|
Index of reports
> Cases resulting in hospitalization (49)
Below is the selection of adverse event reports related to Zantac (Ranitidine) that includes cases resulting in hospitalization.
Reports 1 - 25 of 49 Next >>
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
Bepricor
Administration route: Oral
End date: 2007-06-11
Lendormin
Administration route: Oral
Indication: Insomnia
End date: 2007-06-11
Lipitor
Dosage: total daily dose: 10 mg unit dose: 10 mg
Administration route: Oral
End date: 2007-06-11
Pletal
Administration route: Oral
End date: 2007-06-11
Sigmart
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
Warfarin Potassium
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
Other drugs received by patient: Lasix; Mucosolvan
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 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 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):
Allopurinol
Dosage: 200 mg/d po
Administration route: Oral
End date: 2006-01-30
Keppra
Dosage: 1000 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
Zantac
Dosage: 150 mg /d po
Administration route: Oral
End date: 2006-01-30
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):
Aspirin
Dosage: daily dose:100mg-freq:day
Administration route: Oral
Start date: 2007-04-27
End date: 2007-06-10
Bepricor
Dosage: daily dose:100mg-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
Lipitor
Dosage: daily dose:10mg
Administration route: Oral
Pletal
Administration route: Oral
Sigmart
Dosage: daily dose:15mg-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
Warfarin Sodium
Dosage: daily dose:.5mg-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
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 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 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
Lorazepam
Start date: 2006-10-01
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
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 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
Bepricor
Administration route: Oral
End date: 2007-06-11
Lendormin
Administration route: Oral
Indication: Insomnia
End date: 2007-06-11
Lipitor
Dosage: total daily dose: 10 mg unit dose: 10 mg
Administration route: Oral
End date: 2007-06-11
Pletal
Administration route: Oral
End date: 2007-06-11
Sigmart
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
Warfarin Potassium
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
Other drugs received by patient: Lasix; Mucosolvan
Adverse event in 20 year old female receiving Zantac (Ranitidine)
Reported by a consumer/non-health professional from France on 2007-05-31
Patient: 20 year old female
Adverse reactions / side effects: Aplastic Anaemia, Neutropenia, Normochromic Normocytic Anaemia
Adverse event resulted in: hospitalization
Suspect drug(s):
Effexor
Administration route: Oral
End date: 2007-02-15
Rubozinc
Start date: 2007-02-23
Zantac
Administration route: Oral
Start date: 2007-01-11
End date: 2007-02-01
Other drugs received by patient: Atarax; Calcium Carbonate + Cholecalciferol; Phocytan; Vitamin B1 B6; Diffu-K; Imodium; Tiorfan; Heptamyl; Lovenox; Multivitamin; Phosphoneuros; Cernevit-12; Unknown Drug; Ethinyl Estradiol and Levonorgestrel; Unknown OTC
Adverse event in female receiving Zantac (Ranitidine)
Reported by a physician from Japan on 2007-05-22
Patient: female, weighing 48.0 kg (105.6 pounds)
Adverse reactions / side effects: Vomiting, Diarrhoea, Delirium
Adverse event resulted in: hospitalization
Suspect drug(s):
Alfarol
Dosage: 1 rg
Administration route: Oral
Indication: Rheumatoid Arthritis
Iscotin
Dosage: 1 rg
Administration route: Oral
Indication: Infection Prophylaxis
Loxonin
Administration route: Oral
Indication: Rheumatoid Arthritis
Predonine
Indication: Rheumatoid Arthritis
Remicade
Remicade
Remicade
Remicade
Remicade
Remicade
Indication: Rheumatoid Arthritis
Rheumatrex
Administration route: Oral
Indication: Rheumatoid Arthritis
Selbex
Dosage: 1 rg
Administration route: Oral
Indication: Prophylaxis
Solanax
Dosage: 1 rg
Administration route: Oral
Indication: Insomnia
Zantac
Dosage: 1 rg
Administration route: Oral
Indication: Prophylaxis
Adverse event in 7 month old female receiving Zantac (Ranitidine)
Reported by a pharmacist from Canada on 2007-05-10
Patient: 7 month old female, weighing 5.0 kg (11.0 pounds)
