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

PYREXIA ( 21 FDA reports)
MALAISE ( 16 FDA reports)
VOMITING ( 15 FDA reports)
INTERSTITIAL LUNG DISEASE ( 14 FDA reports)
PLATELET COUNT DECREASED ( 14 FDA reports)
RASH ( 14 FDA reports)
DIARRHOEA ( 12 FDA reports)
NAUSEA ( 12 FDA reports)
PNEUMONIA PNEUMOCOCCAL ( 12 FDA reports)
ANAEMIA ( 11 FDA reports)
ACUTE RESPIRATORY DISTRESS SYNDROME ( 9 FDA reports)
FALL ( 9 FDA reports)
HYPERTENSION ( 9 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 8 FDA reports)
CONSTIPATION ( 8 FDA reports)
DECREASED APPETITE ( 8 FDA reports)
DYSPEPSIA ( 8 FDA reports)
OEDEMA PERIPHERAL ( 8 FDA reports)
ASCITES ( 7 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 7 FDA reports)
BLOOD PRESSURE INCREASED ( 7 FDA reports)
CARDIAC ARREST ( 7 FDA reports)
DIZZINESS ( 7 FDA reports)
DRUG INTERACTION ( 7 FDA reports)
DYSPNOEA ( 7 FDA reports)
HEADACHE ( 7 FDA reports)
HEPATIC FUNCTION ABNORMAL ( 7 FDA reports)
LIVER DISORDER ( 7 FDA reports)
OTITIS MEDIA ( 7 FDA reports)
PALMAR-PLANTAR ERYTHRODYSAESTHESIA SYNDROME ( 7 FDA reports)
RENAL DISORDER ( 7 FDA reports)
RENAL FAILURE ACUTE ( 7 FDA reports)
STOMATITIS ( 7 FDA reports)
UPPER RESPIRATORY TRACT INFECTION ( 7 FDA reports)
ANOREXIA ( 6 FDA reports)
ANXIETY ( 6 FDA reports)
DEHYDRATION ( 6 FDA reports)
DEPRESSED LEVEL OF CONSCIOUSNESS ( 6 FDA reports)
DRUG INEFFECTIVE ( 6 FDA reports)
DRY SKIN ( 6 FDA reports)
ERYTHEMA ( 6 FDA reports)
PNEUMOCYSTIS JIROVECI PNEUMONIA ( 6 FDA reports)
ABDOMINAL DISTENSION ( 5 FDA reports)
ACNE ( 5 FDA reports)
ANGINA PECTORIS ( 5 FDA reports)
ATRIAL FIBRILLATION ( 5 FDA reports)
BACK PAIN ( 5 FDA reports)
BLOOD ALKALINE PHOSPHATASE INCREASED ( 5 FDA reports)
C-REACTIVE PROTEIN INCREASED ( 5 FDA reports)
COLITIS ISCHAEMIC ( 5 FDA reports)
DEPRESSION ( 5 FDA reports)
GENERALISED OEDEMA ( 5 FDA reports)
HEPATIC NEOPLASM MALIGNANT ( 5 FDA reports)
HYPERURICAEMIA ( 5 FDA reports)
MYRINGITIS ( 5 FDA reports)
ORAL INTAKE REDUCED ( 5 FDA reports)
PLEURAL EFFUSION ( 5 FDA reports)
PULMONARY EMBOLISM ( 5 FDA reports)
RESPIRATORY FAILURE ( 5 FDA reports)
SUBARACHNOID HAEMORRHAGE ( 5 FDA reports)
WHITE BLOOD CELL COUNT DECREASED ( 5 FDA reports)
ASTHENIA ( 4 FDA reports)
CARDIAC FAILURE ( 4 FDA reports)
CARDIAC FAILURE ACUTE ( 4 FDA reports)
CARDIAC FAILURE CONGESTIVE ( 4 FDA reports)
CARDIOMEGALY ( 4 FDA reports)
