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Zantac (Ranitidine) - Adverse Event Reports - All Cases

 



Index of reports > All cases (100)

     Vomiting (19)Hypersensitivity (11)Loss of Consciousness (10)Dyspnoea (9)Nausea (9)Shock (9)Medication Error (8)Mydriasis (7)Pallor (7)Pharmaceutical Product Complaint (6)

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

 Reports 1 - 25 of 100   Next >>

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 receiving Zantac (Ranitidine)

Reported by a pharmacist from United Kingdom on 2007-10-25

Patient:

Adverse reactions / side effects: Macular Degeneration

Suspect drug(s):
Zantac (Ranitidine)



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 2 month old male receiving Zantac (Ranitidine)

Reported by a consumer/non-health professional from United States on 2007-10-17

Patient: 2 month old male, weighing 5.4 kg (11.9 pounds)

Adverse reactions / side effects: Drug Exposure VIA Breast Milk, Erythema Multiforme

Suspect drug(s):
Zantac (Ranitidine)



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

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

Patient: 77 year old male

Adverse reactions / side effects: Agranulocytosis

Adverse event resulted in: hospitalization

Suspect drug(s):
Aspirin
    Dosage: total daily dose: 100 mg unit dose: 100 mg
    Administration route: Oral
    End date: 2007-06-11

Zantac
    Dosage: total daily dose: 150 mg unit dose: 150 mg
    Administration route: Oral
    End date: 2007-06-11

Lipitor
    Dosage: total daily dose: 10 mg unit dose: 10 mg
    Administration route: Oral
    End date: 2007-06-11

Tenormin
    Dosage: total daily dose: 50 mg unit dose: 50 mg
    Administration route: Oral
    End date: 2007-06-11

Pletal
    Administration route: Oral
    End date: 2007-06-11

Bepricor
    Administration route: Oral
    End date: 2007-06-11

Sigmart
    Administration route: Oral
    End date: 2007-06-11

Lendormin
    Administration route: Oral
    Indication: Insomnia
    End date: 2007-06-11

Warfarin Potassium
    Administration route: Oral
    End date: 2007-06-11

Other drugs received by patient: Lasix; Mucosolvan



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 66 year old female receiving Zantac (Ranitidine)

Reported by a physician from Japan on 2007-10-02

Patient: 66 year old female, weighing 58.0 kg (127.6 pounds)

Adverse reactions / side effects: Aplastic Anaemia, Bone Marrow Failure

Adverse event resulted in: hospitalization

Suspect drug(s):
Prograf
    Dosage: 3 mg, /d, oral
    Administration route: Oral
    Indication: Interstitial Lung Disease
    Start date: 2006-08-01
    End date: 2007-07-13

Zantac
    End date: 2007-07-13

Other drugs received by patient: Predonide (Prednisolone); Baktar (Sulfamethoxazole, Trimethoprim); Bonalon (Alendronic Acid); Panaldine (Ticlopidine Hydrochloride); Crestor



Adverse event in 43 year old male receiving Zantac (Ranitidine)

Reported by a pharmacist from United States on 2007-07-24

Patient: 43 year old male

Adverse reactions / side effects: Liver Function Test Abnormal

Adverse event resulted in: hospitalization

Suspect drug(s):
Zantac (Ranitidine)

Other drugs received by patient: Multi-Vitamin; Zofran; Promethazine; Insulin; Tylenol (Caplet); Risperidone; Oxycodone HCL; Colace; Heparin; Morphine



Adverse event in 45 year old male receiving Zantac (Ranitidine)

Reported by a pharmacist from United Kingdom on 2007-07-19

Patient: 45 year old male

Adverse reactions / side effects: Blood Creatine Phosphokinase Increased, Rhabdomyolysis

Adverse event resulted in: hospitalization

Suspect drug(s):
Floxapen
    Indication: Drug USE FOR Unknown Indication

Zantac
    Indication: Drug USE FOR Unknown Indication

Other drugs received by patient: Hydrocortisone; Ciprofloxacin



Adverse event in 59 year old female receiving Zantac (Ranitidine)

