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

HEADACHE ( 12 FDA reports)
NAUSEA ( 9 FDA reports)
OEDEMA PERIPHERAL ( 8 FDA reports)
PAIN ( 8 FDA reports)
COGNITIVE DISORDER ( 7 FDA reports)
ARTHRALGIA ( 6 FDA reports)
CONVULSION ( 5 FDA reports)
FATIGUE ( 5 FDA reports)
INAPPROPRIATE SCHEDULE OF DRUG ADMINISTRATION ( 5 FDA reports)
SKIN DISCOLOURATION ( 5 FDA reports)
ASTHENIA ( 4 FDA reports)
BLOOD PRESSURE INCREASED ( 4 FDA reports)
CHRONIC OBSTRUCTIVE PULMONARY DISEASE ( 4 FDA reports)
CYANOSIS ( 4 FDA reports)
DEHYDRATION ( 4 FDA reports)
DEPRESSION ( 4 FDA reports)
FIBROMYALGIA ( 4 FDA reports)
INJECTION SITE HAEMATOMA ( 4 FDA reports)
MALAISE ( 4 FDA reports)
MULTIPLE SCLEROSIS ( 4 FDA reports)
POSTERIOR REVERSIBLE ENCEPHALOPATHY SYNDROME ( 4 FDA reports)
RESPIRATORY ARREST ( 4 FDA reports)
VITAMIN B12 DEFICIENCY ( 4 FDA reports)
ANXIETY ( 3 FDA reports)
APPARENT DEATH ( 3 FDA reports)
BACK PAIN ( 3 FDA reports)
BLINDNESS ( 3 FDA reports)
CEREBRAL THROMBOSIS ( 3 FDA reports)
CONTUSION ( 3 FDA reports)
CORONARY ARTERY DISEASE ( 3 FDA reports)
COUGH ( 3 FDA reports)
DRUG WITHDRAWAL SYNDROME ( 3 FDA reports)
DYSKINESIA ( 3 FDA reports)
DYSLIPIDAEMIA ( 3 FDA reports)
DYSPHONIA ( 3 FDA reports)
FALL ( 3 FDA reports)
HAEMATEMESIS ( 3 FDA reports)
INJECTION SITE PAIN ( 3 FDA reports)
INSOMNIA ( 3 FDA reports)
INTERVERTEBRAL DISC PROTRUSION ( 3 FDA reports)
MEMORY IMPAIRMENT ( 3 FDA reports)
MICTURITION URGENCY ( 3 FDA reports)
OVERDOSE ( 3 FDA reports)
PAIN IN EXTREMITY ( 3 FDA reports)
QUADRIPARESIS ( 3 FDA reports)
SENSATION OF HEAVINESS ( 3 FDA reports)
SUICIDAL IDEATION ( 3 FDA reports)
WEIGHT DECREASED ( 3 FDA reports)
WRONG TECHNIQUE IN DRUG USAGE PROCESS ( 3 FDA reports)
ABDOMINAL PAIN UPPER ( 2 FDA reports)
ANOREXIA ( 2 FDA reports)
BLINDNESS UNILATERAL ( 2 FDA reports)
CHILLS ( 2 FDA reports)
COMPLETED SUICIDE ( 2 FDA reports)
CONFUSIONAL STATE ( 2 FDA reports)
DECREASED APPETITE ( 2 FDA reports)
DIARRHOEA ( 2 FDA reports)
DIZZINESS ( 2 FDA reports)
DRUG INEFFECTIVE ( 2 FDA reports)
DYSPNOEA ( 2 FDA reports)
ENTEROCOLITIS HAEMORRHAGIC ( 2 FDA reports)
EXOSTOSIS ( 2 FDA reports)
FEELING JITTERY ( 2 FDA reports)
FLUSHING ( 2 FDA reports)
FORMICATION ( 2 FDA reports)
GASTROINTESTINAL TRACT ADENOMA ( 2 FDA reports)
HOSPITALISATION ( 2 FDA reports)
INFLUENZA ( 2 FDA reports)
INFUSION RELATED REACTION ( 2 FDA reports)
INJECTION SITE URTICARIA ( 2 FDA reports)