CATARACT ( 4 FDA reports)
CONVULSION ( 4 FDA reports)
CYTOMEGALOVIRUS INFECTION ( 4 FDA reports)
DEATH ( 4 FDA reports)
DEEP VEIN THROMBOSIS ( 4 FDA reports)
DYSPHAGIA ( 4 FDA reports)
ENTEROCOLITIS INFECTIOUS ( 4 FDA reports)
FOOD POISONING ( 4 FDA reports)
GASTROINTESTINAL MOTILITY DISORDER ( 4 FDA reports)
INAPPROPRIATE ANTIDIURETIC HORMONE SECRETION ( 4 FDA reports)
MALIGNANT ASCITES ( 4 FDA reports)
METASTASES TO LYMPH NODES ( 4 FDA reports)
MUSCLE SPASMS ( 4 FDA reports)
NEPHROTIC SYNDROME ( 4 FDA reports)
PAIN OF SKIN ( 4 FDA reports)
PULMONARY OEDEMA ( 4 FDA reports)
RESPIRATORY ARREST ( 4 FDA reports)
SHOCK ( 4 FDA reports)
SUBDURAL HAEMATOMA ( 4 FDA reports)
TENDON RUPTURE ( 4 FDA reports)
THROMBOCYTOPENIA ( 4 FDA reports)
URTICARIA ( 4 FDA reports)
ABDOMINAL PAIN LOWER ( 3 FDA reports)
ABDOMINAL PAIN UPPER ( 3 FDA reports)
ACTIVITIES OF DAILY LIVING IMPAIRED ( 3 FDA reports)
ATYPICAL MYCOBACTERIAL INFECTION ( 3 FDA reports)
BLOOD ALBUMIN DECREASED ( 3 FDA reports)
BLOOD CREATINE PHOSPHOKINASE INCREASED ( 3 FDA reports)
CEREBRAL INFARCTION ( 3 FDA reports)
COMA ( 3 FDA reports)
CONDITION AGGRAVATED ( 3 FDA reports)
CONFUSIONAL STATE ( 3 FDA reports)
DISEASE PROGRESSION ( 3 FDA reports)
DRUG HYPERSENSITIVITY ( 3 FDA reports)
DYSPNOEA EXERTIONAL ( 3 FDA reports)
DYSURIA ( 3 FDA reports)
FACE OEDEMA ( 3 FDA reports)
FATIGUE ( 3 FDA reports)
GASTRIC CANCER ( 3 FDA reports)
GENERALISED ERYTHEMA ( 3 FDA reports)
HAEMOGLOBIN DECREASED ( 3 FDA reports)
HEPATIC ENCEPHALOPATHY ( 3 FDA reports)
HYPONATRAEMIA ( 3 FDA reports)
INFECTION ( 3 FDA reports)
INSOMNIA ( 3 FDA reports)
INTESTINAL ISCHAEMIA ( 3 FDA reports)
JAUNDICE ( 3 FDA reports)
MUCOUS MEMBRANE DISORDER ( 3 FDA reports)
MUSCLE RIGIDITY ( 3 FDA reports)
OEDEMA ( 3 FDA reports)
PAIN ( 3 FDA reports)
PARALYSIS ( 3 FDA reports)
PNEUMOCYSTIS CARINII PNEUMONIA ( 3 FDA reports)
PUPILLARY LIGHT REFLEX TESTS ABNORMAL ( 3 FDA reports)
RASH ERYTHEMATOUS ( 3 FDA reports)
SUBDURAL HAEMATOMA EVACUATION ( 3 FDA reports)
THERAPEUTIC RESPONSE DECREASED ( 3 FDA reports)
TOOTHACHE ( 3 FDA reports)
ABDOMINAL PAIN ( 2 FDA reports)
ABNORMAL FAECES ( 2 FDA reports)
AGRANULOCYTOSIS ( 2 FDA reports)
ALTERED STATE OF CONSCIOUSNESS ( 2 FDA reports)
ANAPHYLACTOID REACTION ( 2 FDA reports)
ANOSMIA ( 2 FDA reports)
APPENDICITIS PERFORATED ( 2 FDA reports)
APTYALISM ( 2 FDA reports)
ARTHRALGIA ( 2 FDA reports)
