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

DYSPNOEA ( 9 FDA reports)
FATIGUE ( 8 FDA reports)
NAUSEA ( 7 FDA reports)
SYNCOPE ( 7 FDA reports)
ANAEMIA ( 6 FDA reports)
CEREBROVASCULAR ACCIDENT ( 6 FDA reports)
CONTUSION ( 5 FDA reports)
DIZZINESS ( 5 FDA reports)
GASTROINTESTINAL HAEMORRHAGE ( 5 FDA reports)
HEADACHE ( 5 FDA reports)
OCULAR DISCOMFORT ( 5 FDA reports)
RHEUMATOID ARTHRITIS ( 5 FDA reports)
TACHYCARDIA ( 5 FDA reports)
TRANSFUSION ( 5 FDA reports)
BLINDNESS ( 4 FDA reports)
DRUG INEFFECTIVE ( 4 FDA reports)
HAEMORRHAGE ( 4 FDA reports)
HYPOTENSION ( 4 FDA reports)
RENAL FAILURE ( 4 FDA reports)
SPEECH DISORDER ( 4 FDA reports)
ANXIETY ( 3 FDA reports)
ASTHENIA ( 3 FDA reports)
BLOOD GLUCOSE INCREASED ( 3 FDA reports)
BRADYCARDIA ( 3 FDA reports)
CARDIAC FAILURE ( 3 FDA reports)
COLD SWEAT ( 3 FDA reports)
DEAFNESS ( 3 FDA reports)
ERYTHEMA ( 3 FDA reports)
FEELING HOT ( 3 FDA reports)
GAIT DISTURBANCE ( 3 FDA reports)
HYPERHIDROSIS ( 3 FDA reports)
OEDEMA PERIPHERAL ( 3 FDA reports)
PAIN ( 3 FDA reports)
VERTEBROPLASTY ( 3 FDA reports)
ABDOMINAL PAIN UPPER ( 2 FDA reports)
ABNORMAL LOSS OF WEIGHT ( 2 FDA reports)
ANGIOEDEMA ( 2 FDA reports)
ARTHRALGIA ( 2 FDA reports)
ARTHRITIS ( 2 FDA reports)
BLOOD UREA INCREASED ( 2 FDA reports)
CARDIOGENIC SHOCK ( 2 FDA reports)
CHEST PAIN ( 2 FDA reports)
CULTURE URINE POSITIVE ( 2 FDA reports)
DEATH ( 2 FDA reports)
DIARRHOEA HAEMORRHAGIC ( 2 FDA reports)
EAR DISORDER ( 2 FDA reports)
ESCHERICHIA INFECTION ( 2 FDA reports)
EYE PRURITUS ( 2 FDA reports)
FEELING ABNORMAL ( 2 FDA reports)
GASTROOESOPHAGEAL REFLUX DISEASE ( 2 FDA reports)
GLOMERULAR FILTRATION RATE DECREASED ( 2 FDA reports)
HEART RATE INCREASED ( 2 FDA reports)
HYPOACUSIS ( 2 FDA reports)
INJURY ( 2 FDA reports)
INSOMNIA ( 2 FDA reports)
ISCHAEMIC HEPATITIS ( 2 FDA reports)
KYPHOSIS ( 2 FDA reports)
LYMPHOCYTE COUNT DECREASED ( 2 FDA reports)
LYMPHOCYTE PERCENTAGE DECREASED ( 2 FDA reports)
MEDICATION ERROR ( 2 FDA reports)
NASAL INFLAMMATION ( 2 FDA reports)
NEPHROGENIC ANAEMIA ( 2 FDA reports)
NEURALGIA ( 2 FDA reports)
NEUTROPHIL COUNT INCREASED ( 2 FDA reports)
OXYGEN SATURATION DECREASED ( 2 FDA reports)
PAIN IN EXTREMITY ( 2 FDA reports)
PALPITATIONS ( 2 FDA reports)
PANIC ATTACK ( 2 FDA reports)
POOR QUALITY SLEEP ( 2 FDA reports)
PROTEIN TOTAL DECREASED ( 2 FDA reports)
PYELONEPHRITIS ( 2 FDA reports)
RETROPERITONEAL HAEMATOMA ( 2 FDA reports)
STOMATITIS ( 2 FDA reports)
STRESS ( 2 FDA reports)
VERTIGO ( 2 FDA reports)
VISION BLURRED ( 2 FDA reports)
VISUAL IMPAIRMENT ( 2 FDA reports)
VOMITING ( 2 FDA reports)
WEIGHT DECREASED ( 2 FDA reports)
WHITE BLOOD CELL COUNT INCREASED ( 2 FDA reports)
ABASIA ( 1 FDA reports)
ACUTE MYOCARDIAL INFARCTION ( 1 FDA reports)
ALOPECIA ( 1 FDA reports)
ANGIOPATHY ( 1 FDA reports)
APPLICATION SITE BURN ( 1 FDA reports)
APPLICATION SITE DISCOLOURATION ( 1 FDA reports)