INTERNATIONAL NORMALISED RATIO INCREASED ( 2 FDA reports)
IRRITABILITY ( 2 FDA reports)
JOINT RANGE OF MOTION DECREASED ( 2 FDA reports)
JOINT SWELLING ( 2 FDA reports)
LIP DISCOLOURATION ( 2 FDA reports)
MEDICATION ERROR ( 2 FDA reports)
MOUTH ULCERATION ( 2 FDA reports)
NECK PAIN ( 2 FDA reports)
PNEUMONIA ( 2 FDA reports)
POLYP ( 2 FDA reports)
PROTHROMBIN TIME PROLONGED ( 2 FDA reports)
TENDON INJURY ( 2 FDA reports)
TREMOR ( 2 FDA reports)
VENOUS OCCLUSION ( 2 FDA reports)
WEIGHT INCREASED ( 2 FDA reports)
ABDOMINAL PAIN ( 1 FDA reports)
ACUTE PULMONARY OEDEMA ( 1 FDA reports)
ADVERSE DRUG REACTION ( 1 FDA reports)
AGEUSIA ( 1 FDA reports)
AGGRESSION ( 1 FDA reports)
AGITATION ( 1 FDA reports)
AMNESIA ( 1 FDA reports)
APPARENT LIFE THREATENING EVENT ( 1 FDA reports)
APPETITE DISORDER ( 1 FDA reports)
ASTHMA ( 1 FDA reports)
AXILLARY PAIN ( 1 FDA reports)
BALANCE DISORDER ( 1 FDA reports)
BLISTER ( 1 FDA reports)
BLOOD CALCIUM DECREASED ( 1 FDA reports)
BLOOD CHLORIDE DECREASED ( 1 FDA reports)
BLOOD CHOLESTEROL INCREASED ( 1 FDA reports)
BLOOD CREATINE DECREASED ( 1 FDA reports)
BLOOD GLUCOSE INCREASED ( 1 FDA reports)
BLOOD POTASSIUM INCREASED ( 1 FDA reports)
BLOOD PRESSURE SYSTOLIC INCREASED ( 1 FDA reports)
BLOOD SODIUM DECREASED ( 1 FDA reports)
BLOOD UREA INCREASED ( 1 FDA reports)
BREAST PAIN ( 1 FDA reports)
BURKITT'S LYMPHOMA ( 1 FDA reports)
BURNING SENSATION ( 1 FDA reports)
CARDIAC ARREST ( 1 FDA reports)
CARPAL TUNNEL SYNDROME ( 1 FDA reports)
CENTRAL NERVOUS SYSTEM LESION ( 1 FDA reports)
CEREBROVASCULAR ACCIDENT ( 1 FDA reports)
CHEST PAIN ( 1 FDA reports)
CHOLELITHIASIS ( 1 FDA reports)
COLD SWEAT ( 1 FDA reports)
COLONIC POLYP ( 1 FDA reports)
CONDITION AGGRAVATED ( 1 FDA reports)
CROHN'S DISEASE ( 1 FDA reports)
DEHYDROEPIANDROSTERONE INCREASED ( 1 FDA reports)
DEPRESSED LEVEL OF CONSCIOUSNESS ( 1 FDA reports)
DERMATOMYOSITIS ( 1 FDA reports)
DISEASE RECURRENCE ( 1 FDA reports)
DISORIENTATION ( 1 FDA reports)
DRUG DOSE OMISSION ( 1 FDA reports)
DRUG HYPERSENSITIVITY ( 1 FDA reports)
DRY MOUTH ( 1 FDA reports)
DYSPEPSIA ( 1 FDA reports)
DYSPHAGIA ( 1 FDA reports)
ECONOMIC PROBLEM ( 1 FDA reports)
EPILEPSY ( 1 FDA reports)
ERYTHEMA ( 1 FDA reports)
EXCORIATION ( 1 FDA reports)
FACIAL PALSY ( 1 FDA reports)
FEELING HOT ( 1 FDA reports)
GAIT DISTURBANCE ( 1 FDA reports)
GASTROOESOPHAGEAL REFLUX DISEASE ( 1 FDA reports)
GENITAL INFECTION BACTERIAL ( 1 FDA reports)
HEPATIC FUNCTION ABNORMAL ( 1 FDA reports)
