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

NAUSEA ( 20 FDA reports)
VOMITING ( 17 FDA reports)
PYREXIA ( 13 FDA reports)
NEUTROPENIA ( 12 FDA reports)
DIARRHOEA ( 11 FDA reports)
PAIN ( 11 FDA reports)
THROMBOCYTOPENIA ( 9 FDA reports)
CARDIAC FAILURE CONGESTIVE ( 8 FDA reports)
DEHYDRATION ( 8 FDA reports)
FATIGUE ( 8 FDA reports)
ANAEMIA ( 7 FDA reports)
ANOREXIA ( 7 FDA reports)
DEATH ( 7 FDA reports)
DYSPNOEA ( 7 FDA reports)
FEBRILE NEUTROPENIA ( 7 FDA reports)
GASTROINTESTINAL HAEMORRHAGE ( 7 FDA reports)
MYALGIA ( 6 FDA reports)
OEDEMA PERIPHERAL ( 6 FDA reports)
THROMBOSIS ( 6 FDA reports)
ARTHRALGIA ( 5 FDA reports)
ASTHENIA ( 5 FDA reports)
DISSEMINATED INTRAVASCULAR COAGULATION ( 5 FDA reports)
FLUID RETENTION ( 5 FDA reports)
GENERAL PHYSICAL HEALTH DETERIORATION ( 5 FDA reports)
HYPOTENSION ( 5 FDA reports)
INCORRECT ROUTE OF DRUG ADMINISTRATION ( 5 FDA reports)
PLATELET COUNT DECREASED ( 5 FDA reports)
RENAL FAILURE ( 5 FDA reports)
STOMATITIS ( 5 FDA reports)
ABDOMINAL PAIN ( 4 FDA reports)
CARDIAC AMYLOIDOSIS ( 4 FDA reports)
DECREASED APPETITE ( 4 FDA reports)
DISEASE PROGRESSION ( 4 FDA reports)
FUNGAL INFECTION ( 4 FDA reports)
HYPERSENSITIVITY ( 4 FDA reports)
HYPERTENSION ( 4 FDA reports)
JOINT SWELLING ( 4 FDA reports)
MALAISE ( 4 FDA reports)
SEPSIS ( 4 FDA reports)
ACUTE HEPATIC FAILURE ( 3 FDA reports)
BACK PAIN ( 3 FDA reports)
BLOOD TEST ABNORMAL ( 3 FDA reports)
BONE MARROW DEPRESSION ( 3 FDA reports)
CLOSTRIDIUM DIFFICILE COLITIS ( 3 FDA reports)
COAGULOPATHY ( 3 FDA reports)
CONTUSION ( 3 FDA reports)
CONVULSION ( 3 FDA reports)
COUGH ( 3 FDA reports)
DEPRESSED LEVEL OF CONSCIOUSNESS ( 3 FDA reports)
DIZZINESS ( 3 FDA reports)
DRUG TOXICITY ( 3 FDA reports)
ERYTHEMA ( 3 FDA reports)
FALL ( 3 FDA reports)
GAIT DISTURBANCE ( 3 FDA reports)
GAZE PALSY ( 3 FDA reports)
HAEMATURIA ( 3 FDA reports)
HEADACHE ( 3 FDA reports)
HEPATIC FAILURE ( 3 FDA reports)
HEPATOMEGALY ( 3 FDA reports)
HYPOPERFUSION ( 3 FDA reports)
INFECTION ( 3 FDA reports)
INTERNATIONAL NORMALISED RATIO INCREASED ( 3 FDA reports)
MALIGNANT NEOPLASM PROGRESSION ( 3 FDA reports)
MUSCULOSKELETAL DISCOMFORT ( 3 FDA reports)
NEUROPATHY PERIPHERAL ( 3 FDA reports)
OSTEONECROSIS ( 3 FDA reports)
PANCYTOPENIA ( 3 FDA reports)
PNEUMONIA ( 3 FDA reports)
POSTURING ( 3 FDA reports)
PROCEDURAL COMPLICATION ( 3 FDA reports)
RECTAL HAEMORRHAGE ( 3 FDA reports)
RENAL FAILURE ACUTE ( 3 FDA reports)