BENIGN PROSTATIC HYPERPLASIA ( 2 FDA reports)
BLADDER CANCER ( 2 FDA reports)
BLOOD GLUCOSE DECREASED ( 2 FDA reports)
BLOOD LACTATE DEHYDROGENASE INCREASED ( 2 FDA reports)
BLOOD PRESSURE DECREASED ( 2 FDA reports)
BLOOD PRESSURE SYSTOLIC DECREASED ( 2 FDA reports)
BRADYCARDIA ( 2 FDA reports)
BRAIN OEDEMA ( 2 FDA reports)
BREAST SWELLING ( 2 FDA reports)
BUNDLE BRANCH BLOCK RIGHT ( 2 FDA reports)
CATARACT OPERATION ( 2 FDA reports)
CEREBELLAR ATAXIA ( 2 FDA reports)
CEREBRAL HAEMORRHAGE ( 2 FDA reports)
CHEILITIS ( 2 FDA reports)
CHEST PAIN ( 2 FDA reports)
CHILLS ( 2 FDA reports)
CONJUNCTIVITIS ( 2 FDA reports)
CONTUSION ( 2 FDA reports)
CYSTITIS ( 2 FDA reports)
DIPLOPIA ( 2 FDA reports)
DISSEMINATED INTRAVASCULAR COAGULATION ( 2 FDA reports)
DIZZINESS POSTURAL ( 2 FDA reports)
DRUG EFFECT DECREASED ( 2 FDA reports)
DRY EYE ( 2 FDA reports)
DRY MOUTH ( 2 FDA reports)
DYSPHONIA ( 2 FDA reports)
EPIPHYSIOLYSIS ( 2 FDA reports)
EYELID OEDEMA ( 2 FDA reports)
FEMUR FRACTURE ( 2 FDA reports)
GAIT DISTURBANCE ( 2 FDA reports)
GAMMA-GLUTAMYLTRANSFERASE INCREASED ( 2 FDA reports)
GASTRIC DISORDER ( 2 FDA reports)
GASTRIC ULCER ( 2 FDA reports)
GASTRIC ULCER HAEMORRHAGE ( 2 FDA reports)
GENERAL PHYSICAL HEALTH DETERIORATION ( 2 FDA reports)
HAEMORRHAGE SUBCUTANEOUS ( 2 FDA reports)
HALLUCINATION ( 2 FDA reports)
HERPES SIMPLEX ( 2 FDA reports)
HYPOKALAEMIA ( 2 FDA reports)
HYPOTHYROIDISM ( 2 FDA reports)
HYPOXIA ( 2 FDA reports)
IDIOPATHIC THROMBOCYTOPENIC PURPURA ( 2 FDA reports)
ILEUS PARALYTIC ( 2 FDA reports)
ILL-DEFINED DISORDER ( 2 FDA reports)
INFUSION RELATED REACTION ( 2 FDA reports)
INTUBATION ( 2 FDA reports)
IRON DEFICIENCY ANAEMIA ( 2 FDA reports)
LABORATORY TEST ABNORMAL ( 2 FDA reports)
LARGE GRANULAR LYMPHOCYTOSIS ( 2 FDA reports)
LOSS OF CONSCIOUSNESS ( 2 FDA reports)
MALIGNANT NEOPLASM PROGRESSION ( 2 FDA reports)
METASTASES TO CENTRAL NERVOUS SYSTEM ( 2 FDA reports)
MULTI-ORGAN FAILURE ( 2 FDA reports)
MUSCULOSKELETAL STIFFNESS ( 2 FDA reports)
MYALGIA ( 2 FDA reports)
NEUTROPENIA ( 2 FDA reports)
NEUTROPHIL COUNT DECREASED ( 2 FDA reports)
NIPPLE PAIN ( 2 FDA reports)
OSTEOMYELITIS ( 2 FDA reports)
PANCREATIC CARCINOMA METASTATIC ( 2 FDA reports)
PERITONITIS ( 2 FDA reports)
PLATELET COUNT INCREASED ( 2 FDA reports)
PNEUMOCYSTIS JIROVECI INFECTION ( 2 FDA reports)
PNEUMONIA ( 2 FDA reports)
