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

APHASIA ( 14 FDA reports)
DIARRHOEA ( 14 FDA reports)
PARAESTHESIA ( 13 FDA reports)
CONFUSIONAL STATE ( 11 FDA reports)
HEADACHE ( 11 FDA reports)
HYPERTONIA ( 11 FDA reports)
MEMORY IMPAIRMENT ( 11 FDA reports)
ANXIETY ( 10 FDA reports)
FEELING ABNORMAL ( 10 FDA reports)
INSOMNIA ( 10 FDA reports)
MANIA ( 10 FDA reports)
TREMOR ( 10 FDA reports)
BALANCE DISORDER ( 9 FDA reports)
ACCOMMODATION DISORDER ( 8 FDA reports)
AGITATION ( 8 FDA reports)
AKATHISIA ( 8 FDA reports)
ANGER ( 8 FDA reports)
ARRHYTHMIA ( 8 FDA reports)
BLOOD PRESSURE INCREASED ( 8 FDA reports)
CONDITION AGGRAVATED ( 8 FDA reports)
CONDUCTION DISORDER ( 8 FDA reports)
CRYING ( 8 FDA reports)
DISABILITY ( 8 FDA reports)
DISTURBANCE IN SOCIAL BEHAVIOUR ( 8 FDA reports)
DRUG EFFECT DECREASED ( 8 FDA reports)
DRUG WITHDRAWAL SYNDROME ( 8 FDA reports)
DYSARTHRIA ( 8 FDA reports)
DYSTONIA ( 8 FDA reports)
ECONOMIC PROBLEM ( 8 FDA reports)
EMOTIONAL DISTRESS ( 8 FDA reports)
FOOT DEFORMITY ( 8 FDA reports)
HAEMORRHAGE ( 8 FDA reports)
HAND DEFORMITY ( 8 FDA reports)
HEAD TITUBATION ( 8 FDA reports)
HEART RATE INCREASED ( 8 FDA reports)
HOMELESS ( 8 FDA reports)
HYPOMANIA ( 8 FDA reports)
IRRITABILITY ( 8 FDA reports)
LARYNGOSPASM ( 8 FDA reports)
LOSS OF EMPLOYMENT ( 8 FDA reports)
MENTAL DISORDER ( 8 FDA reports)
MOBILITY DECREASED ( 8 FDA reports)
PAIN ( 8 FDA reports)
PANIC ATTACK ( 8 FDA reports)
PARKINSONISM ( 8 FDA reports)
PLANTAR FASCIITIS ( 8 FDA reports)
RESTLESS LEGS SYNDROME ( 8 FDA reports)
SEDATION ( 8 FDA reports)
SELF ESTEEM DECREASED ( 8 FDA reports)
SEROTONIN SYNDROME ( 8 FDA reports)
SLEEP DISORDER ( 8 FDA reports)
SUICIDAL IDEATION ( 8 FDA reports)
TONGUE PARALYSIS ( 8 FDA reports)
DYSPNOEA ( 7 FDA reports)
NAUSEA ( 7 FDA reports)
PYREXIA ( 7 FDA reports)
CHILLS ( 6 FDA reports)
ENCEPHALOPATHY ( 6 FDA reports)
NEUROMYOPATHY ( 6 FDA reports)
ASTHENIA ( 5 FDA reports)
DEPRESSION ( 5 FDA reports)
DISORIENTATION ( 5 FDA reports)
DISTURBANCE IN ATTENTION ( 5 FDA reports)
HYPOAESTHESIA ( 5 FDA reports)
RESTLESSNESS ( 5 FDA reports)
DECREASED APPETITE ( 4 FDA reports)
DISSOCIATIVE DISORDER ( 4 FDA reports)
HAEMOGLOBIN DECREASED ( 4 FDA reports)
ACTIVITIES OF DAILY LIVING IMPAIRED ( 3 FDA reports)
AFFECT LABILITY ( 3 FDA reports)
BLOOD PRESSURE SYSTOLIC INCREASED ( 3 FDA reports)
DIZZINESS ( 3 FDA reports)
FEELING GUILTY ( 3 FDA reports)
ILLUSION ( 3 FDA reports)
MENTAL STATUS CHANGES ( 3 FDA reports)