Reported by a individual with unspecified qualification from United States on 2007-07-13

Patient: 59 year old female

Adverse reactions / side effects: Intraocular Pressure Increased, Gastric Ulcer

Suspect drug(s):
Boniva
    Dosage: 150 mg oral
    Administration route: Oral
    Indication: Osteoporosis Postmenopausal
    Start date: 2006-08-15
    End date: 2007-02-15

Zantac

Other drugs received by patient: Xanax; Tums (Calcium Carbonate); Protonix



Adverse event in 64 year old female receiving Zantac (Ranitidine)

Reported by a physician from Japan on 2007-07-12

Patient: 64 year old female

Adverse reactions / side effects: C-Reactive Protein Increased, Pancytopenia, Pyrexia

Adverse event resulted in: hospitalization

Suspect drug(s):
Zantac (Ranitidine)

Other drugs received by patient: Omepral; Ciprofloxacin; Prodif; Vancomycin HCL; Vancomycin HCL; Maxipime; Gran; Predonine; Predonine



Adverse event in 12 year old female receiving Zantac (Ranitidine)

Reported by a consumer/non-health professional from Canada on 2007-07-10

Patient: 12 year old female

Adverse reactions / side effects: Personality Change, Affect Lability, Medication Error, Self-Injurious Ideation

Suspect drug(s):
Zantac (Ranitidine)



Adverse event in receiving Zantac (Ranitidine)

Reported by a consumer/non-health professional from Canada on 2007-07-10

Patient:

Adverse reactions / side effects: Intentional Overdose

Suspect drug(s):
Zantac (Ranitidine)



Adverse event in 90 year old male receiving Zantac (Ranitidine)

Reported by a individual with unspecified qualification from France on 2007-07-06

Patient: 90 year old male

Adverse reactions / side effects: Thrombocytopenia

Adverse event resulted in: hospitalization

Suspect drug(s):
Keppra
    Dosage: 1000 mg /d po
    Administration route: Oral
    End date: 2006-01-30

Zantac
    Dosage: 150 mg /d po
    Administration route: Oral
    End date: 2006-01-30

Allopurinol
    Dosage: 200 mg/d po
    Administration route: Oral
    End date: 2006-01-30

Paroxetine HCL
    Dosage: 20 mg /d po
    Administration route: Oral
    End date: 2006-02-03

Other drugs received by patient: Irbesartan; Synacthene; Depakene; Zolpidem Tartrate



Adverse event in 76 year old male receiving Zantac (Ranitidine)

Reported by a physician from Japan on 2007-07-06

Patient: 76 year old male

Adverse reactions / side effects: Neutrophil Count Decreased

Adverse event resulted in: hospitalization

Suspect drug(s):
Lipitor
    Dosage: daily dose:10mg
    Administration route: Oral

Aspirin
    Dosage: daily dose:100mg-freq:day
    Administration route: Oral
    Start date: 2007-04-27
    End date: 2007-06-10

Zantac
    Dosage: daily dose:150mg-freq:day
    Administration route: Oral
    Start date: 2007-04-27
    End date: 2007-06-10

Tenormin
    Dosage: daily dose:50mg-freq:day
    Administration route: Oral

Pletal
    Administration route: Oral

Bepricor
    Dosage: daily dose:100mg-freq:day
    Administration route: Oral
    Start date: 2007-04-27
    End date: 2007-06-10

Sigmart
    Dosage: daily dose:15mg-freq:day
    Administration route: Oral
    Start date: 2007-04-27
    End date: 2007-06-10

Lendormin
    Dosage: daily dose:.25mg-freq:day
    Administration route: Oral

Warfarin Sodium
    Dosage: daily dose:.5mg-freq:day
    Administration route: Oral
    Start date: 2007-04-27
    End date: 2007-06-10