Adverse reactions / side effects: Overdose, Medication Error, Adverse Event, Hydrocephalus
Adverse event resulted in: hospitalization
Suspect drug(s):
Zantac (Ranitidine)
Adverse event in 13 year old female receiving Zantac (Ranitidine)
Reported by a pharmacist from United States on 2007-05-09
Patient: 13 year old female
Adverse reactions / side effects: Agitation, Obsessive-Compulsive Disorder, Accidental Overdose, Thought Insertion, Feeling of Despair, Blood Lactate Dehydrogenase Increased, Tremor, Irritability, Post-Traumatic Stress Disorder, Aspartate Aminotransferase Increased, Suicide Attempt, Major Depression, Disturbance in Attention, Drug Screen Positive, Feeling Guilty, Mental Status Changes, Somnolence, Pallor, Sinus Bradycardia, Poor Quality Sleep, Dizziness, Anger, Multiple Drug Overdose, Flashback, Tearfulness, Lethargy, Vomiting, Nausea, Alanine Aminotransferase Increased, Trichotillomania, Amnesia, Arrhythmia, Hepatic Enzyme Increased, Anxiety, Syncope, Asthenia
Adverse event resulted in: hospitalization
Suspect drug(s):
Corgard
Dosage: 1tab single dose
Administration route: Oral
Start date: 2001-02-07
End date: 2001-02-07
Paxil
Dosage: 10mg per day
Administration route: Oral
Indication: Anxiety
Start date: 1998-01-01
End date: 2003-01-01
Pravachol
Administration route: Oral
Start date: 2001-02-07
End date: 2001-02-07
Tenex
Dosage: 2mg twice per day
Administration route: Oral
Tylenol
Dosage: 1bt single dose
Administration route: Oral
Start date: 2001-02-07
End date: 2001-02-07
Zantac
Dosage: 8tab single dose
Administration route: Oral
Start date: 2007-02-01
End date: 2007-02-01
Zoloft
Dosage: 15tab single dose
Administration route: Oral
Start date: 2001-02-07
End date: 2001-02-07
Other drugs received by patient: Ortho TRI-Cyclen; Clonidine; Albuterol
Adverse event in 13 year old female receiving Zantac (Ranitidine)
Reported by a pharmacist from United States on 2007-05-02
Patient: 13 year old female
Adverse reactions / side effects: Mental Status Changes, Pallor, Somnolence, Sinus Bradycardia, Poor Quality Sleep, Thought Insertion, Anger, Dizziness, Multiple Drug Overdose, Tearfulness, Lethargy, Feeling of Despair, Vomiting, Nausea, Trichotillomania, Amnesia, Hepatic Enzyme Increased, Tremor, Arrhythmia, Anxiety, Irritability, Post-Traumatic Stress Disorder, Syncope, Suicide Attempt, Major Depression, Disturbance in Attention, Asthenia
Adverse event resulted in: hospitalization
Suspect drug(s):
Corgard
Dosage: 1tab single dose
Administration route: Oral
Start date: 2001-02-07
End date: 2001-02-07
Paxil
Dosage: 10mg per day
Administration route: Oral
Indication: Anxiety
Start date: 1998-01-01
End date: 2003-01-01
Pravachol
Administration route: Oral
Start date: 2001-02-07
End date: 2001-02-07
Tenex
Dosage: 2mg twice per day
Administration route: Oral
Tylenol
Dosage: 1bt single dose
Administration route: Oral
Start date: 2001-02-07
End date: 2001-02-07
Zantac
Dosage: 8tab single dose
Administration route: Oral
Start date: 2007-02-01
End date: 2007-02-01
Zoloft
Dosage: 15tab single dose
Administration route: Oral
Start date: 2001-02-07
End date: 2001-02-07
Other drugs received by patient: Ortho TRI-Cyclen; Clonidine; Albuterol
Adverse event in 77 year old female receiving Zantac (Ranitidine)
Reported by a physician from Japan on 2007-05-02
Patient: 77 year old female, weighing 45.0 kg (99.0 pounds)
Adverse reactions / side effects: Rhabdomyolysis, Dysstasia, Convulsions Local, Hypoaesthesia
Adverse event resulted in: life threatening event, hospitalization
Suspect drug(s):
Zantac (Ranitidine)
Other drugs received by patient: Cyanocobalamin; Vitamedin; Mucosta
Adverse event in 48 year old female receiving Zantac (Ranitidine)
Reported by a consumer/non-health professional from France on 2007-04-26
Patient: 48 year old female, weighing 63.0 kg (138.6 pounds)
Adverse reactions / side effects: Nausea, Anaphylactic Shock, Skin Test Positive, Sense of Oppression, Loss of Consciousness, Generalised Erythema, Face Oedema, Cyanosis, Respiratory Arrest, Blood Pressure Decreased
Adverse event resulted in: life threatening event, hospitalization
Suspect drug(s):
Polaramine
Start date: 2006-08-16
End date: 2006-08-16
Polaramine
Dosage: 1unit single dose
Start date: 2006-09-13
End date: 2006-09-13
Zantac
Start date: 2006-08-16
End date: 2006-08-16
Zantac
Dosage: 1unit single dose
