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

CHEST PAIN ( 15 FDA reports)
MULTIPLE FRACTURES ( 15 FDA reports)
BLOOD ALKALINE PHOSPHATASE INCREASED ( 12 FDA reports)
OSTEOMALACIA ( 10 FDA reports)
PRURITUS ( 7 FDA reports)
DRUG ERUPTION ( 5 FDA reports)
PYREXIA ( 5 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 4 FDA reports)
TREMOR ( 4 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 3 FDA reports)
BACK PAIN ( 3 FDA reports)
BLUNTED AFFECT ( 3 FDA reports)
HEADACHE ( 3 FDA reports)
HEPATIC FUNCTION ABNORMAL ( 3 FDA reports)
LIVER DISORDER ( 3 FDA reports)
SOMNOLENCE ( 3 FDA reports)
ARTHRALGIA ( 2 FDA reports)
BACTERAEMIA ( 2 FDA reports)
BLOOD CREATININE INCREASED ( 2 FDA reports)
BLOOD UREA INCREASED ( 2 FDA reports)
CHEST DISCOMFORT ( 2 FDA reports)
CHILLS ( 2 FDA reports)
EXTRASYSTOLES ( 2 FDA reports)
HAEMATURIA ( 2 FDA reports)
LUNG DISORDER ( 2 FDA reports)
NAUSEA ( 2 FDA reports)
PALPITATIONS ( 2 FDA reports)
PANCYTOPENIA ( 2 FDA reports)
THROMBOCYTOPENIA ( 2 FDA reports)
URINARY RETENTION ( 2 FDA reports)
ABDOMINAL TENDERNESS ( 1 FDA reports)
AMINOACIDURIA ( 1 FDA reports)
APHTHOUS STOMATITIS ( 1 FDA reports)
ARTERIOSCLEROSIS ( 1 FDA reports)
ASPARTATE AMINOTRANSFERASE ( 1 FDA reports)
ASTHENIA ( 1 FDA reports)
BILIRUBIN CONJUGATED INCREASED ( 1 FDA reports)
BLOOD BILIRUBIN INCREASED ( 1 FDA reports)
BLOOD LACTATE DEHYDROGENASE INCREASED ( 1 FDA reports)
BURNING SENSATION ( 1 FDA reports)
CHRONIC FATIGUE SYNDROME ( 1 FDA reports)
COLD SWEAT ( 1 FDA reports)
CONDITION AGGRAVATED ( 1 FDA reports)
CONVULSION ( 1 FDA reports)
CRYING ( 1 FDA reports)
CYANOSIS ( 1 FDA reports)
DEPRESSED MOOD ( 1 FDA reports)
DIABETES MELLITUS ( 1 FDA reports)
DIARRHOEA ( 1 FDA reports)
DIZZINESS ( 1 FDA reports)
DIZZINESS POSTURAL ( 1 FDA reports)
DRUG INTERACTION ( 1 FDA reports)
DYSKINESIA ( 1 FDA reports)
DYSPNOEA ( 1 FDA reports)
ECONOMIC PROBLEM ( 1 FDA reports)
EMOTIONAL DISORDER ( 1 FDA reports)
EXTRAPYRAMIDAL DISORDER ( 1 FDA reports)
FANCONI SYNDROME ( 1 FDA reports)
FATIGUE ( 1 FDA reports)
FONTANELLE DEPRESSED ( 1 FDA reports)
GAIT DISTURBANCE ( 1 FDA reports)
GASTRITIS ( 1 FDA reports)
GASTROOESOPHAGEAL REFLUX DISEASE ( 1 FDA reports)
GLOSSODYNIA ( 1 FDA reports)
GRIEF REACTION ( 1 FDA reports)
HAEMATOCHEZIA ( 1 FDA reports)
HYPERPHOSPHATASAEMIA ( 1 FDA reports)
HYPOAESTHESIA ( 1 FDA reports)
HYPOPNOEA ( 1 FDA reports)
HYPOVOLAEMIA ( 1 FDA reports)
INJECTION SITE ERYTHEMA ( 1 FDA reports)
INJECTION SITE INDURATION ( 1 FDA reports)
INJECTION SITE PAIN ( 1 FDA reports)
INJECTION SITE SWELLING ( 1 FDA reports)
INJURY ( 1 FDA reports)
INSOMNIA ( 1 FDA reports)
INTERSTITIAL LUNG DISEASE ( 1 FDA reports)
INTERVERTEBRAL DISC DISORDER ( 1 FDA reports)
JAUNDICE ( 1 FDA reports)
LEUKOCYTOSIS ( 1 FDA reports)
LOSS OF CONSCIOUSNESS ( 1 FDA reports)
LYMPHADENOPATHY ( 1 FDA reports)
MELAENA ( 1 FDA reports)
MUSCLE SPASMS ( 1 FDA reports)
MUSCULAR WEAKNESS ( 1 FDA reports)
OBESITY ( 1 FDA reports)
PAIN IN EXTREMITY ( 1 FDA reports)
PALLOR ( 1 FDA reports)
PARAESTHESIA ( 1 FDA reports)
PERICARDIAL EFFUSION ( 1 FDA reports)
PLEURISY ( 1 FDA reports)
POLYARTERITIS NODOSA ( 1 FDA reports)
PULSE PRESSURE DECREASED ( 1 FDA reports)
RASH ( 1 FDA reports)
RECTAL ULCER ( 1 FDA reports)
RENAL DISORDER ( 1 FDA reports)
RESPIRATORY ARREST ( 1 FDA reports)
SLEEP DISORDER ( 1 FDA reports)
SNORING ( 1 FDA reports)
SPINAL OSTEOARTHRITIS ( 1 FDA reports)
STRESS ( 1 FDA reports)
SYNCOPE ( 1 FDA reports)
TARDIVE DYSKINESIA ( 1 FDA reports)
TEMPERATURE INTOLERANCE ( 1 FDA reports)
TONGUE DISORDER ( 1 FDA reports)
URINE PHOSPHORUS INCREASED ( 1 FDA reports)
YELLOW SKIN ( 1 FDA reports)

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