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MULTIPLE SCLEROSIS ( 8 FDA reports)
ABDOMINAL PAIN ( 5 FDA reports)
CONDITION AGGRAVATED ( 5 FDA reports)
NAUSEA ( 4 FDA reports)
CONSTIPATION ( 3 FDA reports)
DIZZINESS ( 3 FDA reports)
HEADACHE ( 3 FDA reports)
HYPERHIDROSIS ( 3 FDA reports)
INJECTION SITE ERYTHEMA ( 3 FDA reports)
MEDICATION ERROR ( 3 FDA reports)
OEDEMA PERIPHERAL ( 3 FDA reports)
VOMITING ( 3 FDA reports)
ANGINA PECTORIS ( 2 FDA reports)
ARTHRITIS ( 2 FDA reports)
ASTHENIA ( 2 FDA reports)
ASTHMA ( 2 FDA reports)
CEREBROVASCULAR ACCIDENT ( 2 FDA reports)
CHILLS ( 2 FDA reports)
CHOLECYSTECTOMY ( 2 FDA reports)
DECREASED APPETITE ( 2 FDA reports)
DIFFICULTY IN WALKING ( 2 FDA reports)
DRUG INEFFECTIVE ( 2 FDA reports)
EPILEPSY ( 2 FDA reports)
HAEMOLYTIC ANAEMIA ( 2 FDA reports)
HEART RATE INCREASED ( 2 FDA reports)
INJECTION SITE INFECTION ( 2 FDA reports)
INJECTION SITE ULCER ( 2 FDA reports)
LEUKOPENIA ( 2 FDA reports)
MENIERE'S DISEASE ( 2 FDA reports)
MYALGIA ( 2 FDA reports)
PAIN ( 2 FDA reports)
PANCREATITIS ( 2 FDA reports)
PNEUMONIA ( 2 FDA reports)
RASH ERYTHEMATOUS ( 2 FDA reports)
RESPIRATORY ARREST ( 2 FDA reports)
RESPIRATORY FAILURE ( 2 FDA reports)
SPEECH DISORDER ( 2 FDA reports)
AGITATION ( 1 FDA reports)
ANAEMIA ( 1 FDA reports)
ANOREXIA ( 1 FDA reports)
APPLICATION SITE ERYTHEMA ( 1 FDA reports)
APPLICATION SITE IRRITATION ( 1 FDA reports)
APPLICATION SITE PAIN ( 1 FDA reports)
ARRHYTHMIA ( 1 FDA reports)
ARTERIAL DISORDER ( 1 FDA reports)
ARTERIAL OCCLUSIVE DISEASE ( 1 FDA reports)
AUTOIMMUNE HEPATITIS ( 1 FDA reports)
BACK PAIN ( 1 FDA reports)
BLOOD CHOLESTEROL INCREASED ( 1 FDA reports)
BLOOD GLUCOSE DECREASED ( 1 FDA reports)
BLOOD PRESSURE INCREASED ( 1 FDA reports)
BLOOD SODIUM DECREASED ( 1 FDA reports)
BLOOD THYROID STIMULATING HORMONE DECREASED ( 1 FDA reports)
BLOOD TRIGLYCERIDES INCREASED ( 1 FDA reports)
BRAIN SCAN ABNORMAL ( 1 FDA reports)
BRONCHOSTENOSIS ( 1 FDA reports)
CARDIAC ARREST ( 1 FDA reports)
CARDIOMEGALY ( 1 FDA reports)
CHEST DISCOMFORT ( 1 FDA reports)
CHEST PAIN ( 1 FDA reports)
CHOLECYSTITIS ( 1 FDA reports)
COLD SWEAT ( 1 FDA reports)
CONFUSIONAL STATE ( 1 FDA reports)
CONTUSION ( 1 FDA reports)
CONVULSION ( 1 FDA reports)
DEEP VEIN THROMBOSIS ( 1 FDA reports)
DEHYDRATION ( 1 FDA reports)
DEPRESSED LEVEL OF CONSCIOUSNESS ( 1 FDA reports)
DEPRESSION SUICIDAL ( 1 FDA reports)
DIABETES INSIPIDUS ( 1 FDA reports)
DIABETIC KETOACIDOSIS ( 1 FDA reports)
DIARRHOEA ( 1 FDA reports)
DRUG DOSE OMISSION ( 1 FDA reports)
DRUG HYPERSENSITIVITY ( 1 FDA reports)
DRY EYE ( 1 FDA reports)
DYSGRAPHIA ( 1 FDA reports)
DYSKINESIA ( 1 FDA reports)
DYSPNOEA ( 1 FDA reports)
DYSPNOEA EXACERBATED ( 1 FDA reports)
EATING DISORDER ( 1 FDA reports)
ENCEPHALOPATHY ( 1 FDA reports)
