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

DYSPNOEA ( 9 FDA reports)
INFUSION RELATED REACTION ( 9 FDA reports)
PAIN IN EXTREMITY ( 8 FDA reports)
BACK PAIN ( 7 FDA reports)
SINUSITIS ( 7 FDA reports)
ANXIETY ( 6 FDA reports)
NAUSEA ( 6 FDA reports)
BLOOD POTASSIUM DECREASED ( 5 FDA reports)
BLOOD PRESSURE DECREASED ( 5 FDA reports)
DYSKINESIA ( 5 FDA reports)
ERYTHEMA ( 5 FDA reports)
FATIGUE ( 5 FDA reports)
OEDEMA PERIPHERAL ( 5 FDA reports)
PARALYSIS ( 5 FDA reports)
COUGH ( 4 FDA reports)
PAIN ( 4 FDA reports)
VOMITING ( 4 FDA reports)
ABDOMINAL PAIN UPPER ( 3 FDA reports)
APPLICATION SITE INFECTION ( 3 FDA reports)
APPLICATION SITE PAIN ( 3 FDA reports)
ARTHRALGIA ( 3 FDA reports)
CONSTIPATION ( 3 FDA reports)
DRUG INEFFECTIVE ( 3 FDA reports)
HYPERSENSITIVITY ( 3 FDA reports)
PHARYNGOLARYNGEAL PAIN ( 3 FDA reports)
ABNORMAL DREAMS ( 2 FDA reports)
ANGER ( 2 FDA reports)
APATHY ( 2 FDA reports)
ASTHMA ( 2 FDA reports)
BIPOLAR I DISORDER ( 2 FDA reports)
CHEST PAIN ( 2 FDA reports)
CONFUSIONAL STATE ( 2 FDA reports)
CRYING ( 2 FDA reports)
DYSPHAGIA ( 2 FDA reports)
EAR PAIN ( 2 FDA reports)
EMOTIONAL DISORDER ( 2 FDA reports)
EMOTIONAL DISTRESS ( 2 FDA reports)
EYE MOVEMENT DISORDER ( 2 FDA reports)
GALLBLADDER DISORDER ( 2 FDA reports)
HEADACHE ( 2 FDA reports)
INCORRECT DOSE ADMINISTERED ( 2 FDA reports)
INCREASED APPETITE ( 2 FDA reports)
INJURY ( 2 FDA reports)
INSOMNIA ( 2 FDA reports)
MALAISE ( 2 FDA reports)
MEDICAL DEVICE COMPLICATION ( 2 FDA reports)
MOOD SWINGS ( 2 FDA reports)
MYALGIA ( 2 FDA reports)
OFF LABEL USE ( 2 FDA reports)
PERSONALITY CHANGE ( 2 FDA reports)
POOR QUALITY SLEEP ( 2 FDA reports)
PRODUCT QUALITY ISSUE ( 2 FDA reports)
PRURITUS ( 2 FDA reports)
PSORIASIS ( 2 FDA reports)
PSYCHOMOTOR HYPERACTIVITY ( 2 FDA reports)
PYREXIA ( 2 FDA reports)
QUALITY OF LIFE DECREASED ( 2 FDA reports)
RASH ( 2 FDA reports)
RESTLESSNESS ( 2 FDA reports)
RHINITIS ( 2 FDA reports)
SCREAMING ( 2 FDA reports)
TIC ( 2 FDA reports)
URTICARIA ( 2 FDA reports)
VASCULAR ACCESS COMPLICATION ( 2 FDA reports)
WEIGHT INCREASED ( 2 FDA reports)
WRONG TECHNIQUE IN DRUG USAGE PROCESS ( 2 FDA reports)
ABDOMINAL DISTENSION ( 1 FDA reports)
ABNORMAL BEHAVIOUR ( 1 FDA reports)
ABSCESS ( 1 FDA reports)
ADVERSE REACTION ( 1 FDA reports)
AGGRESSION ( 1 FDA reports)
AGITATION ( 1 FDA reports)
ALOPECIA ( 1 FDA reports)
ANAPHYLACTOID REACTION ( 1 FDA reports)
ANHEDONIA ( 1 FDA reports)
AORTIC ANEURYSM ( 1 FDA reports)
APPENDICITIS PERFORATED ( 1 FDA reports)
APPLICATION SITE IRRITATION ( 1 FDA reports)
APPLICATION SITE PRURITUS ( 1 FDA reports)
ARTHRITIS ( 1 FDA reports)
ASTHENIA ( 1 FDA reports)
ATRIAL FIBRILLATION ( 1 FDA reports)
BREAST TENDERNESS ( 1 FDA reports)
CARDIAC ARREST ( 1 FDA reports)
CATARACT ( 1 FDA reports)
CHEILITIS ( 1 FDA reports)
CHEMICAL INJURY ( 1 FDA reports)
