side effects in female
Reported by a physician from Japan on 2012-02-23
Patient: female
Reactions: Renal Impairment, Hyperkalaemia, Depressed Level of Consciousness, Sinus Arrest
Adverse event resulted in: hospitalization
Drug(s) suspected as cause:
Micardis
Other drugs received by patient: Alendronate Sodium; Magnesium Sulfate; Amlodipine
Possible Micardis side effects in 60 year old male
Reported by a physician from Switzerland on 2011-12-13
Patient: 60 year old male
Reactions: Metabolic Acidosis, Hyperkalaemia, Renal Failure Acute
Adverse event resulted in: hospitalization
Drug(s) suspected as cause:
Spironolactone
Indication: Hepatic Cirrhosis
Spironolactone
Dosage: 100 mg
Administration route: Oral
Indication: Hepatic Fibrosis
Start date: 2011-01-01
End date: 2011-10-20
Micardis
Dosage: 80 mg
Administration route: Oral
End date: 2011-10-20
Possible Micardis side effects in 84 year old female
Reported by a physician from Japan on 2011-12-01
Patient: 84 year old female
Reactions: Hyperkalaemia, Drug Interaction, Blood Creatinine Increased
Adverse event resulted in: life threatening event
Drug(s) suspected as cause:
Aldactone
Indication: Cardiac Failure Chronic
Aldactone
Administration route: Oral
Indication: Hypertension
Micardis
Administration route: Oral
Indication: Hypertension
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