APPLICATION SITE PAIN ( 1 FDA reports)
APPLICATION SITE SCAR ( 1 FDA reports)
APPLICATION SITE VESICLES ( 1 FDA reports)
ATRIAL FIBRILLATION ( 1 FDA reports)
BACK PAIN ( 1 FDA reports)
BALANCE DISORDER ( 1 FDA reports)
BLADDER DISORDER ( 1 FDA reports)
BLISTER ( 1 FDA reports)
BLOOD CALCIUM DECREASED ( 1 FDA reports)
BLOOD POTASSIUM DECREASED ( 1 FDA reports)
BLOOD PRESSURE DECREASED ( 1 FDA reports)
BLOOD URINE PRESENT ( 1 FDA reports)
BODY TEMPERATURE INCREASED ( 1 FDA reports)
BONE PAIN ( 1 FDA reports)
BURNING SENSATION ( 1 FDA reports)
BURNS SECOND DEGREE ( 1 FDA reports)
CALCIUM IONISED DECREASED ( 1 FDA reports)
CARBON DIOXIDE DECREASED ( 1 FDA reports)
CARDIAC ARREST ( 1 FDA reports)
CARDIOMEGALY ( 1 FDA reports)
CARDIOVASCULAR DISORDER ( 1 FDA reports)
CAROTID ARTERY ATHEROMA ( 1 FDA reports)
CEREBRAL ISCHAEMIA ( 1 FDA reports)
CHROMATURIA ( 1 FDA reports)
CORONARY ARTERY OCCLUSION ( 1 FDA reports)
COUGH ( 1 FDA reports)
DELUSIONAL DISORDER, UNSPECIFIED TYPE ( 1 FDA reports)
DEPRESSED LEVEL OF CONSCIOUSNESS ( 1 FDA reports)
DIARRHOEA ( 1 FDA reports)
DILATATION ATRIAL ( 1 FDA reports)
DRUG DISPENSING ERROR ( 1 FDA reports)
DRUG TOXICITY ( 1 FDA reports)
DYSPEPSIA ( 1 FDA reports)
EAR PAIN ( 1 FDA reports)
EPISTAXIS ( 1 FDA reports)
EYE IRRITATION ( 1 FDA reports)
FALL ( 1 FDA reports)
FLUSHING ( 1 FDA reports)
FOREIGN BODY ( 1 FDA reports)
GASTROINTESTINAL TRACT IRRITATION ( 1 FDA reports)
HAEMATOCHEZIA ( 1 FDA reports)
HAEMOGLOBIN DECREASED ( 1 FDA reports)
HAEMOPTYSIS ( 1 FDA reports)
HEPATIC ENCEPHALOPATHY ( 1 FDA reports)
HEPATIC FIBROSIS ( 1 FDA reports)
HEPATITIS C ( 1 FDA reports)
HYPOAESTHESIA ( 1 FDA reports)
HYPOGLYCAEMIA ( 1 FDA reports)
INCOHERENT ( 1 FDA reports)
INCREASED UPPER AIRWAY SECRETION ( 1 FDA reports)
INTERVERTEBRAL DISC DISORDER ( 1 FDA reports)
LACRIMATION INCREASED ( 1 FDA reports)
LIVER DISORDER ( 1 FDA reports)
LIVER INJURY ( 1 FDA reports)
MICTURITION URGENCY ( 1 FDA reports)
MUSCLE SPASMS ( 1 FDA reports)
MUSCULOSKELETAL PAIN ( 1 FDA reports)
MYALGIA ( 1 FDA reports)
MYOCARDIAL INFARCTION ( 1 FDA reports)
NO ADVERSE EVENT ( 1 FDA reports)
OCULAR HYPERAEMIA ( 1 FDA reports)
OESOPHAGEAL IRRITATION ( 1 FDA reports)
OROPHARYNGEAL PAIN ( 1 FDA reports)
OSTEITIS ( 1 FDA reports)
OSTEOPOROSIS ( 1 FDA reports)
PAIN IN JAW ( 1 FDA reports)
PHARMACEUTICAL PRODUCT COMPLAINT ( 1 FDA reports)
PRURITUS ( 1 FDA reports)
PYREXIA ( 1 FDA reports)
RASH MACULAR ( 1 FDA reports)
READING DISORDER ( 1 FDA reports)
RECTAL HAEMORRHAGE ( 1 FDA reports)
RED BLOOD CELL COUNT DECREASED ( 1 FDA reports)
REGURGITATION ( 1 FDA reports)
RHINORRHOEA ( 1 FDA reports)
SCAB ( 1 FDA reports)
SENSATION OF FOREIGN BODY ( 1 FDA reports)
SINUS BRADYCARDIA ( 1 FDA reports)
TONGUE COATED ( 1 FDA reports)
TONGUE DISORDER ( 1 FDA reports)
URINARY RETENTION ( 1 FDA reports)
VENTRICULAR HYPERTROPHY ( 1 FDA reports)

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