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

NAUSEA ( 18 FDA reports)
DIARRHOEA ( 16 FDA reports)
RASH ( 15 FDA reports)
ALOPECIA ( 14 FDA reports)
PLATELET COUNT DECREASED ( 14 FDA reports)
PYREXIA ( 14 FDA reports)
SEPSIS ( 14 FDA reports)
VOMITING ( 14 FDA reports)
ANAEMIA ( 12 FDA reports)
GASTROINTESTINAL HAEMORRHAGE ( 12 FDA reports)
ILEUS ( 12 FDA reports)
ILEUS PARALYTIC ( 12 FDA reports)
LIPASE INCREASED ( 12 FDA reports)
PLEURAL EFFUSION ( 12 FDA reports)
RENAL IMPAIRMENT ( 11 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 10 FDA reports)
HAEMOGLOBIN DECREASED ( 10 FDA reports)
FATIGUE ( 8 FDA reports)
PNEUMONIA ( 8 FDA reports)
PNEUMONIA ASPIRATION ( 8 FDA reports)
RETROPERITONEAL ABSCESS ( 8 FDA reports)
DECREASED APPETITE ( 7 FDA reports)
INTERSTITIAL LUNG DISEASE ( 7 FDA reports)
MALIGNANT NEOPLASM PROGRESSION ( 7 FDA reports)
PALMAR-PLANTAR ERYTHRODYSAESTHESIA SYNDROME ( 7 FDA reports)
WHITE BLOOD CELL COUNT DECREASED ( 7 FDA reports)
BLOOD ALKALINE PHOSPHATASE INCREASED ( 6 FDA reports)
DISSEMINATED INTRAVASCULAR COAGULATION ( 6 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 5 FDA reports)
DIZZINESS ( 5 FDA reports)
DYSPNOEA ( 5 FDA reports)
GAIT DISTURBANCE ( 5 FDA reports)
GAMMA-GLUTAMYLTRANSFERASE INCREASED ( 5 FDA reports)
HEPATIC NEOPLASM MALIGNANT ( 5 FDA reports)
BLOOD ALBUMIN DECREASED ( 4 FDA reports)
BLOOD LACTATE DEHYDROGENASE INCREASED ( 4 FDA reports)
C-REACTIVE PROTEIN INCREASED ( 4 FDA reports)
CONSTIPATION ( 4 FDA reports)
DEEP VEIN THROMBOSIS ( 4 FDA reports)
DEPRESSED LEVEL OF CONSCIOUSNESS ( 4 FDA reports)
ENTEROCOLITIS ( 4 FDA reports)
FALL ( 4 FDA reports)
FISTULA ( 4 FDA reports)
GASTRIC ULCER ( 4 FDA reports)
HAEMATOCRIT DECREASED ( 4 FDA reports)
HYPOPHAGIA ( 4 FDA reports)
INFLUENZA ( 4 FDA reports)
LUNG ADENOCARCINOMA ( 4 FDA reports)
RED BLOOD CELL COUNT DECREASED ( 4 FDA reports)
RENAL CELL CARCINOMA ( 4 FDA reports)
RENAL CELL CARCINOMA STAGE IV ( 4 FDA reports)
SOMNOLENCE ( 4 FDA reports)
WHITE BLOOD CELL COUNT INCREASED ( 4 FDA reports)
ARTHRALGIA ( 3 FDA reports)
ASCITES ( 3 FDA reports)
BLOOD BILIRUBIN INCREASED ( 3 FDA reports)
BLOOD CALCIUM INCREASED ( 3 FDA reports)
BLOOD CREATININE INCREASED ( 3 FDA reports)
BLOOD SODIUM DECREASED ( 3 FDA reports)
BREAST CANCER RECURRENT ( 3 FDA reports)
DYSPHAGIA ( 3 FDA reports)
DYSPHONIA ( 3 FDA reports)
ESCHERICHIA INFECTION ( 3 FDA reports)
FEMUR FRACTURE ( 3 FDA reports)
HYPERKALAEMIA ( 3 FDA reports)
LIVER DISORDER ( 3 FDA reports)
