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

NAUSEA ( 5 FDA reports)
ASTHENIA ( 3 FDA reports)
BACK PAIN ( 2 FDA reports)
BLOOD GLUCOSE DECREASED ( 2 FDA reports)
CONDITION AGGRAVATED ( 2 FDA reports)
DIARRHOEA ( 2 FDA reports)
FALL ( 2 FDA reports)
FATIGUE ( 2 FDA reports)
FEELING ABNORMAL ( 2 FDA reports)
INFECTION ( 2 FDA reports)
MUSCLE CRAMP ( 2 FDA reports)
PYREXIA ( 2 FDA reports)
THYROID DISORDER ( 2 FDA reports)
VOMITING ( 2 FDA reports)
WEIGHT INCREASED ( 2 FDA reports)
ABORTION INDUCED ( 1 FDA reports)
ACUTE MYOCARDIAL INFARCTION ( 1 FDA reports)
ACUTE RESPIRATORY FAILURE ( 1 FDA reports)
ARTHRITIS INFECTIVE ( 1 FDA reports)
BACK INJURY ( 1 FDA reports)
BENIGN PROSTATIC HYPERPLASIA ( 1 FDA reports)
BLOOD CHLORIDE DECREASED ( 1 FDA reports)
BLOOD CHOLESTEROL INCREASED ( 1 FDA reports)
BLOOD CREATINE PHOSPHOKINASE INCREASED ( 1 FDA reports)
BLOOD IRON DECREASED ( 1 FDA reports)
BLOOD SODIUM DECREASED ( 1 FDA reports)
BONE PAIN ( 1 FDA reports)
BONE SCAN ABNORMAL ( 1 FDA reports)
CELLULITIS ( 1 FDA reports)
CHEST PAIN ( 1 FDA reports)
CHILLS ( 1 FDA reports)
CHRONIC OBSTRUCTIVE AIRWAYS DISEASE EXACERBATED ( 1 FDA reports)
COELIAC DISEASE ( 1 FDA reports)
CONFUSIONAL STATE ( 1 FDA reports)
CONTUSION ( 1 FDA reports)
DIABETES MELLITUS INADEQUATE CONTROL ( 1 FDA reports)
DRUG EXPOSURE DURING PREGNANCY ( 1 FDA reports)
ECTOPIC PREGNANCY ( 1 FDA reports)
FLUSHING ( 1 FDA reports)
GASTRIC DISORDER ( 1 FDA reports)
GASTROINTESTINAL HAEMORRHAGE ( 1 FDA reports)
HYPERTENSION ( 1 FDA reports)
HYPOGLYCAEMIA ( 1 FDA reports)
HYPOKINESIA ( 1 FDA reports)
HYPOTENSION ( 1 FDA reports)
IMPAIRED DRIVING ABILITY ( 1 FDA reports)
IMPAIRED GASTRIC EMPTYING ( 1 FDA reports)
IMPAIRED HEALING ( 1 FDA reports)
INFLAMMATION ( 1 FDA reports)
INFLUENZA ( 1 FDA reports)
INJECTION SITE HAEMORRHAGE ( 1 FDA reports)
INJECTION SITE PAIN ( 1 FDA reports)
INTERSTITIAL LUNG DISEASE ( 1 FDA reports)
INTERVERTEBRAL DISC COMPRESSION ( 1 FDA reports)
IRON DEFICIENCY ANAEMIA ( 1 FDA reports)
LOWER LIMB FRACTURE ( 1 FDA reports)
LUMBAR VERTEBRAL FRACTURE ( 1 FDA reports)
LUNG DISORDER ( 1 FDA reports)
LUNG INFILTRATION ( 1 FDA reports)
MOVEMENT DISORDER ( 1 FDA reports)
MULTIPLE FRACTURES ( 1 FDA reports)
MUSCLE RUPTURE ( 1 FDA reports)
MYOCARDIAL INFARCTION ( 1 FDA reports)
NASOPHARYNGITIS ( 1 FDA reports)
NEUTROPHIL COUNT DECREASED ( 1 FDA reports)
OBLITERATIVE BRONCHIOLITIS ( 1 FDA reports)
ORTHOSTATIC HYPOTENSION ( 1 FDA reports)
OSTEOPOROSIS ( 1 FDA reports)
OVERDOSE ( 1 FDA reports)
PCO2 INCREASED ( 1 FDA reports)
PELVIC FRACTURE ( 1 FDA reports)
PHARMACEUTICAL PRODUCT COMPLAINT ( 1 FDA reports)
PITTING OEDEMA ( 1 FDA reports)
PLEURAL EFFUSION ( 1 FDA reports)
PNEUMONITIS ( 1 FDA reports)
PULMONARY FIBROSIS ( 1 FDA reports)
RASH ( 1 FDA reports)
RECTAL HAEMORRHAGE ( 1 FDA reports)
RENAL DISORDER ( 1 FDA reports)
RENAL FAILURE ( 1 FDA reports)
RESPIRATORY FAILURE ( 1 FDA reports)
RHEUMATOID ARTHRITIS ( 1 FDA reports)
RIB FRACTURE ( 1 FDA reports)
ROAD TRAFFIC ACCIDENT ( 1 FDA reports)
SCAR ( 1 FDA reports)
SKIN CANCER ( 1 FDA reports)
SKIN ULCER ( 1 FDA reports)
SOMNOLENCE ( 1 FDA reports)
SPINAL COMPRESSION FRACTURE ( 1 FDA reports)
SPINAL DISORDER ( 1 FDA reports)
STAPHYLOCOCCAL INFECTION ( 1 FDA reports)
STOMACH DISCOMFORT ( 1 FDA reports)
SUICIDE ATTEMPT ( 1 FDA reports)
SYNOVITIS ( 1 FDA reports)
THERMAL BURN ( 1 FDA reports)
TOOTH INFECTION ( 1 FDA reports)
TOOTHACHE ( 1 FDA reports)
TREMOR ( 1 FDA reports)
TUMOUR ASSOCIATED FEVER ( 1 FDA reports)
URINARY INCONTINENCE ( 1 FDA reports)
URINARY RETENTION ( 1 FDA reports)
VIRAL INFECTION ( 1 FDA reports)
WHITE BLOOD CELL COUNT DECREASED ( 1 FDA reports)
WHITE BLOOD CELL COUNT INCREASED ( 1 FDA reports)

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