Please choose an event type to view the corresponding MedsFacts report:

PYREXIA ( 16 FDA reports)
VOMITING ( 15 FDA reports)
OEDEMA PERIPHERAL ( 14 FDA reports)
PNEUMOCOCCAL INFECTION ( 14 FDA reports)
PNEUMONIA ASPIRATION ( 14 FDA reports)
SOMNOLENCE ( 14 FDA reports)
URINARY INCONTINENCE ( 14 FDA reports)
CONSTIPATION ( 12 FDA reports)
DRUG ERUPTION ( 11 FDA reports)
DECREASED APPETITE ( 10 FDA reports)
GASTROOESOPHAGEAL REFLUX DISEASE ( 10 FDA reports)
INSOMNIA ( 10 FDA reports)
MALAISE ( 8 FDA reports)
EYE DISCHARGE ( 7 FDA reports)
ANTIBODY TEST POSITIVE ( 6 FDA reports)
OCULAR HYPERAEMIA ( 6 FDA reports)
ORAL INTAKE REDUCED ( 6 FDA reports)
RASH ( 6 FDA reports)
STEVENS-JOHNSON SYNDROME ( 6 FDA reports)
EYELID OEDEMA ( 5 FDA reports)
HEPATIC FUNCTION ABNORMAL ( 5 FDA reports)
LARYNGEAL OEDEMA ( 5 FDA reports)
LIVER DISORDER ( 5 FDA reports)
NEUTROPENIA ( 5 FDA reports)
PNEUMONIA ( 5 FDA reports)
ALTERED STATE OF CONSCIOUSNESS ( 4 FDA reports)
APHTHOUS STOMATITIS ( 4 FDA reports)
DYSTHYMIC DISORDER ( 4 FDA reports)
PNEUMOCYSTIS JIROVECI PNEUMONIA ( 4 FDA reports)
PO2 DECREASED ( 4 FDA reports)
TONGUE NEOPLASM MALIGNANT STAGE UNSPECIFIED ( 4 FDA reports)
URINARY TRACT INFECTION BACTERIAL ( 4 FDA reports)
URINE ANALYSIS ABNORMAL ( 4 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 3 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 3 FDA reports)
BLOOD ALKALINE PHOSPHATASE INCREASED ( 3 FDA reports)
ECZEMA ( 3 FDA reports)
GAMMA-GLUTAMYLTRANSFERASE INCREASED ( 3 FDA reports)
GASTROENTERITIS ( 3 FDA reports)
HALLUCINATION, AUDITORY ( 3 FDA reports)
INFECTIOUS PERITONITIS ( 3 FDA reports)
LARGE INTESTINE CARCINOMA ( 3 FDA reports)
NASOPHARYNGITIS ( 3 FDA reports)
ORAL MUCOSAL ERUPTION ( 3 FDA reports)
OROPHARYNGEAL PAIN ( 3 FDA reports)
PERSECUTORY DELUSION ( 3 FDA reports)
PHARYNGITIS ( 3 FDA reports)
RASH MORBILLIFORM ( 3 FDA reports)
SWELLING FACE ( 3 FDA reports)
ACUTE RESPIRATORY FAILURE ( 2 FDA reports)
ANXIETY ( 2 FDA reports)
BLOOD CHLORIDE DECREASED ( 2 FDA reports)
BLOOD CREATINE PHOSPHOKINASE INCREASED ( 2 FDA reports)
BLOOD SODIUM DECREASED ( 2 FDA reports)
C-REACTIVE PROTEIN INCREASED ( 2 FDA reports)
CARDIAC FAILURE ACUTE ( 2 FDA reports)
CONDITION AGGRAVATED ( 2 FDA reports)
DEPRESSED LEVEL OF CONSCIOUSNESS ( 2 FDA reports)
DISSEMINATED INTRAVASCULAR COAGULATION ( 2 FDA reports)
DRUG LEVEL INCREASED ( 2 FDA reports)
DYSPHONIA ( 2 FDA reports)
DYSPNOEA ( 2 FDA reports)
ELECTROLYTE IMBALANCE ( 2 FDA reports)
ERYTHROPENIA ( 2 FDA reports)
FACE OEDEMA ( 2 FDA reports)
FALL ( 2 FDA reports)
GASTRIC ULCER ( 2 FDA reports)
HAEMATOCRIT DECREASED ( 2 FDA reports)
HAEMOGLOBIN DECREASED ( 2 FDA reports)
HAEMOPTYSIS ( 2 FDA reports)
HEPATITIS ACUTE ( 2 FDA reports)
JUGULAR VEIN DISTENSION ( 2 FDA reports)
LEUKOCYTOCLASTIC VASCULITIS ( 2 FDA reports)
LEUKOPLAKIA ORAL ( 2 FDA reports)