METASTASES TO MENINGES ( 3 FDA reports)
OVARIAN CANCER ( 3 FDA reports)
PULMONARY EMBOLISM ( 3 FDA reports)
RESPIRATORY DEPRESSION ( 3 FDA reports)
SENSATION OF FOREIGN BODY ( 3 FDA reports)
STOMATITIS ( 3 FDA reports)
ALLODYNIA ( 2 FDA reports)
ANALGESIC DRUG LEVEL INCREASED ( 2 FDA reports)
ARTHROPATHY ( 2 FDA reports)
BLOOD POTASSIUM INCREASED ( 2 FDA reports)
BLOOD URIC ACID INCREASED ( 2 FDA reports)
CANCER PAIN ( 2 FDA reports)
CARDIAC FAILURE ( 2 FDA reports)
CHILLS ( 2 FDA reports)
COLON CANCER RECURRENT ( 2 FDA reports)
COLORECTAL CANCER ( 2 FDA reports)
CONFUSIONAL STATE ( 2 FDA reports)
DIVERTICULITIS ( 2 FDA reports)
DYSURIA ( 2 FDA reports)
EMPHYSEMA ( 2 FDA reports)
ERYTHEMA ( 2 FDA reports)
FEBRILE NEUTROPENIA ( 2 FDA reports)
HYPERGLYCAEMIA ( 2 FDA reports)
INFECTION ( 2 FDA reports)
LETHARGY ( 2 FDA reports)
MELAENA ( 2 FDA reports)
NEOPLASM MALIGNANT ( 2 FDA reports)
NEUTROPHIL COUNT DECREASED ( 2 FDA reports)
OEDEMA PERIPHERAL ( 2 FDA reports)
PAIN ( 2 FDA reports)
PANCYTOPENIA ( 2 FDA reports)
RENAL FAILURE ACUTE ( 2 FDA reports)
RESTLESSNESS ( 2 FDA reports)
SOLILOQUY ( 2 FDA reports)
TUMOUR LYSIS SYNDROME ( 2 FDA reports)
URINARY RETENTION ( 2 FDA reports)
URINARY TRACT INFECTION ( 2 FDA reports)
URINE OUTPUT DECREASED ( 2 FDA reports)
WEIGHT DECREASED ( 2 FDA reports)
ABDOMINAL PAIN LOWER ( 1 FDA reports)
ABNORMAL BEHAVIOUR ( 1 FDA reports)
ABSCESS ( 1 FDA reports)
ANAL SPHINCTER ATONY ( 1 FDA reports)
ANOREXIA ( 1 FDA reports)
APPLICATION SITE ERYTHEMA ( 1 FDA reports)
APPLICATION SITE HAEMATOMA ( 1 FDA reports)
APPLICATION SITE PAIN ( 1 FDA reports)
ASTHENIA ( 1 FDA reports)
BACK PAIN ( 1 FDA reports)
BILE DUCT CANCER ( 1 FDA reports)
BLOOD CREATINE PHOSPHOKINASE INCREASED ( 1 FDA reports)
BLOOD GLUCOSE INCREASED ( 1 FDA reports)
BLOOD PH INCREASED ( 1 FDA reports)
BLOOD PRESSURE DECREASED ( 1 FDA reports)
BLOOD PRESSURE INCREASED ( 1 FDA reports)
CARDIAC ARREST ( 1 FDA reports)
CHOLECYSTITIS ( 1 FDA reports)
COLORECTAL CANCER RECURRENT ( 1 FDA reports)
CONDITION AGGRAVATED ( 1 FDA reports)
DEHYDRATION ( 1 FDA reports)
DERMATITIS ACNEIFORM ( 1 FDA reports)
DILATATION VENTRICULAR ( 1 FDA reports)
DISEASE PROGRESSION ( 1 FDA reports)
DISORIENTATION ( 1 FDA reports)
DRUG DOSE OMISSION ( 1 FDA reports)
DRUG ERUPTION ( 1 FDA reports)
DRUG INTERACTION ( 1 FDA reports)
EPISTAXIS ( 1 FDA reports)
ERUCTATION ( 1 FDA reports)
EXOPHTHALMOS ( 1 FDA reports)
FEELING ABNORMAL ( 1 FDA reports)
