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

SUICIDAL IDEATION ( 17 FDA reports)
DEPRESSION ( 15 FDA reports)
ADVERSE EVENT ( 12 FDA reports)
MOOD SWINGS ( 12 FDA reports)
AGGRESSION ( 10 FDA reports)
ABNORMAL BEHAVIOUR ( 8 FDA reports)
AGITATION ( 8 FDA reports)
AMNESIA ( 8 FDA reports)
ANTISOCIAL BEHAVIOUR ( 8 FDA reports)
APATHY ( 8 FDA reports)
BIPOLAR DISORDER ( 8 FDA reports)
CRYING ( 8 FDA reports)
DECREASED APPETITE ( 8 FDA reports)
DECREASED INTEREST ( 8 FDA reports)
DISTURBANCE IN ATTENTION ( 8 FDA reports)
DISTURBANCE IN SOCIAL BEHAVIOUR ( 8 FDA reports)
DRUG ABUSE ( 8 FDA reports)
INSOMNIA ( 8 FDA reports)
INTENTIONAL SELF-INJURY ( 8 FDA reports)
IRRITABILITY ( 8 FDA reports)
PSYCHOTIC DISORDER ( 8 FDA reports)
SEXUAL ABUSE ( 8 FDA reports)
SHOPLIFTING ( 8 FDA reports)
SOCIAL AVOIDANT BEHAVIOUR ( 8 FDA reports)
SUBSTANCE ABUSE ( 8 FDA reports)
SUICIDE ATTEMPT ( 8 FDA reports)
FALL ( 7 FDA reports)
SINUSITIS ( 7 FDA reports)
DYSPNOEA ( 6 FDA reports)
FEMUR FRACTURE ( 6 FDA reports)
HYPERTENSION ( 6 FDA reports)
ARTHRALGIA ( 5 FDA reports)
CHEST PAIN ( 5 FDA reports)
FATIGUE ( 5 FDA reports)
GASTROOESOPHAGEAL REFLUX DISEASE ( 5 FDA reports)
HEADACHE ( 5 FDA reports)
HYPERLIPIDAEMIA ( 5 FDA reports)
MYOCARDIAL INFARCTION ( 5 FDA reports)
RHABDOMYOLYSIS ( 5 FDA reports)
CARPAL TUNNEL SYNDROME ( 4 FDA reports)
CEREBROVASCULAR ACCIDENT ( 4 FDA reports)
CORONARY ARTERY DISEASE ( 4 FDA reports)
DERMATITIS CONTACT ( 4 FDA reports)
FIBROCYSTIC BREAST DISEASE ( 4 FDA reports)
INTERVERTEBRAL DISC DEGENERATION ( 4 FDA reports)
SPONDYLOLISTHESIS ( 4 FDA reports)
SUBDURAL HAEMORRHAGE ( 4 FDA reports)
ACUTE MYOCARDIAL INFARCTION ( 3 FDA reports)
ANXIETY ( 3 FDA reports)
ARTERIOSCLEROSIS CORONARY ARTERY ( 3 FDA reports)
CARDIAC FLUTTER ( 3 FDA reports)
CHEST DISCOMFORT ( 3 FDA reports)
COMPLETED SUICIDE ( 3 FDA reports)
CONJUNCTIVITIS ALLERGIC ( 3 FDA reports)
CONVULSION ( 3 FDA reports)
CORONARY ARTERY OCCLUSION ( 3 FDA reports)
CYST ( 3 FDA reports)
DEPRESSED MOOD ( 3 FDA reports)
DERMAL CYST ( 3 FDA reports)
DIZZINESS ( 3 FDA reports)
DYSPEPSIA ( 3 FDA reports)
ECZEMA ( 3 FDA reports)
HAEMATOCRIT DECREASED ( 3 FDA reports)
JOINT INJURY ( 3 FDA reports)
JOINT SPRAIN ( 3 FDA reports)
OSTEOARTHRITIS ( 3 FDA reports)
POLYCYTHAEMIA ( 3 FDA reports)
SKIN LESION ( 3 FDA reports)
STRESS ( 3 FDA reports)
THROAT IRRITATION ( 3 FDA reports)
TRANSIENT ISCHAEMIC ATTACK ( 3 FDA reports)
URTICARIA CHRONIC ( 3 FDA reports)
VISION BLURRED ( 3 FDA reports)
VULVOVAGINAL DRYNESS ( 3 FDA reports)
ALLERGIC GRANULOMATOUS ANGIITIS ( 2 FDA reports)
AORTIC ARTERIOSCLEROSIS ( 2 FDA reports)
ATRIAL SEPTAL DEFECT ( 2 FDA reports)
BACK PAIN ( 2 FDA reports)
BLOOD CHOLESTEROL INCREASED ( 2 FDA reports)