SICKLE CELL ANAEMIA WITH CRISIS ( 3 FDA reports)
SYNCOPE ( 3 FDA reports)
TOOTH LOSS ( 3 FDA reports)
TRANSAMINASES INCREASED ( 3 FDA reports)
UNRESPONSIVE TO STIMULI ( 3 FDA reports)
ABDOMINAL DISCOMFORT ( 2 FDA reports)
ABDOMINAL PAIN LOWER ( 2 FDA reports)
ABDOMINAL TENDERNESS ( 2 FDA reports)
ABSCESS ( 2 FDA reports)
ACUTE MYOCARDIAL INFARCTION ( 2 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 2 FDA reports)
ALOPECIA ( 2 FDA reports)
ANAEMIA HAEMOLYTIC AUTOIMMUNE ( 2 FDA reports)
AORTIC VALVE DISEASE ( 2 FDA reports)
ASCITES ( 2 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 2 FDA reports)
ATTENTION DEFICIT/HYPERACTIVITY DISORDER ( 2 FDA reports)
BACTERIAL INFECTION ( 2 FDA reports)
BLOOD ALKALINE PHOSPHATASE INCREASED ( 2 FDA reports)
BLOOD CREATININE INCREASED ( 2 FDA reports)
CEREBRAL ARTERY EMBOLISM ( 2 FDA reports)
CEREBRAL HAEMORRHAGE ( 2 FDA reports)
CEREBROVASCULAR ACCIDENT ( 2 FDA reports)
CHEST PAIN ( 2 FDA reports)
CHILLS ( 2 FDA reports)
COGNITIVE DISORDER ( 2 FDA reports)
COLITIS ( 2 FDA reports)
COOMBS TEST POSITIVE ( 2 FDA reports)
DEVICE RELATED INFECTION ( 2 FDA reports)
DRUG EFFECT DECREASED ( 2 FDA reports)
DRUG HYPERSENSITIVITY ( 2 FDA reports)
EMBOLIC CEREBRAL INFARCTION ( 2 FDA reports)
EMBOLISM ( 2 FDA reports)
EMOTIONAL DISTRESS ( 2 FDA reports)
ENDOCARDITIS ( 2 FDA reports)
HAEMORRHAGE ( 2 FDA reports)
HAEMORRHAGE INTRACRANIAL ( 2 FDA reports)
HAEMORRHAGIC TRANSFORMATION STROKE ( 2 FDA reports)
HYPERBILIRUBINAEMIA ( 2 FDA reports)
HYPERGLYCAEMIA ( 2 FDA reports)
HYPOCALCAEMIA ( 2 FDA reports)
INFLAMMATION ( 2 FDA reports)
INTENTIONAL OVERDOSE ( 2 FDA reports)
INTRACRANIAL VENOUS SINUS THROMBOSIS ( 2 FDA reports)
JAUNDICE ( 2 FDA reports)
LEUKAEMIA ( 2 FDA reports)
LEUKOCYTOSIS ( 2 FDA reports)
LOSS OF CONSCIOUSNESS ( 2 FDA reports)
MELAENA ( 2 FDA reports)
MELAS SYNDROME ( 2 FDA reports)
MENSTRUATION IRREGULAR ( 2 FDA reports)
MENTAL DISORDER ( 2 FDA reports)
MIGRAINE ( 2 FDA reports)
MUCOSAL INFLAMMATION ( 2 FDA reports)
MULTI-ORGAN FAILURE ( 2 FDA reports)
MYELODYSPLASTIC SYNDROME ( 2 FDA reports)
NAIL DISORDER ( 2 FDA reports)
NASOPHARYNGITIS ( 2 FDA reports)
NEUTROPENIC INFECTION ( 2 FDA reports)
OCULAR ICTERUS ( 2 FDA reports)
OEDEMA ( 2 FDA reports)
OSTEOMYELITIS ( 2 FDA reports)
PAIN IN EXTREMITY ( 2 FDA reports)
PALMAR-PLANTAR ERYTHRODYSAESTHESIA SYNDROME ( 2 FDA reports)
PERIPHERAL SENSORY NEUROPATHY ( 2 FDA reports)
PHOTOPHOBIA ( 2 FDA reports)
PROTEINURIA ( 2 FDA reports)
