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Altace (Ramipril) - Adverse Event Reports - Life Threatening Events - Angioedema

 



Index of reports > Cases resulting in life threatening events (18) > Cases with Angioedema (3)

Below is the selection of adverse event reports related to Altace (Ramipril) that includes cases resulting in life threatening events where reactions include angioedema.

Adverse event in receiving Altace (Ramipril)

Reported by a consumer/non-health professional from United States on 2007-03-21

Patient:

Adverse reactions / side effects: Atelectasis, Blood Pressure Increased, Angioedema, Tongue Oedema, Tachycardia, Blood PH Decreased, Acidosis, Blood Bicarbonate Decreased, Asphyxia, Pco2 Increased, Face Oedema, Lung Disorder, Pharyngeal Oedema

Adverse event resulted in: life threatening event, hospitalization

Suspect drug(s):
Altace
    Dosage: 2.5 mg, qd
    Administration route: Oral
    Indication: Essential Hypertension
    Start date: 2005-12-16
    End date: 2006-01-01

Altace
    Dosage: 5 mg, qd
    Administration route: Oral
    Start date: 2006-01-01
    End date: 2006-12-01

Other drugs received by patient: Estracyt / 00327002 /; Anafranil; Dicetel / 00505101 /; Seresta; Noctamid; Tahor; Mupiderm



Adverse event in receiving Altace (Ramipril)

Reported by a physician from Canada on 2007-02-23

Patient:

Adverse reactions / side effects: Angioedema, Face Oedema, Pharyngeal Oedema, Dysphonia, Swollen Tongue, Unevaluable Event

Adverse event resulted in: life threatening event, hospitalization

Suspect drug(s):
Altace
    Dosage: 10 mg, qd
    Administration route: Oral
    Indication: Blood Pressure
    Start date: 2000-01-01
    End date: 2006-07-01

Crestor
    Dosage: 20 mg, qd
    Administration route: Oral
    Indication: Blood Cholesterol Increased
    Start date: 2001-01-01
    End date: 2006-12-03

Other drugs received by patient: Aspirin; Multi-Vitamins; Calcium Citrate W / Vitamin D NOS; Hydrodiuril; Plavix; Adalat; Doxepin HCL; Epipen



Adverse event in receiving Altace (Ramipril)

Reported by a physician from Canada on 2007-02-01

Patient:

Adverse reactions / side effects: Angioedema, Face Oedema, Pharyngeal Oedema, Dysphonia, Swollen Tongue

Adverse event resulted in: life threatening event, hospitalization

Suspect drug(s):
Altace
    Dosage: 10 mg, qd
    Administration route: Oral
    Indication: Blood Pressure
    Start date: 2000-01-01
    End date: 2006-07-01

Crestor
    Dosage: 20 mg, qd
    Administration route: Oral
    Indication: Blood Cholesterol Increased
    Start date: 2001-01-01
    End date: 2006-12-03

Other drugs received by patient: Aspirin; Multi-Vitamins; Calcium Citrate W / Vitamin D NOS; Hydrodiuril

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