FEELING ABNORMAL ( 1 FDA reports)
GAIT DISTURBANCE ( 1 FDA reports)
HALLUCINATION, VISUAL ( 1 FDA reports)
HEPATIC FAILURE ( 1 FDA reports)
HYPERNATRAEMIA ( 1 FDA reports)
HYPERTENSION ( 1 FDA reports)
HYPOAESTHESIA ( 1 FDA reports)
HYPOKINESIA ( 1 FDA reports)
HYPOTHYROIDISM ( 1 FDA reports)
IMPAIRED DRIVING ABILITY ( 1 FDA reports)
INCREASED TENDENCY TO BRUISE ( 1 FDA reports)
INJECTION SITE ABSCESS ( 1 FDA reports)
INJECTION SITE CELLULITIS ( 1 FDA reports)
INJECTION SITE DESQUAMATION ( 1 FDA reports)
INJECTION SITE HAEMORRHAGE ( 1 FDA reports)
INJECTION SITE INFLAMMATION ( 1 FDA reports)
INJECTION SITE MASS ( 1 FDA reports)
INJECTION SITE NECROSIS ( 1 FDA reports)
INJECTION SITE PAIN ( 1 FDA reports)
INJECTION SITE PRURITUS ( 1 FDA reports)
INJECTION SITE RASH ( 1 FDA reports)
INJECTION SITE REACTION ( 1 FDA reports)
INSOMNIA ( 1 FDA reports)
LOSS OF CONSCIOUSNESS ( 1 FDA reports)
MALAISE ( 1 FDA reports)
MITRAL VALVE DISEASE ( 1 FDA reports)
MITRAL VALVE INCOMPETENCE ( 1 FDA reports)
MOTOR DYSFUNCTION ( 1 FDA reports)
MUCOUS MEMBRANE DISORDER ( 1 FDA reports)
MULTIPLE SCLEROSIS RELAPSE ( 1 FDA reports)
MUSCLE SPASMS ( 1 FDA reports)
MUSCULOSKELETAL DISORDER ( 1 FDA reports)
MUSCULOSKELETAL STIFFNESS ( 1 FDA reports)
NERVOUS SYSTEM DISORDER ( 1 FDA reports)
NON-SMALL CELL LUNG CANCER ( 1 FDA reports)
PAIN IN EXTREMITY ( 1 FDA reports)
PALPITATIONS ( 1 FDA reports)
PANIC ATTACK ( 1 FDA reports)
PARKINSON'S DISEASE ( 1 FDA reports)
PERIPHERAL COLDNESS ( 1 FDA reports)
PERIPHERAL VASCULAR DISORDER ( 1 FDA reports)
PIGMENTATION DISORDER ( 1 FDA reports)
PLEURAL DISORDER ( 1 FDA reports)
PNEUMOTHORAX ( 1 FDA reports)
POST PROCEDURAL PAIN ( 1 FDA reports)
PROGRESSIVE MULTIPLE SCLEROSIS ( 1 FDA reports)
PULMONARY EMBOLISM ( 1 FDA reports)
PULMONARY MASS ( 1 FDA reports)
PULSE ABSENT ( 1 FDA reports)
RASH MACULAR ( 1 FDA reports)
RECTAL HAEMORRHAGE ( 1 FDA reports)
REFUSAL OF TREATMENT BY PATIENT ( 1 FDA reports)
RENAL FAILURE ACUTE ( 1 FDA reports)
SCAB ( 1 FDA reports)
SKIN DISCOLOURATION ( 1 FDA reports)
SKIN DISORDER ( 1 FDA reports)
SLEEP APNOEA SYNDROME ( 1 FDA reports)
SPIDER NAEVUS ( 1 FDA reports)
SPLINTER HAEMORRHAGES ( 1 FDA reports)
STEREOTYPY ( 1 FDA reports)
STOMATITIS ( 1 FDA reports)
STRESS ( 1 FDA reports)
SUBCUTANEOUS EMPHYSEMA ( 1 FDA reports)
SUICIDAL IDEATION ( 1 FDA reports)
SYNCOPE ( 1 FDA reports)
THYROID DISORDER ( 1 FDA reports)
TREMOR ( 1 FDA reports)
UPPER RESPIRATORY TRACT CONGESTION ( 1 FDA reports)
URINARY RETENTION ( 1 FDA reports)
VASCULITIS ( 1 FDA reports)
VIRAL INFECTION ( 1 FDA reports)
VISION BLURRED ( 1 FDA reports)
WEIGHT INCREASED ( 1 FDA reports)
WHITE BLOOD CELL COUNT DECREASED ( 1 FDA reports)
XEROPHTHALMIA ( 1 FDA reports)

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