PSEUDOMONAL BACTERAEMIA ( 2 FDA reports)
SEPTIC SHOCK ( 2 FDA reports)
STEM CELL TRANSPLANT ( 2 FDA reports)
SUDDEN DEATH ( 2 FDA reports)
SWELLING ( 2 FDA reports)
TINNITUS ( 2 FDA reports)
TOOTH DISCOLOURATION ( 2 FDA reports)
VASCULITIS ( 2 FDA reports)
WEIGHT DECREASED ( 2 FDA reports)
ABASIA ( 1 FDA reports)
ABDOMINAL MASS ( 1 FDA reports)
ACCIDENTAL POISONING ( 1 FDA reports)
AGGRESSION ( 1 FDA reports)
AGITATION ( 1 FDA reports)
ALCOHOL ABUSE ( 1 FDA reports)
AMNIOTIC BAND SYNDROME ( 1 FDA reports)
ANGINA PECTORIS ( 1 FDA reports)
ANGINA UNSTABLE ( 1 FDA reports)
ARTERIOSCLEROSIS CORONARY ARTERY ( 1 FDA reports)
ARTHRITIS BACTERIAL ( 1 FDA reports)
ATELECTASIS ( 1 FDA reports)
BACTERAEMIA ( 1 FDA reports)
BILIARY TRACT DISORDER ( 1 FDA reports)
BILIRUBIN CONJUGATED INCREASED ( 1 FDA reports)
BLOOD AMINO ACID LEVEL INCREASED ( 1 FDA reports)
BLOOD BILIRUBIN INCREASED ( 1 FDA reports)
BLOOD BILIRUBIN UNCONJUGATED INCREASED ( 1 FDA reports)
BLOOD CALCIUM DECREASED ( 1 FDA reports)
BLOOD ELECTROLYTES ABNORMAL ( 1 FDA reports)
BLOOD GLUCOSE INCREASED ( 1 FDA reports)
BLOOD LACTATE DEHYDROGENASE INCREASED ( 1 FDA reports)
BLOOD PRESSURE DECREASED ( 1 FDA reports)
BODY TEMPERATURE INCREASED ( 1 FDA reports)
BOWEL SOUNDS ABNORMAL ( 1 FDA reports)
BRAIN OEDEMA ( 1 FDA reports)
BREAST CANCER ( 1 FDA reports)
BRONCHOPULMONARY ASPERGILLOSIS ( 1 FDA reports)
CARDIAC ARREST ( 1 FDA reports)
CARDIAC FAILURE ( 1 FDA reports)
CARDIAC MURMUR ( 1 FDA reports)
CARDIAC SEPTAL DEFECT ( 1 FDA reports)
CARDIOMYOPATHY ( 1 FDA reports)
CARDIOTOXICITY ( 1 FDA reports)
CATABOLIC STATE ( 1 FDA reports)
CEREBRAL ARTERY OCCLUSION ( 1 FDA reports)
CHEST DISCOMFORT ( 1 FDA reports)
CHROMOSOME ABNORMALITY ( 1 FDA reports)
CIRCULATORY COLLAPSE ( 1 FDA reports)
CLEFT LIP AND PALATE ( 1 FDA reports)
COLITIS MICROSCOPIC ( 1 FDA reports)
CONDITION AGGRAVATED ( 1 FDA reports)
CONGENITAL ANOMALY ( 1 FDA reports)
CONGENITAL CENTRAL NERVOUS SYSTEM ANOMALY ( 1 FDA reports)
CONGENITAL EYE DISORDER ( 1 FDA reports)
CONGENITAL GENITAL MALFORMATION ( 1 FDA reports)
CONGENITAL MUSCULOSKELETAL ANOMALY ( 1 FDA reports)
CONSTIPATION ( 1 FDA reports)
CREPITATIONS ( 1 FDA reports)
CYST ( 1 FDA reports)
DECREASED ACTIVITY ( 1 FDA reports)
DECUBITUS ULCER ( 1 FDA reports)
DENTAL CARIES ( 1 FDA reports)
DEPRESSION ( 1 FDA reports)
DERMAL CYST ( 1 FDA reports)
DIFFICULTY IN WALKING ( 1 FDA reports)
DISEASE RECURRENCE ( 1 FDA reports)
