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

HYPERTENSION ( 11 FDA reports)
MALAISE ( 10 FDA reports)
CEREBROVASCULAR ACCIDENT ( 9 FDA reports)
DRUG INEFFECTIVE ( 9 FDA reports)
PAIN ( 9 FDA reports)
DRY THROAT ( 7 FDA reports)
LYMPHATIC OBSTRUCTION ( 7 FDA reports)
PAIN IN EXTREMITY ( 7 FDA reports)
AGITATION ( 5 FDA reports)
JOINT RANGE OF MOTION DECREASED ( 5 FDA reports)
VISION BLURRED ( 5 FDA reports)
WEIGHT INCREASED ( 5 FDA reports)
BLOOD CREATINE PHOSPHOKINASE INCREASED ( 4 FDA reports)
BLOOD GLUCOSE FLUCTUATION ( 4 FDA reports)
BLOOD PRESSURE INCREASED ( 4 FDA reports)
BLOOD THYROID STIMULATING HORMONE ABNORMAL ( 4 FDA reports)
CEREBRAL ISCHAEMIA ( 4 FDA reports)
DIABETIC COMA ( 4 FDA reports)
DIZZINESS ( 4 FDA reports)
DYSPNOEA ( 4 FDA reports)
HEADACHE ( 4 FDA reports)
HYPERGLYCAEMIA ( 4 FDA reports)
MUSCULAR WEAKNESS ( 4 FDA reports)
OSTEOPENIA ( 4 FDA reports)
QUADRIPLEGIA ( 4 FDA reports)
SOMNOLENCE ( 4 FDA reports)
SPEECH DISORDER ( 4 FDA reports)
BEDRIDDEN ( 3 FDA reports)
BLISTER ( 3 FDA reports)
BLOOD PRESSURE DECREASED ( 3 FDA reports)
BURNING SENSATION ( 3 FDA reports)
CARDIAC DISORDER ( 3 FDA reports)
DIABETES MELLITUS ( 3 FDA reports)
FATIGUE ( 3 FDA reports)
FEELING ABNORMAL ( 3 FDA reports)
HALLUCINATION ( 3 FDA reports)
MULTI-ORGAN FAILURE ( 3 FDA reports)
NAUSEA ( 3 FDA reports)
PRESYNCOPE ( 3 FDA reports)
RENAL DISORDER ( 3 FDA reports)
SUICIDAL IDEATION ( 3 FDA reports)
TREMOR ( 3 FDA reports)
VOMITING ( 3 FDA reports)
WEIGHT LOSS POOR ( 3 FDA reports)
ADVERSE REACTION ( 2 FDA reports)
ANAEMIA ( 2 FDA reports)
APPLICATION SITE BLEEDING ( 2 FDA reports)
APPLICATION SITE ERYTHEMA ( 2 FDA reports)
APPLICATION SITE IRRITATION ( 2 FDA reports)
APPLICATION SITE PRURITUS ( 2 FDA reports)
ASTHENIA ( 2 FDA reports)
C-REACTIVE PROTEIN INCREASED ( 2 FDA reports)
CHEST DISCOMFORT ( 2 FDA reports)
COMA ( 2 FDA reports)
CONDITION AGGRAVATED ( 2 FDA reports)
CORONARY ARTERY OCCLUSION ( 2 FDA reports)
DIARRHOEA ( 2 FDA reports)
EATING DISORDER ( 2 FDA reports)
EMPHYSEMA ( 2 FDA reports)
FALL ( 2 FDA reports)
FOREARM FRACTURE ( 2 FDA reports)
GASTROENTERITIS ( 2 FDA reports)
GENERAL PHYSICAL HEALTH DETERIORATION ( 2 FDA reports)
IRRITABILITY ( 2 FDA reports)
NERVOUSNESS ( 2 FDA reports)
NO THERAPEUTIC RESPONSE ( 2 FDA reports)
OEDEMA PERIPHERAL ( 2 FDA reports)
PNEUMONIA ( 2 FDA reports)
RHEUMATOID ARTHRITIS ( 2 FDA reports)
SLEEP DISORDER ( 2 FDA reports)
THROMBOSIS ( 2 FDA reports)
UNEVALUABLE EVENT ( 2 FDA reports)
VISUAL IMPAIRMENT ( 2 FDA reports)
WRONG TECHNIQUE IN DRUG USAGE PROCESS ( 2 FDA reports)
ABDOMINAL ADHESIONS ( 1 FDA reports)
ABDOMINAL PAIN ( 1 FDA reports)