Start date: 2006-09-13
End date: 2006-09-13
Adverse event in 73 year old male receiving Zantac (Ranitidine)
Reported by a physician from Japan on 2007-04-25
Patient: 73 year old male
Adverse reactions / side effects: Cholecystitis Acute, Duodenal Ulcer Haemorrhage, Cholestasis, Lymphocyte Stimulation Test Positive, Arrhythmia, Liver Disorder
Adverse event resulted in: life threatening event, hospitalization
Suspect drug(s):
Pepcid RPD
Administration route: Oral
Indication: Duodenal Ulcer
Start date: 2006-12-17
End date: 2007-02-12
Promac
Administration route: Oral
Indication: Duodenal Ulcer
Start date: 2006-10-22
End date: 2007-02-15
Zantac
Indication: Cholecystitis
Start date: 2007-02-15
End date: 2007-02-21
Other drugs received by patient: Cefoperazone Sodium and Sulbactam Sodium; Allopurinol; Norvasc; Flivas
Adverse event in 13 year old female receiving Zantac (Ranitidine)
Reported by a pharmacist from United States on 2007-04-23
Patient: 13 year old female
Adverse reactions / side effects: Mental Status Changes, Somnolence, Pallor, Sinus Bradycardia, Poor Quality Sleep, Thought Insertion, Anger, Multiple Drug Overdose, Tearfulness, Lethargy, Feeling of Despair, Vomiting, Nausea, Trichotillomania, Tremor, Arrhythmia, Hepatic Enzyme Increased, Anxiety, Irritability, Post-Traumatic Stress Disorder, Major Depression, Suicide Attempt, Asthenia
Adverse event resulted in: hospitalization
Suspect drug(s):
Corgard
Dosage: 1tab single dose
Administration route: Oral
Start date: 2001-02-07
End date: 2001-02-07
Paxil
Dosage: 10mg per day
Administration route: Oral
Indication: Anxiety
Start date: 1998-01-01
End date: 2003-01-01
Pravachol
Administration route: Oral
Start date: 2001-02-07
End date: 2001-02-07
Tenex
Dosage: 2mg twice per day
Administration route: Oral
Tylenol
Dosage: 1bt single dose
Administration route: Oral
Start date: 2001-02-07
End date: 2001-02-07
Zantac
Dosage: 8tab single dose
Administration route: Oral
Start date: 2007-02-01
End date: 2007-02-01
Zoloft
Dosage: 15tab single dose
Administration route: Oral
Start date: 2001-02-07
End date: 2001-02-07
Other drugs received by patient: Ortho TRI-Cyclen; Clonidine
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):
Polaramine
Dosage: 2.5mg single dose
Start date: 2007-03-09
End date: 2007-03-09
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
Other drugs received by patient: Polaramine; Taxol; Herceptin; Carboplatin; Solu-Medrol
Adverse event in 73 year old male receiving Zantac (Ranitidine)
Reported by a physician from Japan on 2007-04-19
Patient: 73 year old male
Adverse reactions / side effects: Liver Disorder
Adverse event resulted in: life threatening event, hospitalization
Suspect drug(s):
Pepcid RPD
Administration route: Oral
Indication: Duodenal Ulcer
Start date: 2006-12-17
End date: 2007-02-12
Promac
Administration route: Oral
Indication: Duodenal Ulcer
Zantac
Indication: Cholecystitis
Start date: 2007-02-15
End date: 2007-02-21
Other drugs received by patient: Cefoperazone Sodium and Sulbactam Sodium; Allopurinol; Norvasc; Flivas
Adverse event in 13 year old female receiving Zantac (Ranitidine)
Reported by a pharmacist from United States on 2007-04-17
Patient: 13 year old female
Adverse reactions / side effects: Mental Status Changes, Somnolence, Pallor, Sinus Bradycardia, Poor Quality Sleep, Thought Insertion, Anger, Multiple Drug Overdose, Tearfulness, Lethargy, Feeling of Despair, Vomiting, Nausea, Hepatic Enzyme Increased, Arrhythmia, Anxiety, Irritability, Post-Traumatic Stress Disorder, Major Depression, Suicide Attempt
Adverse event resulted in: hospitalization
Suspect drug(s):
Corgard
Dosage: 1tab single dose
Administration route: Oral
Start date: 2001-02-07
End date: 2001-02-07
Paxil
Dosage: 10mg per day
Administration route: Oral
Indication: Anxiety
Start date: 1998-01-01
End date: 2003-01-01
Pravachol
Administration route: Oral
Start date: 2001-02-07
End date: 2001-02-07
Tenex
Dosage: 2mg twice per day
Administration route: Oral
Tylenol
Dosage: 1bt single dose
Administration route: Oral
Start date: 2001-02-07
End date: 2001-02-07
Zantac
Dosage: 8tab single dose
Administration route: Oral
Start date: 2007-02-01
End date: 2007-02-01
Zoloft
Dosage: 15tab single dose
Administration route: Oral
Start date: 2001-02-07
End date: 2001-02-07
Other drugs received by patient: Ortho TRI-Cyclen
Page 1 Next >>
|