POLYMYALGIA RHEUMATICA ( 2 FDA reports)
POLYNEUROPATHY ( 2 FDA reports)
PROCEDURAL HYPOTENSION ( 2 FDA reports)
PROSTATE CANCER ( 2 FDA reports)
PROTEIN URINE PRESENT ( 2 FDA reports)
PROTEINURIA ( 2 FDA reports)
PROTHROMBIN TIME PROLONGED ( 2 FDA reports)
PULMONARY ARTERY ANEURYSM ( 2 FDA reports)
PURPURA ( 2 FDA reports)
PYELONEPHRITIS ( 2 FDA reports)
RADIAL NERVE PALSY ( 2 FDA reports)
RESTLESS LEGS SYNDROME ( 2 FDA reports)
RHABDOMYOLYSIS ( 2 FDA reports)
SEPSIS ( 2 FDA reports)
SOMNOLENCE ( 2 FDA reports)
STAPHYLOCOCCAL INFECTION ( 2 FDA reports)
STAPHYLOCOCCAL SEPSIS ( 2 FDA reports)
TESTICULAR SWELLING ( 2 FDA reports)
URINE OUTPUT DECREASED ( 2 FDA reports)
WHITE BLOOD CELL COUNT INCREASED ( 2 FDA reports)
ABNORMAL CHEST SOUND ( 1 FDA reports)
ADRENAL INSUFFICIENCY ( 1 FDA reports)
AFFECT LABILITY ( 1 FDA reports)
AGGRESSION ( 1 FDA reports)
AGITATION ( 1 FDA reports)
ALOPECIA ( 1 FDA reports)
ANAPHYLACTIC SHOCK ( 1 FDA reports)
ANGINA UNSTABLE ( 1 FDA reports)
APPETITE DISORDER ( 1 FDA reports)
ASTHMA ( 1 FDA reports)
BACK INJURY ( 1 FDA reports)
BACTERAEMIA ( 1 FDA reports)
BIPOLAR I DISORDER ( 1 FDA reports)
BLISTER ( 1 FDA reports)
BLOOD BILIRUBIN INCREASED ( 1 FDA reports)
BLOOD CHLORIDE DECREASED ( 1 FDA reports)
BLOOD CREATININE INCREASED ( 1 FDA reports)
BLOOD CULTURE POSITIVE ( 1 FDA reports)
BLOOD GLUCOSE INCREASED ( 1 FDA reports)
BLOOD OSMOLARITY DECREASED ( 1 FDA reports)
BLOOD UREA INCREASED ( 1 FDA reports)
BODY TEMPERATURE DECREASED ( 1 FDA reports)
CACHEXIA ( 1 FDA reports)
CALCULUS URETERIC ( 1 FDA reports)
CARDIO-RESPIRATORY ARREST ( 1 FDA reports)
CELLULITIS ( 1 FDA reports)
CHRONIC INFLAMMATORY DEMYELINATING POLYRADICULONEUROPATHY ( 1 FDA reports)
COLONY STIMULATING FACTOR THERAPY ( 1 FDA reports)
DIABETES MELLITUS INADEQUATE CONTROL ( 1 FDA reports)
DISUSE SYNDROME ( 1 FDA reports)
DIVERTICULITIS ( 1 FDA reports)
DRUG ERUPTION ( 1 FDA reports)
DRUG LEVEL INCREASED ( 1 FDA reports)
DYSSTASIA ( 1 FDA reports)
EMPHYSEMA ( 1 FDA reports)
ENTEROCOLITIS ( 1 FDA reports)
ESSENTIAL THROMBOCYTHAEMIA ( 1 FDA reports)
FEELING ABNORMAL ( 1 FDA reports)
FLUSHING ( 1 FDA reports)
GASTROENTERITIS VIRAL ( 1 FDA reports)
GRANULOCYTOPENIA ( 1 FDA reports)
GRANULOCYTOSIS ( 1 FDA reports)
HAEMATOCRIT DECREASED ( 1 FDA reports)
HAEMORRHAGE ( 1 FDA reports)
HEAD INJURY ( 1 FDA reports)
HEART RATE INCREASED ( 1 FDA reports)
