|
Index of reports
> Cases resulting in other serious reactions (34)
> Cases with Dyspnoea (6)
Below is the selection of adverse event reports related to Zantac (Ranitidine) that includes cases resulting in other serious reactions where reactions include dyspnoea.
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):
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
Tenormin
Administration route: Oral
Indication: Cardiac Failure
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 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):
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
Zantac
Dosage: 50mg 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 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):
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
Zantac
Dosage: 50mg 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 55 year old female receiving Zantac (Ranitidine)
Reported by a pharmacist from Japan on 2007-01-18
Patient: 55 year old female, weighing 57.0 kg (125.4 pounds)
Adverse reactions / side effects: Vomiting, Dyspnoea, Hypersensitivity, Loss of Consciousness, Feeling Cold, Malaise, Depressed Level of Consciousness, Blood Pressure Decreased, Cold Sweat
Suspect drug(s):
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
Zantac
Dosage: 50mg 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 28 year old female receiving Zantac (Ranitidine)
Reported by a physician from Viet NAM on 2007-01-05
Patient: 28 year old female, weighing 65.0 kg (143.0 pounds)
Adverse reactions / side effects: Dyspnoea, Face Oedema, Drug Exposure During Pregnancy, Hypotension, Rash, Laryngeal Oedema
Adverse event resulted in: life threatening event, hospitalization
Suspect drug(s):
Zantac (Ranitidine)
Other drugs received by patient: General Endotracheal Anesthesia
|
