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

NAUSEA ( 21 FDA reports)
PERIPHERAL SENSORY NEUROPATHY ( 14 FDA reports)
PSYCHOTIC DISORDER ( 13 FDA reports)
FATIGUE ( 11 FDA reports)
BLOOD PRESSURE INCREASED ( 10 FDA reports)
CONFUSIONAL STATE ( 10 FDA reports)
NEUTROPENIA ( 9 FDA reports)
VOMITING ( 9 FDA reports)
DEATH ( 8 FDA reports)
DRUG TOXICITY ( 8 FDA reports)
BLOOD ALKALINE PHOSPHATASE INCREASED ( 7 FDA reports)
DIARRHOEA ( 7 FDA reports)
DRUG EXPOSURE DURING PREGNANCY ( 7 FDA reports)
DYSPNOEA ( 7 FDA reports)
HALLUCINATION ( 7 FDA reports)
MYALGIA ( 7 FDA reports)
PYREXIA ( 7 FDA reports)
THROMBOCYTOPENIA ( 7 FDA reports)
WEIGHT DECREASED ( 7 FDA reports)
AGGRESSION ( 6 FDA reports)
AGITATION ( 6 FDA reports)
CARDIAC MURMUR ( 6 FDA reports)
DECREASED APPETITE ( 6 FDA reports)
DYSGEUSIA ( 6 FDA reports)
INSOMNIA ( 6 FDA reports)
NEUTROPENIC INFECTION ( 6 FDA reports)
NEUTROPHIL COUNT INCREASED ( 6 FDA reports)
ASTHENIA ( 5 FDA reports)
DEHYDRATION ( 5 FDA reports)
DEPRESSION ( 5 FDA reports)
ERYTHEMA ( 5 FDA reports)
LOSS OF CONSCIOUSNESS ( 5 FDA reports)
RASH ( 5 FDA reports)
VENTRICULAR SEPTAL DEFECT ( 5 FDA reports)
BACK PAIN ( 4 FDA reports)
CONGENITAL ANOMALY ( 4 FDA reports)
DRY SKIN ( 4 FDA reports)
DYSARTHRIA ( 4 FDA reports)
EPISTAXIS ( 4 FDA reports)
HEADACHE ( 4 FDA reports)
INFECTION ( 4 FDA reports)
LETHARGY ( 4 FDA reports)
MOOD ALTERED ( 4 FDA reports)
PERICARDITIS ( 4 FDA reports)
SEDATION ( 4 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 3 FDA reports)
ALOPECIA ( 3 FDA reports)
ANGINA PECTORIS ( 3 FDA reports)
ANOREXIA ( 3 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 3 FDA reports)
BASEDOW'S DISEASE ( 3 FDA reports)
BLOOD POTASSIUM DECREASED ( 3 FDA reports)
BLOOD THYROID STIMULATING HORMONE DECREASED ( 3 FDA reports)
BLOOD THYROID STIMULATING HORMONE INCREASED ( 3 FDA reports)
BREAST DISCHARGE ( 3 FDA reports)
BREAST INJURY ( 3 FDA reports)
BREAST PAIN ( 3 FDA reports)
BRONCHITIS ( 3 FDA reports)
C-REACTIVE PROTEIN INCREASED ( 3 FDA reports)
CONSTIPATION ( 3 FDA reports)
CONTUSION ( 3 FDA reports)
COORDINATION ABNORMAL ( 3 FDA reports)
COUGH ( 3 FDA reports)
DRY EYE ( 3 FDA reports)
DYSPHONIA ( 3 FDA reports)
FEELING ABNORMAL ( 3 FDA reports)
GASTROINTESTINAL TOXICITY ( 3 FDA reports)
GINGIVAL BLEEDING ( 3 FDA reports)
HAEMATOCHEZIA ( 3 FDA reports)
HEART RATE INCREASED ( 3 FDA reports)
HYPERTHYROIDISM ( 3 FDA reports)
HYPOTHYROIDISM ( 3 FDA reports)
INFLUENZA ( 3 FDA reports)
INFUSION RELATED REACTION ( 3 FDA reports)
INTERNATIONAL NORMALISED RATIO DECREASED ( 3 FDA reports)
