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

DIARRHOEA ( 9 FDA reports)
DRUG INTERACTION ( 9 FDA reports)
CONVULSION ( 7 FDA reports)
DYSPNOEA ( 7 FDA reports)
NAUSEA ( 7 FDA reports)
DIZZINESS ( 6 FDA reports)
OSTEONECROSIS ( 6 FDA reports)
ARTERIAL THROMBOSIS ( 5 FDA reports)
BLOOD PRESSURE DECREASED ( 5 FDA reports)
FALL ( 5 FDA reports)
IMPAIRED HEALING ( 5 FDA reports)
INSOMNIA ( 5 FDA reports)
NEUTROPENIA ( 5 FDA reports)
TOOTH EXTRACTION ( 5 FDA reports)
BONE DISORDER ( 4 FDA reports)
CARDIAC DISORDER ( 4 FDA reports)
CONDITION AGGRAVATED ( 4 FDA reports)
DRUG LEVEL BELOW THERAPEUTIC ( 4 FDA reports)
DYSPNOEA EXERTIONAL ( 4 FDA reports)
FLUID RETENTION ( 4 FDA reports)
GASTROINTESTINAL HAEMORRHAGE ( 4 FDA reports)
GASTROINTESTINAL PAIN ( 4 FDA reports)
HYPERTENSION ( 4 FDA reports)
LEUKOPENIA ( 4 FDA reports)
METASTATIC SQUAMOUS CELL CARCINOMA ( 4 FDA reports)
PAIN ( 4 FDA reports)
PAIN IN EXTREMITY ( 4 FDA reports)
RASH ( 4 FDA reports)
ANAEMIA ( 3 FDA reports)
BLOOD SODIUM DECREASED ( 3 FDA reports)
CAMPYLOBACTER INTESTINAL INFECTION ( 3 FDA reports)
COLLAPSE OF LUNG ( 3 FDA reports)
ERYTHEMA ( 3 FDA reports)
FATIGUE ( 3 FDA reports)
FEBRILE NEUTROPENIA ( 3 FDA reports)
HEART RATE DECREASED ( 3 FDA reports)
HYPOAESTHESIA ORAL ( 3 FDA reports)
HYPOXIA ( 3 FDA reports)
INTERSTITIAL LUNG DISEASE ( 3 FDA reports)
LIVER FUNCTION TEST ABNORMAL ( 3 FDA reports)
LOSS OF CONSCIOUSNESS ( 3 FDA reports)
OEDEMA ( 3 FDA reports)
PAIN IN JAW ( 3 FDA reports)
PNEUMONIA ( 3 FDA reports)
POLYNEUROPATHY ( 3 FDA reports)
PULMONARY CONGESTION ( 3 FDA reports)
PYREXIA ( 3 FDA reports)
TOOTH ABSCESS ( 3 FDA reports)
TOOTHACHE ( 3 FDA reports)
TRANSIENT ISCHAEMIC ATTACK ( 3 FDA reports)
VISUAL DISTURBANCE ( 3 FDA reports)
VOMITING ( 3 FDA reports)
WOUND DEBRIDEMENT ( 3 FDA reports)
YELLOW SKIN ( 3 FDA reports)
ABASIA ( 2 FDA reports)
ABDOMINAL PAIN UPPER ( 2 FDA reports)
ABNORMAL FAECES ( 2 FDA reports)
ANOREXIA ( 2 FDA reports)
ASTHENIA ( 2 FDA reports)
ASTHMA ( 2 FDA reports)
BALANCE DISORDER ( 2 FDA reports)
BLOOD CREATININE INCREASED ( 2 FDA reports)
CHEST PAIN ( 2 FDA reports)
CHOLELITHIASIS ( 2 FDA reports)
CONSTIPATION ( 2 FDA reports)
DEHYDRATION ( 2 FDA reports)
DRUG ADMINISTRATION ERROR ( 2 FDA reports)
DRUG HYPERSENSITIVITY ( 2 FDA reports)
DRUG LEVEL INCREASED ( 2 FDA reports)
DYSAESTHESIA ( 2 FDA reports)
FAECES DISCOLOURED ( 2 FDA reports)
FEMUR FRACTURE ( 2 FDA reports)
FLATULENCE ( 2 FDA reports)
HALLUCINATION ( 2 FDA reports)
HIP FRACTURE ( 2 FDA reports)
INFERTILITY ( 2 FDA reports)
LETHARGY ( 2 FDA reports)
LYMPHOMA ( 2 FDA reports)
MALAISE ( 2 FDA reports)
MUSCLE SPASMS ( 2 FDA reports)
MUSCULAR WEAKNESS ( 2 FDA reports)
OVERDOSE ( 2 FDA reports)
PLEURAL EFFUSION ( 2 FDA reports)
PNEUMOTHORAX ( 2 FDA reports)
RESPIRATORY DEPRESSION ( 2 FDA reports)
SEPSIS ( 2 FDA reports)
SOFT TISSUE INFECTION ( 2 FDA reports)
ACUTE MYOCARDIAL INFARCTION ( 1 FDA reports)
ACUTE PSYCHOSIS ( 1 FDA reports)
AGGRESSION ( 1 FDA reports)
ANHEDONIA ( 1 FDA reports)
ARRHYTHMIA ( 1 FDA reports)
ARTERIAL THROMBOSIS LIMB ( 1 FDA reports)
ARTHRALGIA ( 1 FDA reports)
ARTHROPATHY ( 1 FDA reports)
ATRIAL FIBRILLATION ( 1 FDA reports)
ATRIAL TACHYCARDIA ( 1 FDA reports)
BACK PAIN ( 1 FDA reports)
BLISTER ( 1 FDA reports)
BLOOD ALBUMIN DECREASED ( 1 FDA reports)
