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Zantac (Ranitidine) - Adverse Event Reports - Life Threatening Events - Shock

 



Index of reports > Cases resulting in life threatening events (25) > Cases with Shock (5)

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

Adverse event in 65 year old female receiving Zantac (Ranitidine)

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

Patient: 65 year old female

Adverse reactions / side effects: Cardio-Respiratory Arrest, Vomiting, Cyanosis, Angiopathy, Pallor, Cough, Shock

Adverse event resulted in: life threatening event

Suspect drug(s):
Zantac
    Dosage: 50mg per day
    Indication: Fallopian Tube Cancer
    Start date: 2006-12-07
    End date: 2007-04-05

Kytril
    Dosage: 3mg per day
    Indication: Fallopian Tube Cancer
    Start date: 2006-12-07
    End date: 2007-04-05

Other drugs received by patient: Decadron; Vena; Sodium Chloride 0.9%; Veen-D; Bosmin



Adverse event in 65 year old female receiving Zantac (Ranitidine)

Reported by a physician from Japan on 2007-05-22

Patient: 65 year old female

Adverse reactions / side effects: Cardio-Respiratory Arrest, Vomiting, Cyanosis, Pallor, Cough, Shock

Adverse event resulted in: life threatening event

Suspect drug(s):
Zantac
    Dosage: 50mg per day
    Indication: Drug USE FOR Unknown Indication
    Start date: 2006-12-07
    End date: 2007-04-05

Kytril
    Dosage: 3mg per day
    Indication: Drug USE FOR Unknown Indication
    Start date: 2006-12-07
    End date: 2007-04-05

Other drugs received by patient: Decadron; Vena; Sodium Chloride 0.9%; Veen-D; Bosmin



Adverse event in 65 year old male receiving Zantac (Ranitidine)

Reported by a physician from Japan on 2007-04-19

Patient: 65 year old male

Adverse reactions / side effects: Cardio-Respiratory Arrest, Shock

Adverse event resulted in: life threatening event

Suspect drug(s):
Zantac (Ranitidine)

Other drugs received by patient: Kytril; Decadron



Adverse event in 77 year old female receiving Zantac (Ranitidine)

Reported by a physician from Japan on 2007-04-02

Patient: 77 year old female, weighing 55.0 kg (121.0 pounds)

Adverse reactions / side effects: Urinary Incontinence, Hypotension, Cyanosis, Palpitations, Depressed Level of Consciousness, Cold Sweat, Shock, Oxygen Saturation Decreased

Adverse event resulted in: life threatening event, hospitalization

Suspect drug(s):
Zantac
    Dosage: 8ml per day
    Indication: Premedication
    Start date: 2007-02-22
    End date: 2007-02-22

Decadron
    Dosage: 8ml per day
    Indication: Premedication
    Start date: 2007-02-22
    End date: 2007-02-22

Restamin
    Dosage: 5tab per day
    Administration route: Oral
    Indication: Premedication
    Start date: 2007-02-22
    End date: 2007-02-27

Other drugs received by patient: Solita-T No.3



Adverse event in 87 year old female receiving Zantac (Ranitidine)

Reported by a physician from Japan on 2007-03-29

Patient: 87 year old female, weighing 38.0 kg (83.6 pounds)

Adverse reactions / side effects: Blood Creatine Phosphokinase Increased, Rhabdomyolysis, Delirium, Anorexia, Depressed Level of Consciousness, Renal Failure Acute, Shock, White Blood Cell Count Increased

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

Suspect drug(s):
Allopurinol
    Dosage: 100mg per day
    Administration route: Oral
    Start date: 2007-02-08

Zantac
    Dosage: 150mg per day
    Administration route: Oral
    Start date: 2007-02-08

Other drugs received by patient: Renivace; Artist; Amlodin; Unknown Medication

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