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

DEPRESSION ( 3 FDA reports)
ANXIETY ( 2 FDA reports)
ARRHYTHMIA ( 2 FDA reports)
DIFFICULTY IN WALKING ( 2 FDA reports)
DIZZINESS ( 2 FDA reports)
FALL ( 2 FDA reports)
HYPERTENSION ( 2 FDA reports)
HYPOKALAEMIA ( 2 FDA reports)
INSOMNIA ( 2 FDA reports)
MALAISE ( 2 FDA reports)
MEMORY IMPAIRMENT ( 2 FDA reports)
NERVE INJURY ( 2 FDA reports)
OPTIC ISCHAEMIC NEUROPATHY ( 2 FDA reports)
PAIN ( 2 FDA reports)
PAIN IN EXTREMITY ( 2 FDA reports)
ABDOMINAL PAIN UPPER ( 1 FDA reports)
ABNORMAL BEHAVIOUR ( 1 FDA reports)
AGGRESSION ( 1 FDA reports)
ARRHYTHMIA SUPRAVENTRICULAR ( 1 FDA reports)
ARTERIAL OCCLUSIVE DISEASE ( 1 FDA reports)
ARTHRALGIA ( 1 FDA reports)
ASTHENIA ( 1 FDA reports)
ATRIAL FIBRILLATION ( 1 FDA reports)
ATRIAL FLUTTER ( 1 FDA reports)
ATRIOVENTRICULAR BLOCK FIRST DEGREE ( 1 FDA reports)
ATRIOVENTRICULAR BLOCK SECOND DEGREE ( 1 FDA reports)
BLOOD GLUCOSE INCREASED ( 1 FDA reports)
BLOOD MAGNESIUM DECREASED ( 1 FDA reports)
BODY HEIGHT DECREASED ( 1 FDA reports)
BRADYCARDIA ( 1 FDA reports)
BREAST CANCER ( 1 FDA reports)
BREAST HAEMORRHAGE ( 1 FDA reports)
BUNDLE BRANCH BLOCK RIGHT ( 1 FDA reports)
BURNING SENSATION ( 1 FDA reports)
CARDIAC DISORDER ( 1 FDA reports)
CARDIAC FAILURE ( 1 FDA reports)
CARDIAC FAILURE CONGESTIVE ( 1 FDA reports)
CERVICAL VERTEBRAL FRACTURE ( 1 FDA reports)
CHEST DISCOMFORT ( 1 FDA reports)
CHEST PAIN ( 1 FDA reports)
CONDITION AGGRAVATED ( 1 FDA reports)
CONDUCTION DISORDER ( 1 FDA reports)
CONSTIPATION ( 1 FDA reports)
CONTUSION ( 1 FDA reports)
COUGH ( 1 FDA reports)
CREATINE PHOSPHOKINASE DECREASED ( 1 FDA reports)
CYCLOTHYMIC DISORDER ( 1 FDA reports)
DECREASED ACTIVITY ( 1 FDA reports)
DIARRHOEA ( 1 FDA reports)
DILATATION ATRIAL ( 1 FDA reports)
DRUG EFFECT DECREASED ( 1 FDA reports)
DRUG INEFFECTIVE ( 1 FDA reports)
DRY MOUTH ( 1 FDA reports)
DYSPEPSIA ( 1 FDA reports)
ECCHYMOSIS ( 1 FDA reports)
ELECTROCARDIOGRAM ST SEGMENT DEPRESSION ( 1 FDA reports)
ELECTROCARDIOGRAM ST-T SEGMENT ABNORMAL ( 1 FDA reports)
ELECTROCARDIOGRAM T WAVE INVERSION ( 1 FDA reports)
EXTRASYSTOLES ( 1 FDA reports)
FACE INJURY ( 1 FDA reports)
FATIGUE ( 1 FDA reports)
FEELING ABNORMAL ( 1 FDA reports)
FEELING HOT ( 1 FDA reports)
FLUSHING ( 1 FDA reports)
GRANULOCYTOPENIA ( 1 FDA reports)
HAEMATOMA ( 1 FDA reports)
HEAD INJURY ( 1 FDA reports)
HEADACHE ( 1 FDA reports)
HEAT EXHAUSTION ( 1 FDA reports)
HYPOCALCAEMIA ( 1 FDA reports)
HYPOMANIA ( 1 FDA reports)
HYPOTENSION ( 1 FDA reports)
IMPLANT SITE REACTION ( 1 FDA reports)
INDIFFERENCE ( 1 FDA reports)
INJURY ( 1 FDA reports)
LIMB INJURY ( 1 FDA reports)
LIP DRY ( 1 FDA reports)
MENTAL DISORDER ( 1 FDA reports)
MOBILITY DECREASED ( 1 FDA reports)
MUSCLE CRAMP ( 1 FDA reports)
MUSCLE DISORDER ( 1 FDA reports)
MUSCLE INJURY ( 1 FDA reports)
MYOCARDIAL ISCHAEMIA ( 1 FDA reports)
NAUSEA ( 1 FDA reports)
NECK PAIN ( 1 FDA reports)
NERVOUS SYSTEM DISORDER ( 1 FDA reports)
NERVOUSNESS ( 1 FDA reports)
NODAL RHYTHM ( 1 FDA reports)
OEDEMA PERIPHERAL ( 1 FDA reports)
OSTEOPENIA ( 1 FDA reports)
OSTEOPOROSIS ( 1 FDA reports)
PALPITATIONS ( 1 FDA reports)
PANCREATITIS ( 1 FDA reports)
PANIC ATTACK ( 1 FDA reports)
PHARMACEUTICAL PRODUCT COMPLAINT ( 1 FDA reports)
PLEURAL FIBROSIS ( 1 FDA reports)
RASH PRURITIC ( 1 FDA reports)
REFUSAL OF TREATMENT BY PATIENT ( 1 FDA reports)
RESPIRATORY ARREST ( 1 FDA reports)
RHEUMATOID ARTHRITIS ( 1 FDA reports)
RIB FRACTURE ( 1 FDA reports)
SEDATION ( 1 FDA reports)
SEXUAL DYSFUNCTION ( 1 FDA reports)
SHOULDER PAIN ( 1 FDA reports)
SINUS ARRHYTHMIA ( 1 FDA reports)
SINUS BRADYCARDIA ( 1 FDA reports)
SPINAL FRACTURE ( 1 FDA reports)
STOMACH DISCOMFORT ( 1 FDA reports)
SUPRAVENTRICULAR EXTRASYSTOLES ( 1 FDA reports)
SWELLING ( 1 FDA reports)
SYNCOPE ( 1 FDA reports)
TETANY ( 1 FDA reports)
TREATMENT NONCOMPLIANCE ( 1 FDA reports)
URINARY TRACT OPERATION ( 1 FDA reports)
VENTRICULAR EXTRASYSTOLES ( 1 FDA reports)
VENTRICULAR TACHYCARDIA ( 1 FDA reports)
WEIGHT DECREASED ( 1 FDA reports)
WEIGHT INCREASED ( 1 FDA reports)

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