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Ranitidine (Ranitidine) - Adverse Event Reports - Life Threatening Events - Hypoxic Encephalopathy

 



Index of reports > Cases resulting in life threatening events (13) > Cases with Hypoxic Encephalopathy (2)

Below is the selection of adverse event reports related to Ranitidine that includes cases resulting in life threatening events where reactions include hypoxic encephalopathy.

Adverse event in 80 year old female receiving Ranitidine

Reported by a individual with unspecified qualification from United Kingdom on 2007-01-30

Patient: 80 year old female

Adverse reactions / side effects: Respiratory Arrest, Cardiac Arrest, Hypoxic Encephalopathy, Electromechanical Dissociation

Adverse event resulted in: life threatening event, hospitalization, disablity

Suspect drug(s):
Chlorpheniramine Maleate
    Dosage: 10 mg, intravenous
    Indication: Drug USE FOR Unknown Indication
    Start date: 2006-01-02

Ranitidine
    Dosage: 50 mg, intravenous
    Indication: Drug USE FOR Unknown Indication
    Start date: 2006-01-02



Adverse event in 80 year old female receiving Ranitidine

Reported by a consumer/non-health professional from United Kingdom on 2007-01-29

Patient: 80 year old female

Adverse reactions / side effects: Respiratory Arrest, Cardiac Arrest, Hypoxic Encephalopathy, Electromechanical Dissociation

Adverse event resulted in: life threatening event, hospitalization, disablity

Suspect drug(s):
Chlorpheniramine Maleate
    Dosage: 10mg unknown
    Indication: Drug USE FOR Unknown Indication
    Start date: 2006-01-02

Ranitidine
    Dosage: 50mg unknown
    Indication: Drug USE FOR Unknown Indication
    Start date: 2006-01-02

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