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

MYOCLONUS ( 23 FDA reports)
DYSTONIA ( 18 FDA reports)
MOVEMENT DISORDER ( 18 FDA reports)
DRUG INTERACTION ( 17 FDA reports)
MYOTONIA ( 17 FDA reports)
SINUS TACHYCARDIA ( 16 FDA reports)
DIARRHOEA ( 9 FDA reports)
ACQUIRED CLAW TOE ( 7 FDA reports)
ACUTE MYOCARDIAL INFARCTION ( 7 FDA reports)
ANGINA UNSTABLE ( 7 FDA reports)
ARTHROPATHY ( 7 FDA reports)
BACK PAIN ( 7 FDA reports)
BLOOD PRESSURE INCREASED ( 7 FDA reports)
BURSITIS ( 7 FDA reports)
CAROTID ARTERY STENOSIS ( 7 FDA reports)
CEREBROVASCULAR ACCIDENT ( 7 FDA reports)
DIABETES MELLITUS NON-INSULIN-DEPENDENT ( 7 FDA reports)
HEADACHE ( 7 FDA reports)
MYOCARDIAL INFARCTION ( 7 FDA reports)
TENDONITIS ( 7 FDA reports)
HAEMARTHROSIS ( 6 FDA reports)
MONARTHRITIS ( 6 FDA reports)
ANGIOEDEMA ( 5 FDA reports)
INJURY ( 5 FDA reports)
SLEEP APNOEA SYNDROME ( 5 FDA reports)
ANAPHYLACTIC SHOCK ( 4 FDA reports)
ASTHENIA ( 4 FDA reports)
CARDIAC ARREST ( 4 FDA reports)
CARPAL TUNNEL SYNDROME ( 4 FDA reports)
COLITIS ( 4 FDA reports)
CONVULSION ( 4 FDA reports)
DIABETIC NEUROPATHY ( 4 FDA reports)
DIABETIC RETINOPATHY ( 4 FDA reports)
ENDOTRACHEAL INTUBATION ( 4 FDA reports)
GRAND MAL CONVULSION ( 4 FDA reports)
OBSTRUCTIVE AIRWAYS DISORDER ( 4 FDA reports)
PERITONITIS ( 4 FDA reports)
PNEUMATOSIS INTESTINALIS ( 4 FDA reports)
PNEUMONIA ( 4 FDA reports)
POST-ANOXIC MYOCLONUS ( 4 FDA reports)
RESPIRATORY DISTRESS ( 4 FDA reports)
SEPSIS ( 4 FDA reports)
ACUTE RESPIRATORY DISTRESS SYNDROME ( 3 FDA reports)
BASAL CELL CARCINOMA ( 3 FDA reports)
DERMATITIS CONTACT ( 3 FDA reports)
ELECTROMECHANICAL DISSOCIATION ( 3 FDA reports)
EPISTAXIS ( 3 FDA reports)
MEDICATION ERROR ( 3 FDA reports)
MOUTH HAEMORRHAGE ( 3 FDA reports)
MULTI-ORGAN FAILURE ( 3 FDA reports)
SKIN TEST POSITIVE ( 3 FDA reports)
CORONARY ARTERY DISEASE ( 2 FDA reports)
CORONARY ARTERY RESTENOSIS ( 2 FDA reports)
DELIRIUM ( 2 FDA reports)
HEARING IMPAIRED ( 2 FDA reports)
INTERMITTENT CLAUDICATION ( 2 FDA reports)
MYOCARDIAL ISCHAEMIA ( 2 FDA reports)
VERTIGO ( 2 FDA reports)
VESTIBULAR DISORDER ( 2 FDA reports)
ABORTION INDUCED ( 1 FDA reports)
ACTIVATED PARTIAL THROMBOPLASTIN TIME SHORTENED ( 1 FDA reports)
AGITATION ( 1 FDA reports)
AKATHISIA ( 1 FDA reports)
ANAPHYLACTIC REACTION ( 1 FDA reports)
ARTERIAL INSUFFICIENCY ( 1 FDA reports)
BLOOD CALCIUM INCREASED ( 1 FDA reports)
BLOOD PHOSPHORUS INCREASED ( 1 FDA reports)
BRONCHOSPASM ( 1 FDA reports)
C-REACTIVE PROTEIN INCREASED ( 1 FDA reports)
CALCINOSIS ( 1 FDA reports)
CORONARY ARTERY DISSECTION ( 1 FDA reports)
CORONARY ARTERY OCCLUSION ( 1 FDA reports)
CORONARY ARTERY STENOSIS ( 1 FDA reports)
CORONARY OSTIAL STENOSIS ( 1 FDA reports)
DRUG EXPOSURE DURING PREGNANCY ( 1 FDA reports)
DRUG INEFFECTIVE ( 1 FDA reports)
DRUG TOXICITY ( 1 FDA reports)
DYSPNOEA ( 1 FDA reports)
ENDOTRACHEAL INTUBATION COMPLICATION ( 1 FDA reports)
EXTENSOR PLANTAR RESPONSE ( 1 FDA reports)
FALL ( 1 FDA reports)
FEELING ABNORMAL ( 1 FDA reports)
GLASGOW COMA SCALE ABNORMAL ( 1 FDA reports)
GLOSSODYNIA ( 1 FDA reports)
HAEMATOMA ( 1 FDA reports)
HAEMORRHAGE ( 1 FDA reports)
HYPERREFLEXIA ( 1 FDA reports)
HYPOCAPNIA ( 1 FDA reports)
INTRACARDIAC THROMBUS ( 1 FDA reports)
JOINT DISLOCATION ( 1 FDA reports)
LUMBAR RADICULOPATHY ( 1 FDA reports)
MYDRIASIS ( 1 FDA reports)
NEUROPATHY ( 1 FDA reports)
NEUROPATHY PERIPHERAL ( 1 FDA reports)
NO THERAPEUTIC RESPONSE ( 1 FDA reports)
OSTEOARTHRITIS ( 1 FDA reports)
OXYGEN SATURATION DECREASED ( 1 FDA reports)
PLATELET COUNT DECREASED ( 1 FDA reports)
PROTHROMBIN LEVEL DECREASED ( 1 FDA reports)
PULSE ABSENT ( 1 FDA reports)
PUPILLARY REFLEX IMPAIRED ( 1 FDA reports)
RESPIRATORY FAILURE ( 1 FDA reports)
RESTLESSNESS ( 1 FDA reports)
RETAINED PRODUCTS OF CONCEPTION ( 1 FDA reports)
ROTATOR CUFF SYNDROME ( 1 FDA reports)
SEROTONIN SYNDROME ( 1 FDA reports)
SEX CHROMOSOME ABNORMALITY ( 1 FDA reports)
SPEECH DISORDER ( 1 FDA reports)
STARING ( 1 FDA reports)
SUPRAVENTRICULAR TACHYCARDIA ( 1 FDA reports)
SWOLLEN TONGUE ( 1 FDA reports)
TREATMENT NONCOMPLIANCE ( 1 FDA reports)
URTICARIA ( 1 FDA reports)
VENTRICULAR FIBRILLATION ( 1 FDA reports)
WHITE BLOOD CELL COUNT DECREASED ( 1 FDA reports)
WHITE BLOOD CELL COUNT INCREASED ( 1 FDA reports)
Y-LINKED CHROMOSOMAL DISORDER ( 1 FDA reports)

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