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

DIZZINESS ( 13 FDA reports)
MALAISE ( 10 FDA reports)
VOMITING ( 10 FDA reports)
BLOOD CREATININE INCREASED ( 9 FDA reports)
MUSCULAR WEAKNESS ( 9 FDA reports)
NAUSEA ( 9 FDA reports)
BLOOD UREA INCREASED ( 8 FDA reports)
HEADACHE ( 8 FDA reports)
DECREASED APPETITE ( 7 FDA reports)
PYREXIA ( 7 FDA reports)
RENAL FAILURE ACUTE ( 7 FDA reports)
UPPER RESPIRATORY TRACT INFLAMMATION ( 7 FDA reports)
ABSCESS NECK ( 6 FDA reports)
DYSARTHRIA ( 6 FDA reports)
GASTROENTERITIS ( 6 FDA reports)
HAEMATOCHEZIA ( 6 FDA reports)
INTERSTITIAL LUNG DISEASE ( 6 FDA reports)
LYMPHADENITIS ( 6 FDA reports)
OVARIAN CANCER ( 6 FDA reports)
PHARYNGITIS ( 6 FDA reports)
DRUG INEFFECTIVE ( 5 FDA reports)
ENCEPHALOPATHY ( 5 FDA reports)
ENTEROCOLITIS ( 5 FDA reports)
GAIT DISTURBANCE ( 5 FDA reports)
MENTAL DISORDER ( 5 FDA reports)
NEUROGENIC BLADDER ( 5 FDA reports)
RENAL IMPAIRMENT ( 5 FDA reports)
SPEECH DISORDER ( 5 FDA reports)
URINARY RETENTION ( 5 FDA reports)
CONVULSION ( 4 FDA reports)
FEELING ABNORMAL ( 4 FDA reports)
GAZE PALSY ( 4 FDA reports)
HYPERACUSIS ( 4 FDA reports)
LOSS OF CONSCIOUSNESS ( 4 FDA reports)
NERVE INJURY ( 4 FDA reports)
OVERDOSE ( 4 FDA reports)
RASH ( 4 FDA reports)
SOMNOLENCE ( 4 FDA reports)
ABASIA ( 3 FDA reports)
ABDOMINAL MASS ( 3 FDA reports)
ABDOMINAL PAIN ( 3 FDA reports)
APPENDICITIS ( 3 FDA reports)
DYSPNOEA ( 3 FDA reports)
HEPATIC FUNCTION ABNORMAL ( 3 FDA reports)
INCREASED APPETITE ( 3 FDA reports)
OLIGURIA ( 3 FDA reports)
PRESCRIBED OVERDOSE ( 3 FDA reports)
SCAB ( 3 FDA reports)
AGITATION ( 2 FDA reports)
ANXIETY ( 2 FDA reports)
ASTHENIA ( 2 FDA reports)
BLOOD PRESSURE DIASTOLIC DECREASED ( 2 FDA reports)
BLOOD PRESSURE SYSTOLIC INCREASED ( 2 FDA reports)
C-REACTIVE PROTEIN INCREASED ( 2 FDA reports)
DELIRIUM ( 2 FDA reports)
DIARRHOEA ( 2 FDA reports)
HAEMODIALYSIS ( 2 FDA reports)
HALLUCINATION, VISUAL ( 2 FDA reports)
HYPERREFLEXIA ( 2 FDA reports)
HYPERTENSION ( 2 FDA reports)
IRON DEFICIENCY ( 2 FDA reports)
IRRITABILITY ( 2 FDA reports)
LUNG DISORDER ( 2 FDA reports)
MONOPLEGIA ( 2 FDA reports)
MUSCLE RIGIDITY ( 2 FDA reports)
NERVOUS SYSTEM DISORDER ( 2 FDA reports)
PRURITUS ( 2 FDA reports)
PYODERMA GANGRENOSUM ( 2 FDA reports)
RENAL FAILURE ( 2 FDA reports)
SEROTONIN SYNDROME ( 2 FDA reports)
ABDOMINAL ADHESIONS ( 1 FDA reports)
ADENOCARCINOMA ( 1 FDA reports)
ADHESION ( 1 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 1 FDA reports)
ANAL ABSCESS ( 1 FDA reports)
ANOREXIA ( 1 FDA reports)
ARTHRALGIA ( 1 FDA reports)
ASCITES ( 1 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 1 FDA reports)
BLOOD ALKALINE PHOSPHATASE INCREASED ( 1 FDA reports)
BLOOD LACTATE DEHYDROGENASE INCREASED ( 1 FDA reports)
BLOOD PRESSURE INCREASED ( 1 FDA reports)
BLOOD UREA DECREASED ( 1 FDA reports)
BODY TEMPERATURE INCREASED ( 1 FDA reports)
CELLULITIS ( 1 FDA reports)
CEREBRAL INFARCTION ( 1 FDA reports)
CHOLELITHIASIS ( 1 FDA reports)
DEVICE RELATED INFECTION ( 1 FDA reports)
DIABETIC NEPHROPATHY ( 1 FDA reports)
DIPLOPIA ( 1 FDA reports)
DYSLALIA ( 1 FDA reports)
EYELID OEDEMA ( 1 FDA reports)
FALLOPIAN TUBE CANCER ( 1 FDA reports)
GENERAL PHYSICAL HEALTH DETERIORATION ( 1 FDA reports)
HALLUCINATION, AUDITORY ( 1 FDA reports)
HYPOAESTHESIA ( 1 FDA reports)
HYPOPROTEINAEMIA ( 1 FDA reports)
LIGAMENT RUPTURE ( 1 FDA reports)
MELAENA ( 1 FDA reports)
NEOPLASM ( 1 FDA reports)
OVARIAN EPITHELIAL CANCER ( 1 FDA reports)
PALMAR-PLANTAR ERYTHRODYSAESTHESIA SYNDROME ( 1 FDA reports)
PARAPARESIS ( 1 FDA reports)
PARKINSONISM ( 1 FDA reports)
PLEURAL EFFUSION ( 1 FDA reports)
PNEUMONIA ( 1 FDA reports)
PSEUDOMONAS TEST POSITIVE ( 1 FDA reports)
REFUSAL OF TREATMENT BY PATIENT ( 1 FDA reports)
RESPIRATORY DEPRESSION ( 1 FDA reports)
RESPIRATORY FAILURE ( 1 FDA reports)
SENSORY DISTURBANCE ( 1 FDA reports)
SEPSIS ( 1 FDA reports)
SKIN EROSION ( 1 FDA reports)
TOXIC INDUCED ENCEPHALOPATHY ( 1 FDA reports)
URINARY TRACT INFECTION ( 1 FDA reports)

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