BLOOD PARATHYROID HORMONE INCREASED ( 1 FDA reports)
BLOOD POTASSIUM DECREASED ( 1 FDA reports)
BLOOD PRESSURE INCREASED ( 1 FDA reports)
BONE SCAN ABNORMAL ( 1 FDA reports)
C-REACTIVE PROTEIN INCREASED ( 1 FDA reports)
CARDIAC ARREST ( 1 FDA reports)
CARDIAC FAILURE CONGESTIVE ( 1 FDA reports)
CEREBROVASCULAR ACCIDENT ( 1 FDA reports)
CHILLS ( 1 FDA reports)
COLD SWEAT ( 1 FDA reports)
COLITIS ( 1 FDA reports)
CONFUSIONAL STATE ( 1 FDA reports)
COUGH ( 1 FDA reports)
DEATH ( 1 FDA reports)
DECREASED APPETITE ( 1 FDA reports)
DENTAL CARIES ( 1 FDA reports)
DIFFICULTY IN WALKING ( 1 FDA reports)
DISEASE PROGRESSION ( 1 FDA reports)
DRUG ABUSE ( 1 FDA reports)
DRUG INEFFECTIVE ( 1 FDA reports)
DRY SOCKET ( 1 FDA reports)
DYSLIPIDAEMIA ( 1 FDA reports)
EPISTAXIS ( 1 FDA reports)
ESCHERICHIA TEST POSITIVE ( 1 FDA reports)
FAT TISSUE INCREASED ( 1 FDA reports)
FEMORAL ARTERY OCCLUSION ( 1 FDA reports)
GAMMA-GLUTAMYLTRANSFERASE INCREASED ( 1 FDA reports)
GINGIVAL SWELLING ( 1 FDA reports)
HAEMATOCHEZIA ( 1 FDA reports)
HAEMOGLOBIN DECREASED ( 1 FDA reports)
HAEMORRHAGE ( 1 FDA reports)
HEPATIC FUNCTION ABNORMAL ( 1 FDA reports)
HERPES ZOSTER ( 1 FDA reports)
HYPERSENSITIVITY ( 1 FDA reports)
HYPOCHLORAEMIA ( 1 FDA reports)
HYPONATRAEMIA ( 1 FDA reports)
HYPOTENSION ( 1 FDA reports)
HYPOVOLAEMIA ( 1 FDA reports)
INAPPROPRIATE ANTIDIURETIC HORMONE SECRETION ( 1 FDA reports)
INCORRECT DOSE ADMINISTERED ( 1 FDA reports)
INFLUENZA LIKE ILLNESS ( 1 FDA reports)
INFUSION SITE REACTION ( 1 FDA reports)
INJECTION SITE REACTION ( 1 FDA reports)
INTENTION TREMOR ( 1 FDA reports)
JAUNDICE ( 1 FDA reports)
JAW OPERATION ( 1 FDA reports)
LOWER RESPIRATORY TRACT INFECTION ( 1 FDA reports)
LUNG INFECTION ( 1 FDA reports)
MALIGNANT NEOPLASM PROGRESSION ( 1 FDA reports)
MENINGIOMA ( 1 FDA reports)
METASTASES TO CENTRAL NERVOUS SYSTEM ( 1 FDA reports)
MOOD SWINGS ( 1 FDA reports)
MUCOSAL ULCERATION ( 1 FDA reports)
NEOPLASM MALIGNANT ( 1 FDA reports)
NEOPLASM PROGRESSION ( 1 FDA reports)
NEUROSURGERY ( 1 FDA reports)
OEDEMA MUCOSAL ( 1 FDA reports)
ORTHOSTATIC HYPOTENSION ( 1 FDA reports)
OSTEOPENIA ( 1 FDA reports)
PANCREATITIS ACUTE ( 1 FDA reports)
PARAESTHESIA ( 1 FDA reports)
PARAESTHESIA ORAL ( 1 FDA reports)
PARANOIA ( 1 FDA reports)
PAROTITIS ( 1 FDA reports)
PERIPHERAL VASCULAR DISORDER ( 1 FDA reports)
PERITONITIS ( 1 FDA reports)
PRODUCTIVE COUGH ( 1 FDA reports)
PULMONARY EMBOLISM ( 1 FDA reports)
PURPURA ( 1 FDA reports)
RALES ( 1 FDA reports)
RASH MACULAR ( 1 FDA reports)
RED BLOOD CELL ABNORMALITY ( 1 FDA reports)
RED BLOOD CELL SEDIMENTATION RATE ABNORMAL ( 1 FDA reports)
RENAL FAILURE CHRONIC ( 1 FDA reports)
RENAL IMPAIRMENT ( 1 FDA reports)
RESPIRATION ABNORMAL ( 1 FDA reports)
RETINAL EXUDATES ( 1 FDA reports)
SJOGREN'S SYNDROME ( 1 FDA reports)
SKIN DISCOLOURATION ( 1 FDA reports)
SPERMATOZOA MORPHOLOGY ABNORMAL ( 1 FDA reports)
SPERMATOZOA PROGRESSIVE MOTILITY ABNORMAL ( 1 FDA reports)
SWELLING FACE ( 1 FDA reports)
SYNCOPE ( 1 FDA reports)
SYSTEMIC LUPUS ERYTHEMATOSUS ( 1 FDA reports)
TREMOR ( 1 FDA reports)
TYPE I HYPERSENSITIVITY ( 1 FDA reports)
VIOLENCE-RELATED SYMPTOM ( 1 FDA reports)
VITAMIN D DECREASED ( 1 FDA reports)
WEIGHT INCREASED ( 1 FDA reports)
WEIGHT LOSS DIET ( 1 FDA reports)
WHEEZING ( 1 FDA reports)

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