BREAST ENLARGEMENT ( 2 FDA reports)
BREAST PAIN ( 2 FDA reports)
BURSITIS ( 2 FDA reports)
CARDIAC MURMUR ( 2 FDA reports)
CIRCULATORY COLLAPSE ( 2 FDA reports)
DEAFNESS ( 2 FDA reports)
DEHYDRATION ( 2 FDA reports)
DENTAL CARIES ( 2 FDA reports)
DIARRHOEA ( 2 FDA reports)
DROOLING ( 2 FDA reports)
DRUG HYPERSENSITIVITY ( 2 FDA reports)
DRUG INEFFECTIVE ( 2 FDA reports)
DYSARTHRIA ( 2 FDA reports)
DYSPHONIA ( 2 FDA reports)
ELECTROCARDIOGRAM ABNORMAL ( 2 FDA reports)
ENDOCARDITIS ( 2 FDA reports)
EXERCISE TEST ABNORMAL ( 2 FDA reports)
EYE IRRITATION ( 2 FDA reports)
FEMORAL NECK FRACTURE ( 2 FDA reports)
FOOT DEFORMITY ( 2 FDA reports)
GASTROINTESTINAL DISORDER ( 2 FDA reports)
GLUCOSE TOLERANCE IMPAIRED ( 2 FDA reports)
HUMAN PAPILLOMA VIRUS TEST POSITIVE ( 2 FDA reports)
HYPERCHOLESTEROLAEMIA ( 2 FDA reports)
HYPERTRIGLYCERIDAEMIA ( 2 FDA reports)
INJURY ( 2 FDA reports)
INTERVERTEBRAL DISC DISORDER ( 2 FDA reports)
INTERVERTEBRAL DISC PROTRUSION ( 2 FDA reports)
JOINT EFFUSION ( 2 FDA reports)
LONG THORACIC NERVE PALSY ( 2 FDA reports)
LOW TURNOVER OSTEOPATHY ( 2 FDA reports)
LUMBAR RADICULOPATHY ( 2 FDA reports)
MENTAL DISORDER ( 2 FDA reports)
MITRAL VALVE INCOMPETENCE ( 2 FDA reports)
MUSCLE SPASMS ( 2 FDA reports)
MUSCLE STRAIN ( 2 FDA reports)
NASOPHARYNGITIS ( 2 FDA reports)
NEPHROLITHIASIS ( 2 FDA reports)
NEUROPATHY PERIPHERAL ( 2 FDA reports)
NOCTURIA ( 2 FDA reports)
OEDEMA PERIPHERAL ( 2 FDA reports)
OVARIAN CYST ( 2 FDA reports)
PAIN IN EXTREMITY ( 2 FDA reports)
PALPITATIONS ( 2 FDA reports)
PLANTAR FASCIITIS ( 2 FDA reports)
POST PROCEDURAL COMPLICATION ( 2 FDA reports)
PRURITUS ( 2 FDA reports)
PULMONARY VALVE INCOMPETENCE ( 2 FDA reports)
RENAL CYST ( 2 FDA reports)
RESTLESS LEGS SYNDROME ( 2 FDA reports)
SCIATICA ( 2 FDA reports)
SINUS DISORDER ( 2 FDA reports)
SKIN DISORDER ( 2 FDA reports)
SKIN HYPERPIGMENTATION ( 2 FDA reports)
SPINAL COLUMN STENOSIS ( 2 FDA reports)
SUICIDAL BEHAVIOUR ( 2 FDA reports)
SWELLING FACE ( 2 FDA reports)
THYROID DISORDER ( 2 FDA reports)
TOE DEFORMITY ( 2 FDA reports)
TOOTH DISORDER ( 2 FDA reports)
TREATMENT NONCOMPLIANCE ( 2 FDA reports)
TRICUSPID VALVE INCOMPETENCE ( 2 FDA reports)
ULCER ( 2 FDA reports)
UTERINE LEIOMYOMA ( 2 FDA reports)
VENTRICULAR HYPERTROPHY ( 2 FDA reports)
VERTEBRAL FORAMINAL STENOSIS ( 2 FDA reports)
VIRAL UPPER RESPIRATORY TRACT INFECTION ( 2 FDA reports)
VOMITING ( 2 FDA reports)
VULVOVAGINAL DISCOMFORT ( 2 FDA reports)
VULVOVAGINAL MYCOTIC INFECTION ( 2 FDA reports)
WEIGHT INCREASED ( 2 FDA reports)
ABDOMINAL PAIN ( 1 FDA reports)
AKINESIA ( 1 FDA reports)
ARACHNOID CYST ( 1 FDA reports)
ARTHROPATHY ( 1 FDA reports)
ASTHENIA ( 1 FDA reports)
BACK DISORDER ( 1 FDA reports)
BLISTER ( 1 FDA reports)