PAIN ( 2 FDA reports)
PHARYNGOLARYNGEAL PAIN ( 2 FDA reports)
PLATELET COUNT DECREASED ( 2 FDA reports)
PLEURAL EFFUSION ( 2 FDA reports)
PORTAL VEIN PHLEBITIS ( 2 FDA reports)
PORTAL VEIN THROMBOSIS ( 2 FDA reports)
RASH GENERALISED ( 2 FDA reports)
RENAL FAILURE ACUTE ( 2 FDA reports)
RENAL TUBULAR NECROSIS ( 2 FDA reports)
SUPRAVENTRICULAR TACHYCARDIA ( 2 FDA reports)
THROMBOSIS ( 2 FDA reports)
UPPER GASTROINTESTINAL HAEMORRHAGE ( 2 FDA reports)
WHITE BLOOD CELL COUNT DECREASED ( 2 FDA reports)
ABASIA ( 1 FDA reports)
ABDOMINAL DISTENSION ( 1 FDA reports)
ACIDOSIS ( 1 FDA reports)
ACTIVATED PARTIAL THROMBOPLASTIN TIME PROLONGED ( 1 FDA reports)
ACUTE RESPIRATORY DISTRESS SYNDROME ( 1 FDA reports)
ANURIA ( 1 FDA reports)
AORTIC VALVE STENOSIS ( 1 FDA reports)
BLOOD LACTATE DEHYDROGENASE INCREASED ( 1 FDA reports)
BLOOD PRESSURE DIASTOLIC DECREASED ( 1 FDA reports)
BLOOD PRESSURE SYSTOLIC DECREASED ( 1 FDA reports)
BLOOD URINE PRESENT ( 1 FDA reports)
CARDIAC ARREST ( 1 FDA reports)
CARDIAC FAILURE ( 1 FDA reports)
CARDIOMEGALY ( 1 FDA reports)
CERVICAL MYELOPATHY ( 1 FDA reports)
CONVULSION ( 1 FDA reports)
COUGH ( 1 FDA reports)
DEPRESSION ( 1 FDA reports)
DIALYSIS ( 1 FDA reports)
DRUG INEFFECTIVE ( 1 FDA reports)
DRUG INTERACTION ( 1 FDA reports)
EOSINOPHIL COUNT INCREASED ( 1 FDA reports)
EPIGLOTTIS ULCER ( 1 FDA reports)
ERYTHEMA MULTIFORME ( 1 FDA reports)
FAECES HARD ( 1 FDA reports)
GASTROENTERITIS VIRAL ( 1 FDA reports)
GASTROINTESTINAL OBSTRUCTION ( 1 FDA reports)
GENERALISED ERYTHEMA ( 1 FDA reports)
HAEMORRHAGE ( 1 FDA reports)
HAEMORRHAGIC DIATHESIS ( 1 FDA reports)
HEART RATE DECREASED ( 1 FDA reports)
HEPATITIS C ( 1 FDA reports)
HYPERLIPIDAEMIA ( 1 FDA reports)
HYPOGLYCAEMIC COMA ( 1 FDA reports)
INCORRECT DOSE ADMINISTERED ( 1 FDA reports)
INTERSTITIAL LUNG DISEASE ( 1 FDA reports)
INTESTINAL HAEMORRHAGE ( 1 FDA reports)
INTESTINAL OBSTRUCTION ( 1 FDA reports)
LARGE INTESTINAL ULCER ( 1 FDA reports)
LARGE INTESTINE PERFORATION ( 1 FDA reports)
LEFT VENTRICULAR FAILURE ( 1 FDA reports)
LYMPHOCYTE STIMULATION TEST POSITIVE ( 1 FDA reports)
MIGRAINE ( 1 FDA reports)
MOUTH ULCERATION ( 1 FDA reports)
MYOCARDIAL ISCHAEMIA ( 1 FDA reports)
NEUROPATHY PERIPHERAL ( 1 FDA reports)
OEDEMA MUCOSAL ( 1 FDA reports)
OSTEOPOROSIS ( 1 FDA reports)
PRURITUS ( 1 FDA reports)
PSYCHOSOCIAL SUPPORT ( 1 FDA reports)
QUADRIPLEGIA ( 1 FDA reports)
RECTAL CANCER ( 1 FDA reports)
RECTAL ULCER HAEMORRHAGE ( 1 FDA reports)
RENAL IMPAIRMENT ( 1 FDA reports)
RESTLESSNESS ( 1 FDA reports)
SCIATICA ( 1 FDA reports)
SKIN TEST POSITIVE ( 1 FDA reports)
SPONDYLITIC MYELOPATHY ( 1 FDA reports)
THROMBOTIC THROMBOCYTOPENIC PURPURA ( 1 FDA reports)
TOXIC SKIN ERUPTION ( 1 FDA reports)
URINE BILIRUBIN DECREASED ( 1 FDA reports)
VISUAL ACUITY REDUCED ( 1 FDA reports)

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