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Tenormin (Atenolol) - Adverse Event Reports - Life Threatening Events - Haematoma

 



Index of reports > Cases resulting in life threatening events (12) > Cases with Haematoma (3)

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

Adverse event in 71 year old female receiving Tenormin (Atenolol)

Reported by a physician from France on 2007-10-05

Patient: 71 year old female

Adverse reactions / side effects: Haematoma

Adverse event resulted in: life threatening event

Suspect drug(s):
Dafalgan
    Indication: Pain in Extremity

Pravadual Tabs
    Administration route: Oral
    Indication: Cardiac Disorder
    End date: 2007-04-16

Pravadual Tabs
    Administration route: Oral
    Indication: Hypertension
    End date: 2007-04-16

Previscan
    Administration route: Oral
    Indication: Cardiac Disorder
    End date: 2007-04-16

Previscan
    Administration route: Oral
    Indication: Hypertension
    End date: 2007-04-16

Tenormin
    Administration route: Oral
    End date: 2007-04-16

Augmentin '125'
    Administration route: Oral
    Indication: Varicose Ulceration
    Start date: 2007-04-12
    End date: 2007-04-16

Nureflex
    Administration route: Oral
    Indication: Pain in Extremity

Other drugs received by patient: Lamaline



Adverse event in 71 year old female receiving Tenormin (Atenolol)

Reported by a physician from France on 2007-06-08

Patient: 71 year old female

Adverse reactions / side effects: Haematoma

Adverse event resulted in: life threatening event

Suspect drug(s):
Dafalgan
    Indication: Pain in Extremity

Pravadual Tabs
    Administration route: Oral
    Indication: Cardiac Disorder
    End date: 2007-04-16

Pravadual Tabs
    Administration route: Oral
    Indication: Hypertension
    End date: 2007-04-16

Acetylsalicylic Acid SRT

Previscan
    Administration route: Oral
    Indication: Cardiac Disorder
    End date: 2007-04-16

Previscan
    Administration route: Oral
    Indication: Hypertension
    End date: 2007-04-16

Tenormin
    Administration route: Oral
    End date: 2007-04-16

Augmentin '125'
    Administration route: Oral
    Indication: Varicose Ulceration
    Start date: 2007-04-12
    End date: 2007-04-16

Nureflex
    Administration route: Oral
    Indication: Pain in Extremity

Other drugs received by patient: Lamaline



Adverse event in 71 year old female receiving Tenormin (Atenolol)

Reported by a consumer/non-health professional from France on 2007-06-07

Patient: 71 year old female

Adverse reactions / side effects: Mydriasis, International Normalised Ratio Abnormal, Pupils Unequal, Loss of Consciousness, Renal Failure, Brain Oedema, Nervous System Disorder, Haematoma

Adverse event resulted in: life threatening event

Suspect drug(s):
Augmentin '125'
    Administration route: Oral
    Indication: Erysipelas
    Start date: 2007-04-12
    End date: 2007-04-16

Previscan
    Administration route: Oral
    Indication: Hypertensive Heart Disease
    End date: 2007-04-16

Tenormin
    Administration route: Oral
    Indication: Essential Hypertension
    End date: 2007-04-16

Pravastatin
    Administration route: Oral
    Indication: Hypertensive Heart Disease
    End date: 2007-04-16

Acetylsalicylic Acid SRT
    Administration route: Oral
    Indication: Hypertensive Heart Disease
    End date: 2007-04-16

Nureflex
    Dosage: 300mg per day
    Administration route: Oral

Other drugs received by patient: Dafalgan; Atacand; Desloratadine; Lamaline; NON Steroidal Antiinflammatory

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