ANXIETY ( 1 FDA reports)
ARTERIAL THROMBOSIS LIMB ( 1 FDA reports)
ARTHROPATHY ( 1 FDA reports)
BLINDNESS ( 1 FDA reports)
BLOOD CREATININE INCREASED ( 1 FDA reports)
BLOOD POTASSIUM INCREASED ( 1 FDA reports)
BLOOD PRESSURE ABNORMAL ( 1 FDA reports)
BLOOD UREA INCREASED ( 1 FDA reports)
BRONCHITIS ( 1 FDA reports)
CARDIAC PACEMAKER INSERTION ( 1 FDA reports)
CHEST PAIN ( 1 FDA reports)
CONSTIPATION ( 1 FDA reports)
CORONARY ARTERY DISEASE ( 1 FDA reports)
COUGH ( 1 FDA reports)
CRYING ( 1 FDA reports)
DECREASED APPETITE ( 1 FDA reports)
DEHYDRATION ( 1 FDA reports)
DEPRESSED MOOD ( 1 FDA reports)
DEPRESSION ( 1 FDA reports)
DIPLOPIA ( 1 FDA reports)
DRUG ADMINISTRATION ERROR ( 1 FDA reports)
EPISTAXIS ( 1 FDA reports)
EXPIRED DRUG ADMINISTERED ( 1 FDA reports)
EYE HAEMORRHAGE ( 1 FDA reports)
FOETAL DEATH ( 1 FDA reports)
FOETAL EXPOSURE TIMING UNSPECIFIED ( 1 FDA reports)
FOOD POISONING ( 1 FDA reports)
GAIT DISTURBANCE ( 1 FDA reports)
GASTROINTESTINAL NECROSIS ( 1 FDA reports)
HAEMODIALYSIS ( 1 FDA reports)
HEART INJURY ( 1 FDA reports)
HERPES ZOSTER OPHTHALMIC ( 1 FDA reports)
HYPERHIDROSIS ( 1 FDA reports)
HYPERSENSITIVITY ( 1 FDA reports)
HYPOGLYCAEMIA ( 1 FDA reports)
INFARCTION ( 1 FDA reports)
INFLUENZA ( 1 FDA reports)
INJECTION SITE DISCOLOURATION ( 1 FDA reports)
INJECTION SITE HAEMATOMA ( 1 FDA reports)
INJECTION SITE NODULE ( 1 FDA reports)
INJECTION SITE PAIN ( 1 FDA reports)
INJECTION SITE REACTION ( 1 FDA reports)
INJECTION SITE SWELLING ( 1 FDA reports)
INSOMNIA ( 1 FDA reports)
ISCHAEMIA ( 1 FDA reports)
LABYRINTHITIS ( 1 FDA reports)
LOSS OF CONSCIOUSNESS ( 1 FDA reports)
MEMORY IMPAIRMENT ( 1 FDA reports)
MENTAL DISORDER ( 1 FDA reports)
MICTURITION URGENCY ( 1 FDA reports)
MULTIPLE SCLEROSIS RELAPSE ( 1 FDA reports)
MUSCLE SPASMS ( 1 FDA reports)
MYALGIA ( 1 FDA reports)
MYOCARDIAL INFARCTION ( 1 FDA reports)
NASOPHARYNGITIS ( 1 FDA reports)
NECROSIS ( 1 FDA reports)
PALPITATIONS ( 1 FDA reports)
PRURITUS ( 1 FDA reports)
RASH MACULAR ( 1 FDA reports)
RENAL IMPAIRMENT ( 1 FDA reports)
RESPIRATORY FAILURE ( 1 FDA reports)
RESTLESSNESS ( 1 FDA reports)
RETINAL INJURY ( 1 FDA reports)
SALIVARY HYPERSECRETION ( 1 FDA reports)
SCAB ( 1 FDA reports)
SKIN INFECTION ( 1 FDA reports)
SPINAL FRACTURE ( 1 FDA reports)
URINARY TRACT INFECTION ( 1 FDA reports)
URINE ODOUR ABNORMAL ( 1 FDA reports)
UTERINE CANCER ( 1 FDA reports)
VERTIGO ( 1 FDA reports)
VISUAL ACUITY REDUCED ( 1 FDA reports)
VITREOUS FLOATERS ( 1 FDA reports)
WALKING DISABILITY ( 1 FDA reports)
WEIGHT DECREASED ( 1 FDA reports)
WHEEZING ( 1 FDA reports)

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