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DYSPNOEA ( 6 FDA reports)
GENERAL PHYSICAL HEALTH DETERIORATION ( 6 FDA reports)
MYELODYSPLASTIC SYNDROME ( 5 FDA reports)
WEIGHT INCREASED ( 5 FDA reports)
CONFUSIONAL STATE ( 4 FDA reports)
PNEUMONIA ( 4 FDA reports)
AMENORRHOEA ( 3 FDA reports)
DIARRHOEA ( 3 FDA reports)
DIZZINESS ( 3 FDA reports)
INCORRECT DOSE ADMINISTERED ( 3 FDA reports)
MALAISE ( 3 FDA reports)
MENSTRUATION IRREGULAR ( 3 FDA reports)
OEDEMA PERIPHERAL ( 3 FDA reports)
PYREXIA ( 3 FDA reports)
TREMOR ( 3 FDA reports)
ABDOMINAL PAIN ( 2 FDA reports)
ACUTE GENERALISED EXANTHEMATOUS PUSTULOSIS ( 2 FDA reports)
AGGRESSION ( 2 FDA reports)
AGITATION ( 2 FDA reports)
ASTHENIA ( 2 FDA reports)
ASTHMA ( 2 FDA reports)
BRONCHOPNEUMONIA ( 2 FDA reports)
CHEST PAIN ( 2 FDA reports)
DROP ATTACKS ( 2 FDA reports)
DYSARTHRIA ( 2 FDA reports)
DYSPEPSIA ( 2 FDA reports)
FEELING HOT ( 2 FDA reports)
GAIT DISTURBANCE ( 2 FDA reports)
GRAVITATIONAL OEDEMA ( 2 FDA reports)
HEADACHE ( 2 FDA reports)
HYPERTENSION ( 2 FDA reports)
HYPOTENSION ( 2 FDA reports)
INAPPROPRIATE SCHEDULE OF DRUG ADMINISTRATION ( 2 FDA reports)
INFECTION ( 2 FDA reports)
LOWER EXTREMITY MASS ( 2 FDA reports)
MENTAL IMPAIRMENT ( 2 FDA reports)
MYALGIA ( 2 FDA reports)
NAUSEA ( 2 FDA reports)
OFF LABEL USE ( 2 FDA reports)
OXYGEN SATURATION DECREASED ( 2 FDA reports)
PNEUMOCOCCAL SEPSIS ( 2 FDA reports)
PROTEINURIA ( 2 FDA reports)
PRURITUS ( 2 FDA reports)
PSYCHOMOTOR SKILLS IMPAIRED ( 2 FDA reports)
SOMNOLENCE ( 2 FDA reports)
SOPOR ( 2 FDA reports)
SUBARACHNOID HAEMORRHAGE ( 2 FDA reports)
VISION BLURRED ( 2 FDA reports)
VOMITING ( 2 FDA reports)
WOUND ( 2 FDA reports)
ABDOMINAL DISTENSION ( 1 FDA reports)
AMNESIA ( 1 FDA reports)
ARRHYTHMIA SUPRAVENTRICULAR ( 1 FDA reports)
ARTHRALGIA ( 1 FDA reports)
BLADDER DILATATION ( 1 FDA reports)
BLINDNESS ( 1 FDA reports)
BLOOD PRESSURE INCREASED ( 1 FDA reports)
BLOOD SODIUM ABNORMAL ( 1 FDA reports)
BRONCHIAL HYPERREACTIVITY ( 1 FDA reports)
CAPSULE ISSUE ( 1 FDA reports)
CARDIAC DISCOMFORT ( 1 FDA reports)
CARDIAC VALVE DISEASE ( 1 FDA reports)
CELLULITIS ( 1 FDA reports)
CEREBRAL ISCHAEMIA ( 1 FDA reports)
CEREBROVASCULAR ACCIDENT ( 1 FDA reports)
CONVULSION ( 1 FDA reports)
COUGH ( 1 FDA reports)
DECREASED APPETITE ( 1 FDA reports)
DENGUE FEVER ( 1 FDA reports)
DIABETES MELLITUS ( 1 FDA reports)
DRUG INTERACTION ( 1 FDA reports)
EUPHORIC MOOD ( 1 FDA reports)
FATIGUE ( 1 FDA reports)
GALLBLADDER PERFORATION ( 1 FDA reports)
GASTRIC DILATATION ( 1 FDA reports)
HELICOBACTER PYLORI IDENTIFICATION TEST POSITIVE ( 1 FDA reports)
HEPATIC PAIN ( 1 FDA reports)
HYPERHIDROSIS ( 1 FDA reports)
HYPOAESTHESIA ( 1 FDA reports)
HYPONATRAEMIA ( 1 FDA reports)
INFLUENZA LIKE ILLNESS ( 1 FDA reports)
IRON DEFICIENCY ANAEMIA ( 1 FDA reports)
MENINGITIS ( 1 FDA reports)
MENINGITIS PNEUMOCOCCAL ( 1 FDA reports)
MICTURITION URGENCY ( 1 FDA reports)
NERVOUS SYSTEM DISORDER ( 1 FDA reports)
NERVOUSNESS ( 1 FDA reports)
ORAL NEOPLASM BENIGN ( 1 FDA reports)
OVERDOSE ( 1 FDA reports)
PAIN IN EXTREMITY ( 1 FDA reports)
PALPITATIONS ( 1 FDA reports)
PHARYNGEAL OEDEMA ( 1 FDA reports)
PLATELET COUNT ABNORMAL ( 1 FDA reports)
POLYURIA ( 1 FDA reports)
PRODUCT QUALITY ISSUE ( 1 FDA reports)
PROSTHESIS IMPLANTATION ( 1 FDA reports)
SOMNAMBULISM ( 1 FDA reports)
SPEECH DISORDER ( 1 FDA reports)
SUICIDE ATTEMPT ( 1 FDA reports)
TACHYCARDIA ( 1 FDA reports)
THROAT TIGHTNESS ( 1 FDA reports)
THROMBOCYTOPENIA ( 1 FDA reports)
THROMBOSIS ( 1 FDA reports)
URINARY TRACT INFECTION ( 1 FDA reports)
VASCULAR GRAFT ( 1 FDA reports)

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