MULTIPLE SCLEROSIS RELAPSE ( 3 FDA reports)
OBESITY ( 3 FDA reports)
PROTEIN TOTAL INCREASED ( 3 FDA reports)
SOMATOFORM DISORDER ( 3 FDA reports)
SPINAL OSTEOARTHRITIS ( 3 FDA reports)
SUSPICIOUSNESS ( 3 FDA reports)
TOOTH ABSCESS ( 3 FDA reports)
ABASIA ( 2 FDA reports)
ANOREXIA ( 2 FDA reports)
BLEPHAROSPASM ( 2 FDA reports)
BLINDNESS TRANSIENT ( 2 FDA reports)
BURNING SENSATION ( 2 FDA reports)
COUGH ( 2 FDA reports)
DRY EYE ( 2 FDA reports)
FATIGUE ( 2 FDA reports)
IMPAIRED DRIVING ABILITY ( 2 FDA reports)
METAMORPHOPSIA ( 2 FDA reports)
MUSCLE SPASMS ( 2 FDA reports)
MUSCLE TWITCHING ( 2 FDA reports)
SPINAL DEFORMITY ( 2 FDA reports)
TENDON PAIN ( 2 FDA reports)
TENDONITIS ( 2 FDA reports)
WHITE BLOOD CELL COUNT INCREASED ( 2 FDA reports)
ABDOMINAL DISTENSION ( 1 FDA reports)
ABDOMINAL PAIN ( 1 FDA reports)
ABSCESS ( 1 FDA reports)
ACQUIRED OESOPHAGEAL WEB ( 1 FDA reports)
AGGRESSION ( 1 FDA reports)
AMNESIA ( 1 FDA reports)
ANGIOPLASTY ( 1 FDA reports)
APPENDICITIS ( 1 FDA reports)
ATAXIA ( 1 FDA reports)
BACK PAIN ( 1 FDA reports)
BASEDOW'S DISEASE ( 1 FDA reports)
BLOOD ALBUMIN DECREASED ( 1 FDA reports)
BLOOD BILIRUBIN INCREASED ( 1 FDA reports)
BLOOD CALCIUM DECREASED ( 1 FDA reports)
BLOOD CREATININE INCREASED ( 1 FDA reports)
BLOOD POTASSIUM DECREASED ( 1 FDA reports)
C-REACTIVE PROTEIN INCREASED ( 1 FDA reports)
CARBOHYDRATE ANTIGEN 125 INCREASED ( 1 FDA reports)
CARDIAC FAILURE CONGESTIVE ( 1 FDA reports)
CARDIAC MURMUR ( 1 FDA reports)
CARDIOACTIVE DRUG LEVEL DECREASED ( 1 FDA reports)
CARDIOMEGALY ( 1 FDA reports)
CARDIOMYOPATHY ( 1 FDA reports)
CAROTID ARTERY STENOSIS ( 1 FDA reports)
CAROTID BRUIT ( 1 FDA reports)
CATHETERISATION CARDIAC ABNORMAL ( 1 FDA reports)
CEREBELLAR SYNDROME ( 1 FDA reports)
CEREBROVASCULAR ACCIDENT ( 1 FDA reports)
CHEST DISCOMFORT ( 1 FDA reports)
CHEST PAIN ( 1 FDA reports)
CHEST X-RAY ABNORMAL ( 1 FDA reports)
COLON CANCER ( 1 FDA reports)
COLON CANCER METASTATIC ( 1 FDA reports)
COMPUTERISED TOMOGRAM ABNORMAL ( 1 FDA reports)
CORONARY ARTERIAL STENT INSERTION ( 1 FDA reports)
CORONARY ARTERY DISEASE ( 1 FDA reports)
CSF PROTEIN INCREASED ( 1 FDA reports)
DEHYDRATION ( 1 FDA reports)
DELUSION ( 1 FDA reports)
DIABETES MELLITUS ( 1 FDA reports)
DRY MOUTH ( 1 FDA reports)
DYSURIA ( 1 FDA reports)
ECHOCARDIOGRAM ABNORMAL ( 1 FDA reports)
EJECTION FRACTION DECREASED ( 1 FDA reports)
ELECTROCARDIOGRAM ABNORMAL ( 1 FDA reports)
EYE PAIN ( 1 FDA reports)
FACIAL PARESIS ( 1 FDA reports)