HEPATITIS ( 1 FDA reports)
HIRSUTISM ( 1 FDA reports)
HYPERHIDROSIS ( 1 FDA reports)
HYPERPHAGIA ( 1 FDA reports)
HYPERSOMNIA ( 1 FDA reports)
HYPOKALAEMIA ( 1 FDA reports)
HYPOKINESIA ( 1 FDA reports)
HYPOTHALAMO-PITUITARY DISORDERS ( 1 FDA reports)
HYPOXIA ( 1 FDA reports)
IMPLANT SITE REACTION ( 1 FDA reports)
INCORRECT DOSE ADMINISTERED ( 1 FDA reports)
INCREASED TENDENCY TO BRUISE ( 1 FDA reports)
INFLUENZA LIKE ILLNESS ( 1 FDA reports)
INJECTION SITE ERYTHEMA ( 1 FDA reports)
INJECTION SITE INDURATION ( 1 FDA reports)
INJECTION SITE REACTION ( 1 FDA reports)
INJECTION SITE SWELLING ( 1 FDA reports)
INJECTION SITE WARMTH ( 1 FDA reports)
INJURY ( 1 FDA reports)
INTERNATIONAL NORMALISED RATIO DECREASED ( 1 FDA reports)
LOGORRHOEA ( 1 FDA reports)
LOSS OF CONSCIOUSNESS ( 1 FDA reports)
LUNG CANCER METASTATIC ( 1 FDA reports)
LUNG DISORDER ( 1 FDA reports)
MALNUTRITION ( 1 FDA reports)
MUCOSAL INFLAMMATION ( 1 FDA reports)
MULTIPLE SCLEROSIS RELAPSE ( 1 FDA reports)
MUSCLE RIGIDITY ( 1 FDA reports)
MUSCLE SPASMS ( 1 FDA reports)
MUSCLE TWITCHING ( 1 FDA reports)
MUSCULAR WEAKNESS ( 1 FDA reports)
MUSCULOSKELETAL DISORDER ( 1 FDA reports)
MYOCARDIAL INFARCTION ( 1 FDA reports)
MYOCLONUS ( 1 FDA reports)
MYOSITIS ( 1 FDA reports)
NEPHROLITHIASIS ( 1 FDA reports)
NEUROPATHY PERIPHERAL ( 1 FDA reports)
NEUTROPENIA ( 1 FDA reports)
NIGHTMARE ( 1 FDA reports)
OFF LABEL USE ( 1 FDA reports)
ORAL CANDIDIASIS ( 1 FDA reports)
OROPHARYNGEAL PAIN ( 1 FDA reports)
PAIN IN JAW ( 1 FDA reports)
PARAESTHESIA ( 1 FDA reports)
PHARYNGOLARYNGEAL PAIN ( 1 FDA reports)
PRODUCTIVE COUGH ( 1 FDA reports)
PROSTATE CANCER ( 1 FDA reports)
PRURITUS ( 1 FDA reports)
PULMONARY ARTERY DILATATION ( 1 FDA reports)
PURULENT DISCHARGE ( 1 FDA reports)
PYREXIA ( 1 FDA reports)
RECTAL HAEMORRHAGE ( 1 FDA reports)
RED BLOOD CELLS CSF POSITIVE ( 1 FDA reports)
ROAD TRAFFIC ACCIDENT ( 1 FDA reports)
RUPTURED CEREBRAL ANEURYSM ( 1 FDA reports)
SECONDARY HYPOGONADISM ( 1 FDA reports)
SEPSIS ( 1 FDA reports)
SKIN BURNING SENSATION ( 1 FDA reports)
SKIN NODULE ( 1 FDA reports)
SKIN SWELLING ( 1 FDA reports)
SPEECH DISORDER ( 1 FDA reports)
STAPHYLOCOCCAL INFECTION ( 1 FDA reports)
STOMACH DISCOMFORT ( 1 FDA reports)
THROMBOCYTOPENIA ( 1 FDA reports)
VASCULITIS ( 1 FDA reports)
VISION BLURRED ( 1 FDA reports)
VOMITING ( 1 FDA reports)
WOUND ( 1 FDA reports)

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