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Index of reports
> Cases resulting in hospitalization (14)
> Cases with Hypersensitivity (2)
Below is the selection of adverse event reports related to Septra (Trimethoprim / Sulfamethoxazole) that includes cases resulting in hospitalization where reactions include hypersensitivity.
Adverse event in receiving Septra (Trimethoprim / Sulfamethoxazole)
Reported by a consumer/non-health professional from United States on 2007-04-05
Patient:
Adverse reactions / side effects: Productive Cough, Blood Bilirubin Increased, Hepatic Failure, Pyrexia, Prothrombin Time Prolonged, Idiosyncratic Drug Reaction, Cardiopulmonary Failure, Blood Creatinine Increased, Blood Alkaline Phosphatase Increased, Metabolic Alkalosis, Hypotension, Blood Lactate Dehydrogenase Increased, Chromaturia, Urine Bilirubin Increased, Hepatocellular Damage, Rash Erythematous, Aspartate Aminotransferase Increased, Rash Maculo-Papular, Jaundice, Hypersensitivity, Skin Exfoliation, Cholestasis, Abdominal Pain Upper, Hepatitis Cholestatic, Fatigue, Hepatomegaly, Gamma-Glutamyltransferase Increased, Thrombocytopenia, Splenomegaly, Oxygen Saturation Decreased, Vomiting, Alanine Aminotransferase Increased, Ascites, Acquired Diaphragmatic Eventration, Hypoalbuminaemia, Lung Infiltration, Leukopenia, RED Blood Cell Sedimentation Rate Increased
Adverse event resulted in: hospitalization
Suspect drug(s):
Septra (Trimethoprim / Sulfamethoxazole)
Adverse event in 34 year old female receiving Septra (Trimethoprim / Sulfamethoxazole)
Reported by a pharmacist from United States on 2007-01-25
Patient: 34 year old female, weighing 54.0 kg (118.8 pounds)
Adverse reactions / side effects: Pharyngeal Oedema, Dyspnoea, Hypersensitivity, Pruritus, Rash
Adverse event resulted in: hospitalization
Suspect drug(s):
Septra (Trimethoprim / Sulfamethoxazole)
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