LARYNGITIS ( 3 FDA reports)
MENSTRUAL DISORDER ( 3 FDA reports)
MOOD SWINGS ( 3 FDA reports)
NASAL CONGESTION ( 3 FDA reports)
OVERDOSE ( 3 FDA reports)
PAIN ( 3 FDA reports)
RED BLOOD CELL SEDIMENTATION RATE INCREASED ( 3 FDA reports)
SEPSIS ( 3 FDA reports)
SUDDEN CARDIAC DEATH ( 3 FDA reports)
THROAT IRRITATION ( 3 FDA reports)
TINEA INFECTION ( 3 FDA reports)
TONSILLITIS ( 3 FDA reports)
URTICARIA ( 3 FDA reports)
WEIGHT INCREASED ( 3 FDA reports)
WHITE BLOOD CELL COUNT DECREASED ( 3 FDA reports)
ABDOMINAL PAIN UPPER ( 2 FDA reports)
ANAEMIA ( 2 FDA reports)
BRADYCARDIA ( 2 FDA reports)
CARDIAC ARREST ( 2 FDA reports)
CARDIAC FAILURE CONGESTIVE ( 2 FDA reports)
CARDIOVASCULAR INSUFFICIENCY ( 2 FDA reports)
DEEP VEIN THROMBOSIS ( 2 FDA reports)
DYSGRAPHIA ( 2 FDA reports)
EMBOLISM ( 2 FDA reports)
FALL ( 2 FDA reports)
HYPERTENSION ( 2 FDA reports)
HYPOTENSION ( 2 FDA reports)
LEUKOPENIA ( 2 FDA reports)
LUNG INFILTRATION ( 2 FDA reports)
LYMPHOPENIA ( 2 FDA reports)
MALIGNANT NEOPLASM PROGRESSION ( 2 FDA reports)
METASTASES TO LUNG ( 2 FDA reports)
OCULAR HYPERAEMIA ( 2 FDA reports)
OEDEMA PERIPHERAL ( 2 FDA reports)
OFF LABEL USE ( 2 FDA reports)
PAIN IN EXTREMITY ( 2 FDA reports)
PANCREATITIS ( 2 FDA reports)
PERFORMANCE STATUS DECREASED ( 2 FDA reports)
RESPIRATORY DEPRESSION ( 2 FDA reports)
SUBSTANCE ABUSE ( 2 FDA reports)
SUICIDE ATTEMPT ( 2 FDA reports)
THROMBOCYTHAEMIA ( 2 FDA reports)
UPPER RESPIRATORY TRACT INFECTION ( 2 FDA reports)
ABDOMINAL DISCOMFORT ( 1 FDA reports)
ABDOMINAL DISTENSION ( 1 FDA reports)
ABDOMINAL PAIN ( 1 FDA reports)
ACCIDENTAL DEATH ( 1 FDA reports)
ACCIDENTAL POISONING ( 1 FDA reports)
AMNESIA ( 1 FDA reports)
ANXIETY ( 1 FDA reports)
ARTERIAL OCCLUSIVE DISEASE ( 1 FDA reports)
ATRIAL SEPTAL DEFECT ( 1 FDA reports)
BALANCE DISORDER ( 1 FDA reports)
BILIRUBIN CONJUGATED INCREASED ( 1 FDA reports)
BLOOD BILIRUBIN INCREASED ( 1 FDA reports)
BLOOD CALCIUM INCREASED ( 1 FDA reports)
BLOOD LACTATE DEHYDROGENASE INCREASED ( 1 FDA reports)
BREAKTHROUGH PAIN ( 1 FDA reports)
CARBOHYDRATE ANTIGEN 19-9 INCREASED ( 1 FDA reports)
CHEST PAIN ( 1 FDA reports)
COGNITIVE DISORDER ( 1 FDA reports)
COMPRESSION FRACTURE ( 1 FDA reports)
CONDUCTION DISORDER ( 1 FDA reports)
CYANOSIS ( 1 FDA reports)
DANDRUFF ( 1 FDA reports)
DILATATION VENTRICULAR ( 1 FDA reports)
DISORIENTATION ( 1 FDA reports)
DIZZINESS ( 1 FDA reports)
DRUG HYPERSENSITIVITY ( 1 FDA reports)
DRUG TOLERANCE ( 1 FDA reports)
DRY THROAT ( 1 FDA reports)
DUODENAL ULCER HAEMORRHAGE ( 1 FDA reports)
DYSPNOEA EXERTIONAL ( 1 FDA reports)
ELECTROCARDIOGRAM POOR R-WAVE PROGRESSION ( 1 FDA reports)