CHEST DISCOMFORT ( 1 FDA reports)
CHILLS ( 1 FDA reports)
CHOKING ( 1 FDA reports)
CHOLECYSTITIS CHRONIC ( 1 FDA reports)
COLECTOMY TOTAL ( 1 FDA reports)
COLITIS ISCHAEMIC ( 1 FDA reports)
COMPLETED SUICIDE ( 1 FDA reports)
CONDITION AGGRAVATED ( 1 FDA reports)
CONTRAST MEDIA REACTION ( 1 FDA reports)
CONVULSION ( 1 FDA reports)
DEATH ( 1 FDA reports)
DEPRESSION ( 1 FDA reports)
DIZZINESS ( 1 FDA reports)
DRUG DELIVERY SYSTEM MALFUNCTION ( 1 FDA reports)
DRUG DEPENDENCE ( 1 FDA reports)
DRUG DOSE OMISSION ( 1 FDA reports)
DRUG LEVEL INCREASED ( 1 FDA reports)
DYSPHONIA ( 1 FDA reports)
EAR INFECTION ( 1 FDA reports)
EXTREMITY NECROSIS ( 1 FDA reports)
FEAR ( 1 FDA reports)
FEBRILE INFECTION ( 1 FDA reports)
FLUSHING ( 1 FDA reports)
GAIT DISTURBANCE ( 1 FDA reports)
GASTRIC DISORDER ( 1 FDA reports)
GASTROOESOPHAGEAL REFLUX DISEASE ( 1 FDA reports)
GENERAL PHYSICAL CONDITION ABNORMAL ( 1 FDA reports)
GENERAL PHYSICAL HEALTH DETERIORATION ( 1 FDA reports)
HEPARIN-INDUCED THROMBOCYTOPENIA ( 1 FDA reports)
HEPATIC STEATOSIS ( 1 FDA reports)
HERNIA ( 1 FDA reports)
HYPERHIDROSIS ( 1 FDA reports)
HYPOTENSION ( 1 FDA reports)
ILEOSTOMY ( 1 FDA reports)
INJECTION SITE NODULE ( 1 FDA reports)
INJECTION SITE PAIN ( 1 FDA reports)
INJURY ASPHYXIATION ( 1 FDA reports)
IRRITABILITY ( 1 FDA reports)
JOINT SWELLING ( 1 FDA reports)
LIP SWELLING ( 1 FDA reports)
MENSTRUATION IRREGULAR ( 1 FDA reports)
MICTURITION URGENCY ( 1 FDA reports)
MULTI-ORGAN FAILURE ( 1 FDA reports)
MULTIPLE SCLEROSIS ( 1 FDA reports)
MUSCLE ATROPHY ( 1 FDA reports)
MUSCULOSKELETAL STIFFNESS ( 1 FDA reports)
MYOGLOBIN BLOOD PRESENT ( 1 FDA reports)
NO ADVERSE EVENT ( 1 FDA reports)
OCULAR HYPERAEMIA ( 1 FDA reports)
ORAL MUCOSAL EXFOLIATION ( 1 FDA reports)
PALLOR ( 1 FDA reports)
PALPITATIONS ( 1 FDA reports)
PARAESTHESIA ( 1 FDA reports)
PHARYNGEAL OEDEMA ( 1 FDA reports)
PNEUMONIA ( 1 FDA reports)
PNEUMONIA ASPIRATION ( 1 FDA reports)
PNEUMOTHORAX ( 1 FDA reports)
POST PROCEDURAL HAEMATOMA ( 1 FDA reports)
PRESYNCOPE ( 1 FDA reports)
PSYCHOLOGICAL TRAUMA ( 1 FDA reports)
PULMONARY FUNCTION TEST DECREASED ( 1 FDA reports)
RED BLOOD CELL COUNT DECREASED ( 1 FDA reports)
RENAL FAILURE ( 1 FDA reports)
RESPIRATORY FAILURE ( 1 FDA reports)
SENSITIVITY OF TEETH ( 1 FDA reports)
SENSORY DISTURBANCE ( 1 FDA reports)
SLEEP DISORDER ( 1 FDA reports)
SOMNOLENCE ( 1 FDA reports)
SUICIDAL IDEATION ( 1 FDA reports)
SWELLING FACE ( 1 FDA reports)
SWOLLEN TONGUE ( 1 FDA reports)
SYNCOPE ( 1 FDA reports)
THROMBOSIS ( 1 FDA reports)
THYROXINE FREE INCREASED ( 1 FDA reports)
TOOTHACHE ( 1 FDA reports)
TRIGGER FINGER ( 1 FDA reports)
TYPE 2 DIABETES MELLITUS ( 1 FDA reports)
UNEVALUABLE EVENT ( 1 FDA reports)
VAGINAL INFECTION ( 1 FDA reports)
VENTRICULAR TACHYCARDIA ( 1 FDA reports)
WEIGHT DECREASED ( 1 FDA reports)

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