Adverse event in 2 month old female receiving Zantac (Ranitidine)

Reported by a consumer/non-health professional from United States on 2007-07-02

Patient: 2 month old female

Adverse reactions / side effects: Overdose, Developmental Delay, Convulsion

Adverse event resulted in: hospitalization

Suspect drug(s):
Zantac (Ranitidine)

Other drugs received by patient: NO Concurrent Medication



Adverse event in male receiving Zantac (Ranitidine)

Reported by a physician from Japan on 2007-07-02

Patient: male

Adverse reactions / side effects: Neutrophil Count Decreased

Suspect drug(s):
Lipitor
    Dosage: daily dose:10mg
    Administration route: Oral

Atenolol
    Dosage: daily dose:50mg
    Administration route: Oral
    Indication: Cardiac Failure

Aspirin
    Dosage: daily dose:100mg
    Administration route: Oral
    Start date: 2007-04-27
    End date: 2007-06-10

Bepricor
    Dosage: daily dose:100mg
    Administration route: Oral
    Start date: 2007-04-27
    End date: 2007-06-10

Pletal
    Administration route: Oral

Sigmart
    Dosage: daily dose:15mg
    Administration route: Oral
    Start date: 2007-04-27
    End date: 2007-06-10

Warfarin Sodium
    Dosage: daily dose:.5mg
    Administration route: Oral
    Start date: 2007-04-27
    End date: 2007-06-10

Zantac
    Dosage: daily dose:150mg
    Administration route: Oral
    Start date: 2007-04-27
    End date: 2007-06-10

Lendormin
    Dosage: daily dose:.25mg-freq:frequency: prn
    Administration route: Oral

Other drugs received by patient: Furosemide; Ambroxol Hydrochloride



Adverse event in 20 year old female receiving Zantac (Ranitidine)

Reported by a health professional (non-physician/pharmacist) from France on 2007-07-02

Patient: 20 year old female

Adverse reactions / side effects: Neutropenia, Normochromic Normocytic Anaemia

Adverse event resulted in: hospitalization

Suspect drug(s):
Effexor
    Dosage: unknown
    Administration route: Oral
    End date: 2007-02-15

Rubozinc
    Dosage: unknown
    Administration route: Oral
    Start date: 2007-02-23
    End date: 2007-02-01

Zantac
    Dosage: unknown
    Administration route: Oral
    Start date: 2007-01-01
    End date: 2007-02-01

Other drugs received by patient: Atarax; Calcium Carbonate; Hept-A-MYL; Phocytan; Vitamin B1 and B6; Diffu K; Imodium; Tiorfan; Colecalciferol



Adverse event in male receiving Zantac (Ranitidine)

Reported by a physician from United States on 2007-06-28

Patient: male

Adverse reactions / side effects: Osteonecrosis

Adverse event resulted in: hospitalization

Suspect drug(s):
Enbrel
    Indication: Rheumatoid Arthritis
    Start date: 2004-01-01

Methotrexate
    Start date: 2006-10-01

Mobic
    Administration route: Oral
    Start date: 2006-10-01

Vicodin ES
    Start date: 2006-10-01

Zantac
    Start date: 2006-10-01

Lorazepam
    Start date: 2006-10-01



Adverse event in male receiving Zantac (Ranitidine)

Reported by a physician from Japan on 2007-06-28

Patient: male

Adverse reactions / side effects: Dyspnoea, Pulmonary Oedema, Myelodysplastic Syndrome, Pleural Effusion, Neutrophil Count Decreased

Suspect drug(s):
Tenormin
    Administration route: Oral
    Indication: Cardiac Failure
    End date: 2007-06-10

Aspirin
    Administration route: Oral
    Start date: 2007-04-27
    End date: 2007-06-10

Bepricor
    Administration route: Oral
    Start date: 2007-04-27
    End date: 2007-06-10

