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Micardis (Telmisartan) - Adverse Event Reports - Other Serious Reactions - Dyspnoea

 



Index of reports > Cases resulting in other serious reactions (94) > Cases with Dyspnoea (6)

Below is the selection of adverse event reports related to Micardis (Telmisartan) that includes cases resulting in other serious reactions where reactions include dyspnoea.

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 75 year old male receiving Micardis (Telmisartan)

Reported by a physician from Japan on 2007-07-02

Patient: 75 year old male, weighing 52.5 kg (115.5 pounds)

Adverse reactions / side effects: Drug Eruption, Dyspnoea

Suspect drug(s):
Micardis
    Administration route: Oral
    Indication: Hypertension

Vesicare
    Administration route: Oral
    Indication: Hypertonic Bladder
    Start date: 2007-03-15
    End date: 2007-03-21

Other drugs received by patient: Harnal D (Tamsulosin Hydrochloride)



Adverse event in female receiving Micardis (Telmisartan)

Reported by a individual with unspecified qualification on 2007-06-19

Patient: female, weighing 83.9 kg (184.6 pounds)

Adverse reactions / side effects: Choking Sensation, Dyspnoea

Suspect drug(s):
Micardis (Telmisartan)

Other drugs received by patient: Flovent; Ventolin; Flonase



Adverse event in female receiving Micardis (Telmisartan)

Reported by a physician on 2007-05-24

Patient: female

Adverse reactions / side effects: Dyspnoea, Fibrin D Dimer Increased, Chest Pain, Pulmonary Thrombosis, Cardiomegaly

Adverse event resulted in: hospitalization

Suspect drug(s):
Micardis
    Start date: 2006-11-08

Spiriva

Other drugs received by patient: Advair Diskus 100 / 50; Clonazepam



Adverse event in female receiving Micardis (Telmisartan)

Reported by a individual with unspecified qualification on 2007-04-13

Patient: female, weighing 83.9 kg (184.6 pounds)

Adverse reactions / side effects: Choking Sensation, Dyspnoea

Suspect drug(s):
Micardis (Telmisartan)

Other drugs received by patient: Flovent; Ventolin; Flonase



Adverse event in female receiving Micardis (Telmisartan)

Reported by a individual with unspecified qualification on 2007-04-05

Patient: female, weighing 83.9 kg (184.6 pounds)

Adverse reactions / side effects: Choking Sensation, Dyspnoea

Suspect drug(s):
Micardis (Telmisartan)

Other drugs received by patient: Flovent; Ventolin; Flonase

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