GASTRIC CANCER ( 1 FDA reports)
GASTRIC ULCER HAEMORRHAGE ( 1 FDA reports)
GENERAL PHYSICAL HEALTH DETERIORATION ( 1 FDA reports)
GLAUCOMA ( 1 FDA reports)
HAEMORRHAGE SUBCUTANEOUS ( 1 FDA reports)
HALLUCINATION ( 1 FDA reports)
HEADACHE ( 1 FDA reports)
HEPATIC FUNCTION ABNORMAL ( 1 FDA reports)
HERPES ZOSTER ( 1 FDA reports)
HYPERTENSION ( 1 FDA reports)
HYPOALBUMINAEMIA ( 1 FDA reports)
HYPOTENSION ( 1 FDA reports)
IMMUNOSUPPRESSION ( 1 FDA reports)
INFERIOR VENA CAVA DILATATION ( 1 FDA reports)
LEUKOPENIA ( 1 FDA reports)
LOSS OF CONSCIOUSNESS ( 1 FDA reports)
LUNG CONSOLIDATION ( 1 FDA reports)
LUNG DISORDER ( 1 FDA reports)
LUNG NEOPLASM MALIGNANT ( 1 FDA reports)
MALAISE ( 1 FDA reports)
MALIGNANT ASCITES ( 1 FDA reports)
MEDIASTINUM NEOPLASM ( 1 FDA reports)
MEDICATION ERROR ( 1 FDA reports)
METASTASES TO BONE ( 1 FDA reports)
METASTASES TO EYE ( 1 FDA reports)
METASTASES TO LIVER ( 1 FDA reports)
METASTASES TO PANCREAS ( 1 FDA reports)
METASTASES TO SPINE ( 1 FDA reports)
MONOPLEGIA ( 1 FDA reports)
NEOPLASM PROGRESSION ( 1 FDA reports)
NERVE DEGENERATION ( 1 FDA reports)
NEUROGENIC BLADDER ( 1 FDA reports)
NEUTROPENIA ( 1 FDA reports)
NEUTROPHIL COUNT INCREASED ( 1 FDA reports)
NEUTROPHIL TOXIC GRANULATION PRESENT ( 1 FDA reports)
NON-SMALL CELL LUNG CANCER ( 1 FDA reports)
NON-SMALL CELL LUNG CANCER METASTATIC ( 1 FDA reports)
OCCULT BLOOD POSITIVE ( 1 FDA reports)
OESOPHAGEAL OBSTRUCTION ( 1 FDA reports)
OESOPHAGEAL STENOSIS ( 1 FDA reports)
OESOPHAGITIS ( 1 FDA reports)
OESOPHAGOBRONCHIAL FISTULA ( 1 FDA reports)
PANCREATIC CARCINOMA ( 1 FDA reports)
PLATELET COUNT INCREASED ( 1 FDA reports)
PNEUMOCYSTIS JIROVECI PNEUMONIA ( 1 FDA reports)
PNEUMONIA BACTERIAL ( 1 FDA reports)
PNEUMONITIS ( 1 FDA reports)
PRODUCT QUALITY ISSUE ( 1 FDA reports)
PROSTATE CANCER ( 1 FDA reports)
PROTEIN TOTAL DECREASED ( 1 FDA reports)
PRURITUS ( 1 FDA reports)
PULMONARY HYPERTENSION ( 1 FDA reports)
PULMONARY MASS ( 1 FDA reports)
RESPIRATORY ARREST ( 1 FDA reports)
RIGHT ATRIAL DILATATION ( 1 FDA reports)
ROAD TRAFFIC ACCIDENT ( 1 FDA reports)
SERUM FERRITIN DECREASED ( 1 FDA reports)
STENT PLACEMENT ( 1 FDA reports)
STERNAL FRACTURE ( 1 FDA reports)
SWELLING ( 1 FDA reports)
TOXIC SKIN ERUPTION ( 1 FDA reports)
TRACHEO-OESOPHAGEAL FISTULA ( 1 FDA reports)
TREMOR ( 1 FDA reports)
TUMOUR NECROSIS ( 1 FDA reports)
WEIGHT INCREASED ( 1 FDA reports)
WRONG TECHNIQUE IN DRUG USAGE PROCESS ( 1 FDA reports)

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