DRUG DEPENDENCE ( 1 FDA reports)
DRUG EXPOSURE DURING PREGNANCY ( 1 FDA reports)
DRUG INEFFECTIVE ( 1 FDA reports)
DRUG PRESCRIBING ERROR ( 1 FDA reports)
DRUG WITHDRAWAL SYNDROME ( 1 FDA reports)
DYSMORPHISM ( 1 FDA reports)
DYSTONIA ( 1 FDA reports)
EAR MALFORMATION ( 1 FDA reports)
EARLY SATIETY ( 1 FDA reports)
EPISTAXIS ( 1 FDA reports)
EPSTEIN-BARR VIRUS INFECTION ( 1 FDA reports)
ERYSIPELAS ( 1 FDA reports)
EXTREMITY NECROSIS ( 1 FDA reports)
FEBRILE BONE MARROW APLASIA ( 1 FDA reports)
FEELING ABNORMAL ( 1 FDA reports)
FINGER AMPUTATION ( 1 FDA reports)
FLATULENCE ( 1 FDA reports)
FLUID OVERLOAD ( 1 FDA reports)
GAMMA-GLUTAMYLTRANSFERASE INCREASED ( 1 FDA reports)
GASTRITIS ( 1 FDA reports)
GASTROINTESTINAL INFECTION ( 1 FDA reports)
GASTROINTESTINAL MALFORMATION ( 1 FDA reports)
GASTROINTESTINAL TOXICITY ( 1 FDA reports)
GLOSSODYNIA ( 1 FDA reports)
GROIN PAIN ( 1 FDA reports)
HAEMATEMESIS ( 1 FDA reports)
HAEMATOCRIT DECREASED ( 1 FDA reports)
HAEMOGLOBIN DECREASED ( 1 FDA reports)
HAEMOLYTIC URAEMIC SYNDROME ( 1 FDA reports)
HEART DISEASE CONGENITAL ( 1 FDA reports)
HEART RATE INCREASED ( 1 FDA reports)
HEMIPARESIS ( 1 FDA reports)
HEPATIC FUNCTION ABNORMAL ( 1 FDA reports)
HEPATITIS ( 1 FDA reports)
HEPATOCELLULAR DAMAGE ( 1 FDA reports)
HEPATOTOXICITY ( 1 FDA reports)
HEREDITARY ANGIOEDEMA ( 1 FDA reports)
HYPERTHERMIA ( 1 FDA reports)
HYPOALBUMINAEMIA ( 1 FDA reports)
HYPONATRAEMIA ( 1 FDA reports)
IDIOPATHIC THROMBOCYTOPENIC PURPURA ( 1 FDA reports)
ILLUSION ( 1 FDA reports)
IMPAIRED HEALING ( 1 FDA reports)
INFUSION RELATED REACTION ( 1 FDA reports)
INSOMNIA ( 1 FDA reports)
INTESTINAL OBSTRUCTION ( 1 FDA reports)
LANGERHANS' CELL HISTIOCYTOSIS ( 1 FDA reports)
LETHARGY ( 1 FDA reports)
LEUKOENCEPHALOPATHY ( 1 FDA reports)
LEUKOPENIA ( 1 FDA reports)
LIMB DEFORMITY ( 1 FDA reports)
LIMB MALFORMATION ( 1 FDA reports)
LIMB TRAUMATIC AMPUTATION ( 1 FDA reports)
LIVER FUNCTION TEST ABNORMAL ( 1 FDA reports)
LOOSE TOOTH ( 1 FDA reports)
LYMPHADENOPATHY ( 1 FDA reports)
LYMPHOMA ( 1 FDA reports)
MALNUTRITION ( 1 FDA reports)
MANIA ( 1 FDA reports)
MATERNAL EXPOSURE DURING PREGNANCY ( 1 FDA reports)
MEMORY IMPAIRMENT ( 1 FDA reports)
MENTAL STATUS CHANGES ( 1 FDA reports)
METABOLIC ACIDOSIS ( 1 FDA reports)
METASTASES TO BONE ( 1 FDA reports)
MUSCLE CRAMP ( 1 FDA reports)
MUSCLE SPASMS ( 1 FDA reports)
MUSCULAR WEAKNESS ( 1 FDA reports)
MUSCULOSKELETAL DEFORMITY ( 1 FDA reports)
MUSCULOSKELETAL PAIN ( 1 FDA reports)
