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Index of reports
> Cases resulting in other serious reactions (34)
Below is the selection of adverse event reports related to Zantac (Ranitidine) that includes cases resulting in other serious reactions.
Reports 1 - 25 of 34 Next >>
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 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 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 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 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 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 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 2007-06-28
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 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 female receiving Zantac (Ranitidine)
Reported by a consumer/non-health professional from United States on 2007-05-29
Patient: female, weighing 22.7 kg (49.9 pounds)
Adverse reactions / side effects: Dermatitis
Suspect drug(s):
Vistaril (Oral Susp)
Indication: Hypersensitivity
Zyrtec
Indication: Hypersensitivity
Fluconazole
Zyvox Suspension, Oral
Indication: Staphylococcal Infection
Start date: 2007-05-01
End date: 2007-05-20
Amlodipine
Acyclovir
Calcium Chloride
Creon
Daclizumab
Enalapril Maleate
Hydramine
Levaquin
Start date: 2007-01-01
End date: 2007-05-01
Mupirocin
Neutra-Phos
Orapred
Pentamidine Isethionate
Prednisone TAB
Prevacid
Protopic
ALL Other Therapeutic Products
Vitamin D
Zantac
Flintstones Multiple Vitamins
Cyclosporine
Magnesium Sulfate
Adverse event in 28 year old female receiving Zantac (Ranitidine)
Reported by a consumer/non-health professional from United States on 2007-05-09
Patient: 28 year old female, weighing 81.6 kg (179.5 pounds)
Adverse reactions / side effects: Facial Pain, Thyroxine Increased, Drug Toxicity, Urticaria Generalised, TRI-Iodothyronine Increased, Panic Attack, Vision Blurred, Anticholinergic Syndrome
Suspect drug(s):
Yasmin
Dosage: 1 tab(s), 1x/day
Administration route: Oral
Indication: Oral Contraception
Start date: 2001-01-01
End date: 2007-03-03
Benadryl ^warner-Lambert^ / USA /
Clarinex / USA /
Allegra
Hydroxyzine
Zantac
Singulair
Dosage: unk, 1x/day
Administration route: Oral
Start date: 2007-02-12
Other drugs received by patient: Daypro; Naproxen
Adverse event in 33 year old receiving Zantac (Ranitidine)
Reported by a consumer/non-health professional from United Kingdom on 2007-05-04
Patient: 33 year old
Adverse reactions / side effects: Periorbital Oedema, Flushing, Face Oedema, Hypotension
Suspect drug(s):
Zantac (Ranitidine)
Adverse event in 35 year old female receiving Zantac (Ranitidine)
Reported by a consumer/non-health professional from United Kingdom on 2007-04-23
Patient: 35 year old female
Adverse reactions / side effects: Hypersensitivity, Mydriasis, Pharyngeal Oedema, Miosis, Aphasia, Vision Blurred, Oxygen Saturation Decreased, Laryngospasm
Adverse event resulted in: life threatening event
Suspect drug(s):
Zantac (Ranitidine)
Other drugs received by patient: Cefuroxime; Cyclizine; Metronidazole; Ondansetron; Paracetamol; Tinzaparin; Paracetamol
Adverse event in 55 year old female receiving Zantac (Ranitidine)
Reported by a pharmacist from Japan on 2007-04-23
Patient: 55 year old female, weighing 57.0 kg (125.4 pounds)
Adverse reactions / side effects: Vomiting, Hypersensitivity, Dyspnoea, Feeling Cold, Loss of Consciousness, Malaise, Depressed Level of Consciousness, Blood Pressure Decreased, Cold Sweat, Shock
Suspect drug(s):
Zantac
Dosage: 50mg per day
Indication: Premedication
Start date: 2006-12-11
End date: 2006-12-11
Decadron
Dosage: 20mg per day
Indication: Premedication
Start date: 2006-12-11
End date: 2006-12-11
Kytril
Dosage: 3mg per day
Indication: Premedication
Start date: 2006-12-11
End date: 2006-12-11
Other drugs received by patient: Unknown Medication; Pursennid; Magnesium Oxide; Flomox; Solantal; Slow-FE; Seishoku; Restamin; Paclitaxel; Pirarubicin Hydrochloride; Carboplatin
Adverse event in 70 year old male receiving Zantac (Ranitidine)
Reported by a pharmacist from Japan on 2007-04-13
Patient: 70 year old male
Adverse reactions / side effects: Diarrhoea, Deafness, Constipation
Suspect drug(s):
Zantac (Ranitidine)
Adverse event in 79 year old male receiving Zantac (Ranitidine)
Reported by a pharmacist from Japan on 2007-04-12
Patient: 79 year old male
Adverse reactions / side effects: Idiopathic Thrombocytopenic Purpura
Suspect drug(s):
Zantac (Ranitidine)
Adverse event in 28 year old female receiving Zantac (Ranitidine)
Reported by a consumer/non-health professional from United States on 2007-03-27
Patient: 28 year old female, weighing 81.6 kg (179.5 pounds)
Adverse reactions / side effects: Urticaria Generalised, Anticholinergic Syndrome, Facial Pain
Suspect drug(s):
Yasmin
Dosage: 1 tab(s), 1x/day
Administration route: Oral
