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Zantac (Ranitidine) - Adverse Event Reports - Death

 



Index of reports > Cases resulting in death (7)

     Adrenal Cortical Insufficiency (2)Lung Abscess (2)Interstitial Lung Disease (2)Cardiac Arrest (2)Adrenocortical Insufficiency Acute (1)Chills (1)Respiratory Depression (1)Convulsion (1)Asthenia (1)

Below is the selection of adverse event reports related to Zantac (Ranitidine) that includes cases resulting in death.

Adverse event in male receiving Zantac (Ranitidine)

Reported by a physician from Japan on 2007-10-30

Patient: male

Adverse reactions / side effects: Interstitial Lung Disease, Respiratory Failure, Lung Abscess

Adverse event resulted in: death

Suspect drug(s):
Finibax

Finibax
    Indication: Lung Abscess

Norvasc
    Administration route: Oral
    Indication: Drug USE FOR Unknown Indication

Itraconazole
    Administration route: Oral
    Indication: Drug USE FOR Unknown Indication

Zantac
    Administration route: Oral
    Indication: Drug USE FOR Unknown Indication

Ferromia
    Administration route: Oral
    Indication: Drug USE FOR Unknown Indication

Erythrocin
    Administration route: Oral
    Indication: Drug USE FOR Unknown Indication

Biofermin R
    Administration route: Oral
    Indication: Drug USE FOR Unknown Indication

Sucralfate
    Administration route: Oral
    Indication: Drug USE FOR Unknown Indication

Slow-K
    Administration route: Oral
    Indication: Drug USE FOR Unknown Indication

Mucosta
    Administration route: Oral
    Indication: Drug USE FOR Unknown Indication

Juzen-Taiho-TO
    Administration route: Oral
    Indication: Drug USE FOR Unknown Indication

Other drugs received by patient: Cravit



Adverse event in male receiving Zantac (Ranitidine)

Reported by a physician from Japan on 2007-10-19

Patient: male

Adverse reactions / side effects: Interstitial Lung Disease, Lung Abscess

Adverse event resulted in: death, life threatening event

Suspect drug(s):
Finibax

Finibax
    Indication: Lung Abscess

Norvasc
    Administration route: Oral
    Indication: Drug USE FOR Unknown Indication

Itraconazole
    Administration route: Oral
    Indication: Drug USE FOR Unknown Indication

Zantac
    Administration route: Oral
    Indication: Drug USE FOR Unknown Indication

Ferromia
    Administration route: Oral
    Indication: Drug USE FOR Unknown Indication

Erythrocin Lactobionate
    Administration route: Oral
    Indication: Drug USE FOR Unknown Indication

Biofermin R
    Administration route: Oral
    Indication: Drug USE FOR Unknown Indication

Sucralfate
    Administration route: Oral
    Indication: Drug USE FOR Unknown Indication

Slow-K
    Administration route: Oral
    Indication: Drug USE FOR Unknown Indication

Mucosta
    Administration route: Oral
    Indication: Drug USE FOR Unknown Indication

Juzen-Taiho-TO
    Administration route: Oral
    Indication: Drug USE FOR Unknown Indication

Other drugs received by patient: Levofloxacin



Adverse event in 58 year old female receiving Zantac (Ranitidine)

Reported by a consumer/non-health professional from France on 2007-04-20

Patient: 58 year old female, weighing 95.0 kg (209.0 pounds)

Adverse reactions / side effects: Abdominal Pain, Hepatic Necrosis, Mydriasis, Anaphylactic Shock, Livedo Reticularis, Erythema, Paraesthesia, Loss of Consciousness, Syncope, Renal Impairment, Cardiac Arrest, Anuria

Adverse event resulted in: death, hospitalization

Suspect drug(s):
Zantac
    Dosage: 25mg single dose
    Start date: 2007-03-09
    End date: 2007-03-09

Zantac
    Dosage: 25mg single dose
    Start date: 2007-02-09
    End date: 2007-02-09

Polaramine
    Dosage: 2.5mg single dose
    Start date: 2007-03-09
    End date: 2007-03-09

Other drugs received by patient: Polaramine; Taxol; Herceptin; Carboplatin; Solu-Medrol



Adverse event in 57 year old female receiving Zantac (Ranitidine)

Reported by a individual with unspecified qualification from Germany on 2007-04-10

Patient: 57 year old female

Adverse reactions / side effects: Myoclonus, Overdose, Bradypnoea, Miosis, Drug Interaction, Respiratory Depression, Hyperhidrosis, Somnolence

Adverse event resulted in: death, life threatening event

Suspect drug(s):
Zantac
    Dosage: unk / unknown / injection

Morphine
    Dosage: unk / unknown / intravenous

Other drugs received by patient: Paclitaxel; ME-Prednisolone NA Succ.; Dexchlorpheniram.maleate; Alprazolam; Amitriptyline HCL; Gabapentin; Esomeprazole Magnesium; Ondansetron HCL; Metoclopramide HCL



Adverse event in 56 year old female receiving Zantac (Ranitidine)

Reported by a physician from Cameroon on 2007-03-26

Patient: 56 year old female

Adverse reactions / side effects: Chills, Delirium, Asthenia, Convulsion

Adverse event resulted in: death

Suspect drug(s):
Zantac (Ranitidine)

Other drugs received by patient: Metronidazole; Acetaminophen; Cephalosporin



Adverse event in 33 year old female receiving Zantac (Ranitidine)

Reported by a consumer/non-health professional from Sweden on 2007-02-02

Patient: 33 year old female

Adverse reactions / side effects: Vomiting, Adrenocortical Insufficiency Acute, Diarrhoea, Adrenal Cortical Insufficiency, Gastroenteritis, Blood Potassium Increased, Sudden Death, Cardiac Arrest

Adverse event resulted in: death

Suspect drug(s):
Betapred
    Administration route: Oral
    Indication: Iritis

Zantac
    Dosage: 600mg per day
    Administration route: Oral
    Indication: Gastritis
    Start date: 2005-11-07

Reductil
    Dosage: 10mg per day
    Administration route: Oral
    Indication: Obesity
    Start date: 2005-12-13



Adverse event in 33 year old female receiving Zantac (Ranitidine)

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

Patient: 33 year old female

Adverse reactions / side effects: Adrenal Cortical Insufficiency, Sudden Death

Adverse event resulted in: death

Suspect drug(s):
Betapred
    Dosage: 2.5mg per day
    Administration route: Oral
    Indication: Iritis

Zantac
    Dosage: 600mg per day
    Administration route: Oral
    Indication: Gastritis
    Start date: 2005-11-07

Reductil
    Dosage: 10mg per day
    Administration route: Oral
    Indication: Obesity
    Start date: 2005-12-13

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