BLOOD GLUCOSE INCREASED ( 1 FDA reports)
CARDIOVASCULAR DISORDER ( 1 FDA reports)
CELLULITIS ( 1 FDA reports)
CERUMEN IMPACTION ( 1 FDA reports)
COMMINUTED FRACTURE ( 1 FDA reports)
COUGH ( 1 FDA reports)
DEATH ( 1 FDA reports)
DERMATOMYOSITIS ( 1 FDA reports)
DIABETES MELLITUS ( 1 FDA reports)
DISSOCIATION ( 1 FDA reports)
DIVERTICULUM ( 1 FDA reports)
DYSPHAGIA ( 1 FDA reports)
DYSSTASIA ( 1 FDA reports)
DYSTHYMIC DISORDER ( 1 FDA reports)
DYSURIA ( 1 FDA reports)
EMOTIONAL DISORDER ( 1 FDA reports)
EXOSTOSIS ( 1 FDA reports)
FACIAL PALSY ( 1 FDA reports)
FAT NECROSIS ( 1 FDA reports)
FEELING ABNORMAL ( 1 FDA reports)
GAIT DISTURBANCE ( 1 FDA reports)
GINGIVITIS ( 1 FDA reports)
HAEMOGLOBIN DECREASED ( 1 FDA reports)
HALLUCINATION ( 1 FDA reports)
HEMIANOPIA HETERONYMOUS ( 1 FDA reports)
HEMIPLEGIA ( 1 FDA reports)
HEPATIC STEATOSIS ( 1 FDA reports)
HERPES SIMPLEX ( 1 FDA reports)
HERPES ZOSTER ( 1 FDA reports)
HYPERKERATOSIS ( 1 FDA reports)
HYPERSENSITIVITY ( 1 FDA reports)
HYPOGLYCAEMIA ( 1 FDA reports)
INCOHERENT ( 1 FDA reports)
INCREASED UPPER AIRWAY SECRETION ( 1 FDA reports)
INFECTION ( 1 FDA reports)
INFLAMMATION ( 1 FDA reports)
INFLUENZA ( 1 FDA reports)
INJECTION SITE PRURITUS ( 1 FDA reports)
LABORATORY TEST INTERFERENCE ( 1 FDA reports)
LIGAMENT DISORDER ( 1 FDA reports)
LYMPHADENOPATHY ( 1 FDA reports)
MALAISE ( 1 FDA reports)
MEDICAL DEVICE COMPLICATION ( 1 FDA reports)
MEDICATION ERROR ( 1 FDA reports)
MENTAL IMPAIRMENT ( 1 FDA reports)
MYALGIA ( 1 FDA reports)
NERVE COMPRESSION ( 1 FDA reports)
OPTIC NERVE DISORDER ( 1 FDA reports)
OROPHARYNGEAL PAIN ( 1 FDA reports)
OSTEOPOROSIS ( 1 FDA reports)
PAIN ( 1 FDA reports)
PELVIC NEOPLASM ( 1 FDA reports)
PNEUMONIA ( 1 FDA reports)
PRESCRIBED OVERDOSE ( 1 FDA reports)
PSYCHOMOTOR HYPERACTIVITY ( 1 FDA reports)
RASH ( 1 FDA reports)
RED BLOOD CELL SEDIMENTATION RATE INCREASED ( 1 FDA reports)
REFUSAL OF TREATMENT BY RELATIVE ( 1 FDA reports)
RESPIRATORY DISTRESS ( 1 FDA reports)
SCOLIOSIS ( 1 FDA reports)
SEASONAL ALLERGY ( 1 FDA reports)
SELF ESTEEM DECREASED ( 1 FDA reports)
SENSATION OF FOREIGN BODY ( 1 FDA reports)
SKIN INFECTION ( 1 FDA reports)
SKIN LACERATION ( 1 FDA reports)
STAPHYLOCOCCAL INFECTION ( 1 FDA reports)
STEVENS-JOHNSON SYNDROME ( 1 FDA reports)
SUBCUTANEOUS ABSCESS ( 1 FDA reports)
SUBCUTANEOUS NODULE ( 1 FDA reports)
SYNCOPE ( 1 FDA reports)
TEMPORAL ARTERITIS ( 1 FDA reports)
THINKING ABNORMAL ( 1 FDA reports)
UNEVALUABLE EVENT ( 1 FDA reports)
UPPER RESPIRATORY TRACT INFECTION ( 1 FDA reports)
URINARY TRACT INFECTION ( 1 FDA reports)
VENTRICULAR DYSFUNCTION ( 1 FDA reports)
WHEEZING ( 1 FDA reports)
WRONG DRUG ADMINISTERED ( 1 FDA reports)

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