HEAT RASH ( 1 FDA reports)
HEPATIC FAILURE ( 1 FDA reports)
HERPES ZOSTER ( 1 FDA reports)
HISTIOCYTOSIS HAEMATOPHAGIC ( 1 FDA reports)
HYDRONEPHROSIS ( 1 FDA reports)
HYPERCAPNIA ( 1 FDA reports)
HYPERKALAEMIA ( 1 FDA reports)
HYPOAESTHESIA ( 1 FDA reports)
HYPOALBUMINAEMIA ( 1 FDA reports)
HYPOGLYCAEMIC COMA ( 1 FDA reports)
HYPOTENSION ( 1 FDA reports)
INFECTION SUSCEPTIBILITY INCREASED ( 1 FDA reports)
INTERNATIONAL NORMALISED RATIO INCREASED ( 1 FDA reports)
JOINT DISLOCATION ( 1 FDA reports)
LABORATORY TEST INTERFERENCE ( 1 FDA reports)
LOCALISED OEDEMA ( 1 FDA reports)
METASTASES TO BLADDER ( 1 FDA reports)
METASTASES TO LIVER ( 1 FDA reports)
METASTASES TO NECK ( 1 FDA reports)
METASTASES TO UTERUS ( 1 FDA reports)
MICTURITION FREQUENCY DECREASED ( 1 FDA reports)
MYCOPLASMA INFECTION ( 1 FDA reports)
MYOCARDIAL INFARCTION ( 1 FDA reports)
NEPHRITIS ( 1 FDA reports)
NERVOUSNESS ( 1 FDA reports)
NEUROENDOCRINE CARCINOMA ( 1 FDA reports)
NEUROLEPTIC MALIGNANT SYNDROME ( 1 FDA reports)
NEUTROPHIL PERCENTAGE INCREASED ( 1 FDA reports)
NOCTURNAL DYSPNOEA ( 1 FDA reports)
NON-SMALL CELL LUNG CANCER ( 1 FDA reports)
NON-SMALL CELL LUNG CANCER METASTATIC ( 1 FDA reports)
OBESITY ( 1 FDA reports)
OEDEMA GENITAL ( 1 FDA reports)
OSTEOARTHRITIS ( 1 FDA reports)
OSTEONECROSIS OF JAW ( 1 FDA reports)
OVARIAN CANCER ( 1 FDA reports)
PAIN IN EXTREMITY ( 1 FDA reports)
PANCREATIC CARCINOMA ( 1 FDA reports)
PERITONEAL HAEMORRHAGE ( 1 FDA reports)
PLATELET TRANSFUSION ( 1 FDA reports)
PNEUMONIA STAPHYLOCOCCAL ( 1 FDA reports)
PNEUMOTHORAX ( 1 FDA reports)
PO2 DECREASED ( 1 FDA reports)
PRODUCTIVE COUGH ( 1 FDA reports)
PUPILLARY REFLEX IMPAIRED ( 1 FDA reports)
PYELONEPHRITIS ACUTE ( 1 FDA reports)
RASH GENERALISED ( 1 FDA reports)
RED BLOOD CELL COUNT DECREASED ( 1 FDA reports)
RENAL VASCULITIS ( 1 FDA reports)
RESPIRATORY RATE DECREASED ( 1 FDA reports)
RESPIRATORY TRACT INFECTION ( 1 FDA reports)
RHEUMATOID ARTHRITIS ( 1 FDA reports)
SKIN CHAPPED ( 1 FDA reports)
SPINAL COMPRESSION FRACTURE ( 1 FDA reports)
STEVENS-JOHNSON SYNDROME ( 1 FDA reports)
SYSTEMIC INFLAMMATORY RESPONSE SYNDROME ( 1 FDA reports)
THIRST ( 1 FDA reports)
TUBERCULOSIS ( 1 FDA reports)
URINARY RETENTION ( 1 FDA reports)
VASCULITIS ( 1 FDA reports)
WEIGHT DECREASED ( 1 FDA reports)
WEIGHT INCREASED ( 1 FDA reports)

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