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

ANXIETY ( 6 FDA reports)
DIZZINESS ( 6 FDA reports)
DYSPNOEA ( 6 FDA reports)
DYSGEUSIA ( 5 FDA reports)
DYSPHAGIA ( 5 FDA reports)
LUNG NEOPLASM MALIGNANT ( 5 FDA reports)
ANOREXIA ( 4 FDA reports)
GAIT DISTURBANCE ( 4 FDA reports)
MALAISE ( 4 FDA reports)
ORAL INTAKE REDUCED ( 4 FDA reports)
SLEEP DISORDER ( 4 FDA reports)
WEIGHT DECREASED ( 4 FDA reports)
ABASIA ( 3 FDA reports)
ASTHMA ( 3 FDA reports)
ATRIAL FIBRILLATION ( 3 FDA reports)
CHEST DISCOMFORT ( 3 FDA reports)
CHEST PAIN ( 3 FDA reports)
DRUG HYPERSENSITIVITY ( 3 FDA reports)
PNEUMONIA ( 3 FDA reports)
CONDITION AGGRAVATED ( 2 FDA reports)
DIABETES MELLITUS ( 2 FDA reports)
EX-SMOKER ( 2 FDA reports)
FATIGUE ( 2 FDA reports)
HYPERHIDROSIS ( 2 FDA reports)
MULTIPLE SCLEROSIS ( 2 FDA reports)
MUSCULOSKELETAL CHEST PAIN ( 2 FDA reports)
NAUSEA ( 2 FDA reports)
OPTIC NEURITIS ( 2 FDA reports)
OXYGEN SATURATION DECREASED ( 2 FDA reports)
PAIN IN EXTREMITY ( 2 FDA reports)
PSYCHOMOTOR HYPERACTIVITY ( 2 FDA reports)
REFUSAL OF TREATMENT BY PATIENT ( 2 FDA reports)
SLEEP APNOEA SYNDROME ( 2 FDA reports)
SPEECH DISORDER ( 2 FDA reports)
STRESS FRACTURE ( 2 FDA reports)
URINARY TRACT INFECTION ( 2 FDA reports)
ABNORMAL BEHAVIOUR ( 1 FDA reports)
ANAPHYLACTIC REACTION ( 1 FDA reports)
ANKLE FRACTURE ( 1 FDA reports)
APHASIA ( 1 FDA reports)
ARTERIAL OCCLUSIVE DISEASE ( 1 FDA reports)
ARTHRALGIA ( 1 FDA reports)
BASAL CELL CARCINOMA ( 1 FDA reports)
BLINDNESS ( 1 FDA reports)
BLOOD PRESSURE ABNORMAL ( 1 FDA reports)
BLOOD PRESSURE INCREASED ( 1 FDA reports)
BLOOD PROLACTIN INCREASED ( 1 FDA reports)
BRONCHITIS ( 1 FDA reports)
CHILLS ( 1 FDA reports)
CHRONIC OBSTRUCTIVE PULMONARY DISEASE ( 1 FDA reports)
CONSTIPATION ( 1 FDA reports)
CYSTITIS ( 1 FDA reports)
CYSTITIS ESCHERICHIA ( 1 FDA reports)
DEHYDRATION ( 1 FDA reports)
DELUSION ( 1 FDA reports)
DIARRHOEA HAEMORRHAGIC ( 1 FDA reports)
DISEASE COMPLICATION ( 1 FDA reports)
DISORIENTATION ( 1 FDA reports)
DRUG INTOLERANCE ( 1 FDA reports)
DYSPEPSIA ( 1 FDA reports)
DYSSTASIA ( 1 FDA reports)
ECONOMIC PROBLEM ( 1 FDA reports)
EXTRASYSTOLES ( 1 FDA reports)
EYE PAIN ( 1 FDA reports)
FAECAL INCONTINENCE ( 1 FDA reports)
FLUID RETENTION ( 1 FDA reports)
FRACTURE DELAYED UNION ( 1 FDA reports)
FUNGAL INFECTION ( 1 FDA reports)
HALLUCINATION ( 1 FDA reports)
HEAD INJURY ( 1 FDA reports)
HEART RATE DECREASED ( 1 FDA reports)
HEART RATE INCREASED ( 1 FDA reports)
HEPATITIS ( 1 FDA reports)
HYPERSENSITIVITY ( 1 FDA reports)
HYPOAESTHESIA FACIAL ( 1 FDA reports)
IMMOBILE ( 1 FDA reports)
IMPAIRED HEALING ( 1 FDA reports)
INFLUENZA LIKE ILLNESS ( 1 FDA reports)
INJECTION SITE NECROSIS ( 1 FDA reports)
LOSS OF CONSCIOUSNESS ( 1 FDA reports)
LUMBAR PUNCTURE ABNORMAL ( 1 FDA reports)
LUNG NEOPLASM ( 1 FDA reports)
MENINGITIS VIRAL ( 1 FDA reports)
MICTURITION URGENCY ( 1 FDA reports)
MIGRAINE ( 1 FDA reports)
MOBILITY DECREASED ( 1 FDA reports)
MULTIPLE SCLEROSIS RELAPSE ( 1 FDA reports)
MUSCLE SPASTICITY ( 1 FDA reports)
MUSCULAR WEAKNESS ( 1 FDA reports)
MYALGIA ( 1 FDA reports)
MYOCARDIAL INFARCTION ( 1 FDA reports)
NASOPHARYNGITIS ( 1 FDA reports)
NO THERAPEUTIC RESPONSE ( 1 FDA reports)
OEDEMA PERIPHERAL ( 1 FDA reports)
PARANOIA ( 1 FDA reports)
PSYCHOTIC DISORDER ( 1 FDA reports)
PULMONARY EMBOLISM ( 1 FDA reports)
PULMONARY OEDEMA ( 1 FDA reports)
PYREXIA ( 1 FDA reports)
RED BLOOD CELL COUNT DECREASED ( 1 FDA reports)
RHEUMATOID ARTHRITIS ( 1 FDA reports)
RIB FRACTURE ( 1 FDA reports)
ROAD TRAFFIC ACCIDENT ( 1 FDA reports)
SHOCK ( 1 FDA reports)
SICK RELATIVE ( 1 FDA reports)
STRESS ( 1 FDA reports)
SWELLING ( 1 FDA reports)
SWELLING FACE ( 1 FDA reports)
SYSTEMIC LUPUS ERYTHEMATOSUS ( 1 FDA reports)
THROMBOSIS ( 1 FDA reports)
URINARY INCONTINENCE ( 1 FDA reports)
URINARY RETENTION ( 1 FDA reports)
VITREOUS FLOATERS ( 1 FDA reports)
VOMITING ( 1 FDA reports)
WHIPLASH INJURY ( 1 FDA reports)
WHITE BLOOD CELL COUNT DECREASED ( 1 FDA reports)

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