FOLLICULITIS ( 1 FDA reports)
GAIT DISTURBANCE ( 1 FDA reports)
GASTROINTESTINAL CANDIDIASIS ( 1 FDA reports)
GASTROOESOPHAGEAL REFLUX DISEASE ( 1 FDA reports)
HAEMATEMESIS ( 1 FDA reports)
HALLUCINATION ( 1 FDA reports)
HEMIPARESIS ( 1 FDA reports)
HEPATIC ENZYME ABNORMAL ( 1 FDA reports)
HEPATIC ENZYME INCREASED ( 1 FDA reports)
HOT FLUSH ( 1 FDA reports)
HYPERAESTHESIA ( 1 FDA reports)
HYPERCHOLESTEROLAEMIA ( 1 FDA reports)
HYPERTENSION ( 1 FDA reports)
HYPOTENSION ( 1 FDA reports)
ILL-DEFINED DISORDER ( 1 FDA reports)
INFERIOR VENA CAVA SYNDROME ( 1 FDA reports)
INTENTIONAL DRUG MISUSE ( 1 FDA reports)
LACUNAR INFARCTION ( 1 FDA reports)
LEFT VENTRICULAR HYPERTROPHY ( 1 FDA reports)
LEUKOPENIA ( 1 FDA reports)
LOSS OF CONSCIOUSNESS ( 1 FDA reports)
LUNG NEOPLASM ( 1 FDA reports)
MEAN CELL VOLUME INCREASED ( 1 FDA reports)
METASTASES TO LYMPH NODES ( 1 FDA reports)
MITRAL VALVE DISEASE MIXED ( 1 FDA reports)
MITRAL VALVE INCOMPETENCE ( 1 FDA reports)
MUSCULAR WEAKNESS ( 1 FDA reports)
NASAL CANDIDIASIS ( 1 FDA reports)
NASOPHARYNGITIS ( 1 FDA reports)
NIGHT SWEATS ( 1 FDA reports)
NUCLEAR MAGNETIC RESONANCE IMAGING BRAIN ABNORMAL ( 1 FDA reports)
OESOPHAGEAL DISORDER ( 1 FDA reports)
OESOPHAGEAL OPERATION ( 1 FDA reports)
OESOPHAGEAL ULCER ( 1 FDA reports)
ORAL CANDIDIASIS ( 1 FDA reports)
OVERDOSE ( 1 FDA reports)
PAIN OF SKIN ( 1 FDA reports)
PALPITATIONS ( 1 FDA reports)
PARAPARESIS ( 1 FDA reports)
PELVIC PAIN ( 1 FDA reports)
PERIPHERAL VASCULAR DISORDER ( 1 FDA reports)
PHARMACEUTICAL PRODUCT COMPLAINT ( 1 FDA reports)
PLEURAL NEOPLASM ( 1 FDA reports)
PNEUMONIA ( 1 FDA reports)
PRESYNCOPE ( 1 FDA reports)
PULMONARY HYPERTENSION ( 1 FDA reports)
RASH PRURITIC ( 1 FDA reports)
RED BLOOD CELL SEDIMENTATION RATE ABNORMAL ( 1 FDA reports)
RENAL IMPAIRMENT ( 1 FDA reports)
RESPIRATORY FAILURE ( 1 FDA reports)
RETCHING ( 1 FDA reports)
SCAN MYOCARDIAL PERFUSION ABNORMAL ( 1 FDA reports)
SINUS BRADYCARDIA ( 1 FDA reports)
SKIN HYPERPIGMENTATION ( 1 FDA reports)
SPEECH DISORDER ( 1 FDA reports)
SPINAL NERVE STIMULATOR IMPLANTATION ( 1 FDA reports)
SUPRAVENTRICULAR EXTRASYSTOLES ( 1 FDA reports)
THROMBOSIS ( 1 FDA reports)
TIC ( 1 FDA reports)
TOXIC ENCEPHALOPATHY ( 1 FDA reports)
TOXICITY TO VARIOUS AGENTS ( 1 FDA reports)
VENTRICULAR EXTRASYSTOLES ( 1 FDA reports)
VISUAL DISTURBANCE ( 1 FDA reports)
VOMITING ( 1 FDA reports)
WHITE BLOOD CELL COUNT DECREASED ( 1 FDA reports)

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