Lendormin
    Administration route: Oral
    End date: 2007-06-10

Lipitor
    Administration route: Oral
    End date: 2007-06-10

Pletal
    Administration route: Oral

Sigmart
    Administration route: Oral
    Start date: 2007-04-27
    End date: 2007-06-10

Warfarin Potassium
    Administration route: Oral
    Start date: 2007-04-27
    End date: 2007-06-10

Zantac
    Administration route: Oral
    Start date: 2007-04-27
    End date: 2007-06-10

Other drugs received by patient: Furosemide; Ambroxol Hydrochloride



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

Reported by a physician from Japan on 2007-06-26

Patient: 77 year old female, weighing 45.0 kg (99.0 pounds)

Adverse reactions / side effects: Rhabdomyolysis, Blood Creatine Phosphokinase Increased, Blood Lactate Dehydrogenase Increased, Alanine Aminotransferase Increased, Hypoaesthesia, Long QT Syndrome, Dysstasia, Convulsions Local, C-Reactive Protein Increased, Aspartate Aminotransferase Increased

Adverse event resulted in: life threatening event, hospitalization

Suspect drug(s):
Zantac (Ranitidine)

Other drugs received by patient: Cyanocobalamin; Vitamedin; Mucosta



Adverse event in 27 year old female receiving Zantac (Ranitidine)

Reported by a physician from Mexico on 2007-06-22

Patient: 27 year old female

Adverse reactions / side effects: Dyspnoea, Pruritus, Urticaria, Dizziness, Pharmaceutical Product Complaint

Suspect drug(s):
Zantac (Ranitidine)



Adverse event in 55 year old male receiving Zantac (Ranitidine)

Reported by a physician from Japan on 2007-06-22

Patient: 55 year old male

Adverse reactions / side effects: Blood Bilirubin Increased

Adverse event resulted in: hospitalization

Suspect drug(s):
Zantac (Ranitidine)



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

Reported by a pharmacist from Japan on 2007-06-21

Patient: 77 year old male

Adverse reactions / side effects: Neutropenia

Adverse event resulted in: hospitalization

Suspect drug(s):
Aspirin
    Dosage: total daily dose: 100 mg unit dose: 100 mg
    Administration route: Oral
    End date: 2007-06-11

Zantac
    Dosage: total daily dose: 150 mg unit dose: 150 mg
    Administration route: Oral
    End date: 2007-06-11

Lipitor
    Dosage: total daily dose: 10 mg unit dose: 10 mg
    Administration route: Oral
    End date: 2007-06-11

Tenormin
    Dosage: total daily dose: 50 mg unit dose: 50 mg
    Administration route: Oral
    End date: 2007-06-11

Pletal
    Administration route: Oral
    End date: 2007-06-11

Bepricor
    Administration route: Oral
    End date: 2007-06-11

Sigmart
    Administration route: Oral
    End date: 2007-06-11

Lendormin
    Administration route: Oral
    Indication: Insomnia
    End date: 2007-06-11

Warfarin Potassium
    Administration route: Oral
    End date: 2007-06-11

Other drugs received by patient: Lasix; Mucosolvan



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

Reported by a consumer/non-health professional from France on 2007-06-20

Patient: 58 year old male, weighing 78.0 kg (171.6 pounds)

Adverse reactions / side effects: Bone Marrow Failure

Adverse event resulted in: life threatening event

Suspect drug(s):
Zantac
    Start date: 2006-09-15
    End date: 2006-09-15

Trandate
    Start date: 2006-09-07
    End date: 2006-09-17

Ciflox
    Dosage: 750mg per day
    Indication: Prostatitis
    Start date: 2006-08-25
    End date: 2006-09-14

Omeprazole
    Start date: 2006-07-05
    End date: 2006-09-12

Vfend
    Start date: 2006-07-27
    End date: 2006-09-11

Valganciclovir HCL
    Start date: 2006-08-16
    End date: 2006-09-11



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