Indication: Oral Contraception
Start date: 2001-01-01
End date: 2007-03-03
Benadryl ^warner-Lambert^ / USA /
Clarinex / USA /
Allegra
Hydroxyzine
Zantac
Adverse event in male receiving Zantac (Ranitidine)
Reported by a health professional (non-physician/pharmacist) from United States on 2007-03-22
Patient: male, weighing 4.8 kg (10.6 pounds)
Adverse reactions / side effects: Bacteria Stool Identified, Mucous Stools, Pyrexia, Thirst, Eructation, Faeces Discoloured, Abdominal Discomfort, Overdose, Frequent Bowel Movements, Medication Error, Alanine Aminotransferase Increased, Stomach Discomfort, Discomfort, Haematochezia, Diarrhoea, Throat Irritation, Aspartate Aminotransferase Increased, Pollakiuria
Suspect drug(s):
Zantac
Administration route: Oral
Start date: 2006-12-02
End date: 2007-02-09
Prilosec
Dosage: 10mg single dose
Indication: Drug USE FOR Unknown Indication
Start date: 2006-12-10
End date: 2006-12-10
Other drugs received by patient: Acidophilus; Bifidus
Adverse event in 33 year old female receiving Zantac (Ranitidine)
Reported by a consumer/non-health professional from Norway on 2007-03-22
Patient: 33 year old female
Adverse reactions / side effects: Benign Intracranial Hypertension
Suspect drug(s):
Zantac (Ranitidine)
Adverse event in 35 year old female receiving Zantac (Ranitidine)
Reported by a pharmacist from United Kingdom on 2007-03-20
Patient: 35 year old female
Adverse reactions / side effects: Mydriasis, Hypersensitivity, Aphasia, Pharyngeal Oedema, Miosis, Vision Blurred, Pharmaceutical Product Complaint, Laryngospasm, Oxygen Saturation Decreased
Adverse event resulted in: life threatening event
Suspect drug(s):
Zantac (Ranitidine)
Adverse event in 5 month old male receiving Zantac (Ranitidine)
Reported by a consumer/non-health professional from United States on 2007-03-07
Patient: 5 month old male, weighing 4.8 kg (10.6 pounds)
Adverse reactions / side effects: Bacteria Stool Identified, Alanine Aminotransferase Increased, Stomach Discomfort, Mucous Stools, Pyrexia, Thirst, Discomfort, Eructation, Faeces Discoloured, Haematochezia, Frequent Bowel Movements, Overdose, Throat Irritation, Diarrhoea, Medication Error, Aspartate Aminotransferase Increased, Pollakiuria
Suspect drug(s):
Zantac
Administration route: Oral
Start date: 2006-12-02
End date: 2007-02-16
Prilosec
Indication: Drug USE FOR Unknown Indication
Other drugs received by patient: Acidophilus; Bifidus
Adverse event in 12 year old female receiving Zantac (Ranitidine)
Reported by a consumer/non-health professional from United States on 2007-02-20
Patient: 12 year old female
Adverse reactions / side effects: Colour Blindness, Dizziness, Blindness, Loss of Consciousness
Suspect drug(s):
Zantac
Dosage: 150mg per day
Administration route: Oral
Indication: Gastrooesophageal Reflux Disease
Start date: 2006-05-22
End date: 2006-06-08
Prevacid
Dosage: 30mg per day
Start date: 2006-05-22
End date: 2006-06-08
Other drugs received by patient: NO Concurrent Medication
Adverse event in 30 year old female receiving Zantac (Ranitidine)
Reported by a pharmacist from United Kingdom on 2007-02-20
Patient: 30 year old female
Adverse reactions / side effects: Anaphylactic Reaction
Adverse event resulted in: life threatening event
Suspect drug(s):
Maxolon
Dosage: 10 mg, intravenous
Start date: 2006-05-01
Zantac
Dosage: 50 mg, qd, intravenous
Start date: 2006-05-01
Zantac
Dosage: 50 mg, qdm, intravenous
Indication: Premedication
Start date: 2006-05-15
End date: 2006-05-15
Other drugs received by patient: Metoclopramide
Adverse event in 69 year old female receiving Zantac (Ranitidine)
Reported by a pharmacist from Japan on 2007-02-14
Patient: 69 year old female, weighing 45.0 kg (99.0 pounds)
Adverse reactions / side effects: Hot Flush, Nausea, Painful Respiration, Shock, Loss of Consciousness
Suspect drug(s):
Zantac (Ranitidine)
Other drugs received by patient: Serotone; Decadron; Taxol; Herceptin
Adverse event in 55 year old female receiving Zantac (Ranitidine)
Reported by a pharmacist from Japan on 2007-02-09
Patient: 55 year old female, weighing 57.0 kg (125.4 pounds)
Adverse reactions / side effects: Vomiting, Hypersensitivity, Dyspnoea, Feeling Cold, Loss of Consciousness, Malaise, Depressed Level of Consciousness, Blood Pressure Decreased, Cold Sweat, Shock
Suspect drug(s):
Zantac
Dosage: 50mg per day
Indication: Premedication
Start date: 2006-12-11
End date: 2006-12-11
Decadron
Dosage: 20mg per day
Indication: Premedication
Start date: 2006-12-11
End date: 2006-12-11
Kytril
Dosage: 3mg per day
Indication: Premedication
Start date: 2006-12-11
End date: 2006-12-11
Other drugs received by patient: Unknown Medication; Pursennid; Magnesium Oxide; Flomox; Solantal; Slow-FE; Seishoku; Restamin; Paclitaxel; Pirarubicin Hydrochloride; Carboplatin
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