MUSCULOSKELETAL STIFFNESS ( 1 FDA reports)
MYOCARDIAL INFARCTION ( 1 FDA reports)
NECK PAIN ( 1 FDA reports)
NECROSIS ( 1 FDA reports)
NEURALGIA ( 1 FDA reports)
NEUROLOGICAL SYMPTOM ( 1 FDA reports)
NEUROMA ( 1 FDA reports)
NEUROTOXICITY ( 1 FDA reports)
NEUTROPENIC SEPSIS ( 1 FDA reports)
NEUTROPHIL COUNT DECREASED ( 1 FDA reports)
OBSTRUCTIVE AIRWAYS DISORDER ( 1 FDA reports)
OLIGOHYDRAMNIOS ( 1 FDA reports)
OVARIAN CANCER ( 1 FDA reports)
OVARIAN CANCER METASTATIC ( 1 FDA reports)
PAIN EXACERBATED ( 1 FDA reports)
PAIN IN JAW ( 1 FDA reports)
PANCREATITIS ( 1 FDA reports)
PANCREATITIS ACUTE ( 1 FDA reports)
PCO2 DECREASED ( 1 FDA reports)
PEPTIC ULCER ( 1 FDA reports)
PERICARDIAL EFFUSION ( 1 FDA reports)
PERIORBITAL OEDEMA ( 1 FDA reports)
PERITONEAL DISORDER ( 1 FDA reports)
PERITONEAL TUBERCULOSIS ( 1 FDA reports)
PERITONITIS BACTERIAL ( 1 FDA reports)
PETECHIAE ( 1 FDA reports)
PHLEBITIS INFECTIVE ( 1 FDA reports)
PLATELET COUNT ABNORMAL ( 1 FDA reports)
PLEURAL EFFUSION ( 1 FDA reports)
PLEURITIC PAIN ( 1 FDA reports)
PNEUMATIC COMPRESSION THERAPY ( 1 FDA reports)
PROSTATE CANCER METASTATIC ( 1 FDA reports)
PRURITUS ( 1 FDA reports)
PULMONARY EMBOLISM ( 1 FDA reports)
RADIOTHERAPY TO BONE ( 1 FDA reports)
RASH PRURITIC ( 1 FDA reports)
RESPIRATORY TRACT MALFORMATION ( 1 FDA reports)
RESTLESSNESS ( 1 FDA reports)
RETICULOCYTE COUNT INCREASED ( 1 FDA reports)
SHOCK HAEMORRHAGIC ( 1 FDA reports)
SINUSITIS ( 1 FDA reports)
SKIN EXFOLIATION ( 1 FDA reports)
SOFT TISSUE INFECTION ( 1 FDA reports)
SPINA BIFIDA ( 1 FDA reports)
SPLENOMEGALY ( 1 FDA reports)
STAPHYLOCOCCAL SEPSIS ( 1 FDA reports)
STREPTOCOCCAL INFECTION ( 1 FDA reports)
SUBDURAL HAEMATOMA ( 1 FDA reports)
SUICIDE ATTEMPT ( 1 FDA reports)
SWELLING FACE ( 1 FDA reports)
SWOLLEN TONGUE ( 1 FDA reports)
THERAPY NON-RESPONDER ( 1 FDA reports)
THROMBOPHLEBITIS ( 1 FDA reports)
TONSILLAR HYPERTROPHY ( 1 FDA reports)
TOOTH EXTRACTION ( 1 FDA reports)
TOOTHACHE ( 1 FDA reports)
TOXIC SKIN ERUPTION ( 1 FDA reports)
UPPER RESPIRATORY TRACT INFECTION ( 1 FDA reports)
URINARY RETENTION ( 1 FDA reports)
URINARY TRACT INFECTION ( 1 FDA reports)
URINARY TRACT MALFORMATION ( 1 FDA reports)
VASCULAR ANOMALY ( 1 FDA reports)
WHITE BLOOD CELL COUNT DECREASED ( 1 FDA reports)
WRONG TECHNIQUE IN DRUG USAGE PROCESS ( 1 FDA reports)
X-RAY GASTROINTESTINAL TRACT ABNORMAL ( 1 FDA reports)

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