ELECTROCARDIOGRAM Q WAVE ABNORMAL ( 1 FDA reports)
ELECTROCARDIOGRAM T WAVE INVERSION ( 1 FDA reports)
ELECTROLYTE IMBALANCE ( 1 FDA reports)
EXCORIATION ( 1 FDA reports)
FACE OEDEMA ( 1 FDA reports)
FAECALOMA ( 1 FDA reports)
FEBRILE NEUTROPENIA ( 1 FDA reports)
FUNGAL INFECTION ( 1 FDA reports)
FUNGAL RASH ( 1 FDA reports)
GAMMA-GLUTAMYLTRANSFERASE INCREASED ( 1 FDA reports)
GASTROINTESTINAL HAEMORRHAGE ( 1 FDA reports)
GENERALISED ERYTHEMA ( 1 FDA reports)
GENERALISED OEDEMA ( 1 FDA reports)
HAEMOGLOBIN DECREASED ( 1 FDA reports)
HYDRONEPHROSIS ( 1 FDA reports)
HYPERAESTHESIA ( 1 FDA reports)
HYPERHIDROSIS ( 1 FDA reports)
HYPONATRAEMIA ( 1 FDA reports)
HYPOXIA ( 1 FDA reports)
INADEQUATE ANALGESIA ( 1 FDA reports)
INAPPROPRIATE SCHEDULE OF DRUG ADMINISTRATION ( 1 FDA reports)
INCORRECT ROUTE OF DRUG ADMINISTRATION ( 1 FDA reports)
INFLUENZA LIKE ILLNESS ( 1 FDA reports)
JAUNDICE ( 1 FDA reports)
LARYNGOMALACIA ( 1 FDA reports)
LARYNGOSPASM ( 1 FDA reports)
LIVER DISORDER ( 1 FDA reports)
MALAISE ( 1 FDA reports)
MEMORY IMPAIRMENT ( 1 FDA reports)
METASTASES TO ABDOMINAL CAVITY ( 1 FDA reports)
METASTASES TO BONE ( 1 FDA reports)
METASTASES TO CENTRAL NERVOUS SYSTEM ( 1 FDA reports)
METASTATIC NEOPLASM ( 1 FDA reports)
MITOCHONDRIAL MYOPATHY ( 1 FDA reports)
MULTIPLE CONGENITAL ABNORMALITIES ( 1 FDA reports)
MUSCULOSKELETAL CHEST PAIN ( 1 FDA reports)
MUSCULOSKELETAL STIFFNESS ( 1 FDA reports)
MYOCARDIAL INFARCTION ( 1 FDA reports)
MYOPATHY ( 1 FDA reports)
NASOPHARYNGEAL DISORDER ( 1 FDA reports)
NECK PAIN ( 1 FDA reports)
NEUROPATHY PERIPHERAL ( 1 FDA reports)
NEUROTOXICITY ( 1 FDA reports)
OVARIAN CANCER ( 1 FDA reports)
PANCREATITIS ACUTE ( 1 FDA reports)
PERIPHERAL VASCULAR DISORDER ( 1 FDA reports)
PHARYNGOLARYNGEAL PAIN ( 1 FDA reports)
PLEURAL EFFUSION ( 1 FDA reports)
PLEURAL RUB ( 1 FDA reports)
PLEURITIC PAIN ( 1 FDA reports)
PNEUMONIA ( 1 FDA reports)
PROCEDURAL PAIN ( 1 FDA reports)
PRURITUS ( 1 FDA reports)
PULMONARY EMBOLISM ( 1 FDA reports)
RASH ERYTHEMATOUS ( 1 FDA reports)
RECTAL HAEMORRHAGE ( 1 FDA reports)
SCREAMING ( 1 FDA reports)
SINUS TACHYCARDIA ( 1 FDA reports)
SKIN EXFOLIATION ( 1 FDA reports)
SWELLING ( 1 FDA reports)
SYSTOLIC HYPERTENSION ( 1 FDA reports)
THROMBOSIS ( 1 FDA reports)
TONSILLAR DISORDER ( 1 FDA reports)
TROPONIN INCREASED ( 1 FDA reports)
UROSEPSIS ( 1 FDA reports)
VENTRICULAR DYSFUNCTION ( 1 FDA reports)
VIRAL INFECTION ( 1 FDA reports)
VISION BLURRED ( 1 FDA reports)
WRONG TECHNIQUE IN DRUG USAGE PROCESS ( 1 FDA reports)

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