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

PAIN ( 21 FDA reports)
ABDOMINAL PAIN UPPER ( 18 FDA reports)
BACK PAIN ( 18 FDA reports)
DEPRESSION ( 18 FDA reports)
ANXIETY ( 17 FDA reports)
FEAR ( 17 FDA reports)
NERVOUSNESS ( 17 FDA reports)
TREMOR ( 17 FDA reports)
DYSPNOEA ( 16 FDA reports)
SUICIDAL IDEATION ( 15 FDA reports)
PAIN IN EXTREMITY ( 14 FDA reports)
ERYTHEMA ( 12 FDA reports)
HEADACHE ( 12 FDA reports)
INSOMNIA ( 12 FDA reports)
CHILLS ( 11 FDA reports)
PANIC REACTION ( 11 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 10 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 10 FDA reports)
BRUXISM ( 10 FDA reports)
IMPATIENCE ( 10 FDA reports)
INJECTION SITE DISCOLOURATION ( 10 FDA reports)
INJECTION SITE ERYTHEMA ( 10 FDA reports)
INJECTION SITE HAEMORRHAGE ( 10 FDA reports)
INJECTION SITE PAIN ( 10 FDA reports)
INJECTION SITE RASH ( 10 FDA reports)
IRRITABILITY ( 10 FDA reports)
MALAISE ( 10 FDA reports)
MENSTRUAL DISORDER ( 10 FDA reports)
MULTIPLE SCLEROSIS RELAPSE ( 10 FDA reports)
NEGATIVE THOUGHTS ( 10 FDA reports)
NIGHTMARE ( 10 FDA reports)
PNEUMONIA ( 10 FDA reports)
SENSATION OF HEAVINESS ( 10 FDA reports)
TENSION ( 10 FDA reports)
VAGINAL DISCHARGE ( 10 FDA reports)
VAGINAL HAEMORRHAGE ( 10 FDA reports)
FEELING ABNORMAL ( 9 FDA reports)
CRYING ( 8 FDA reports)
PANIC DISORDER ( 8 FDA reports)
SKIN HAEMORRHAGE ( 8 FDA reports)
GASTRITIS ( 7 FDA reports)
MUSCLE SPASMS ( 7 FDA reports)
STRESS ( 7 FDA reports)
VISION BLURRED ( 7 FDA reports)
ACNE ( 6 FDA reports)
DISTURBANCE IN ATTENTION ( 6 FDA reports)
INJURY ASSOCIATED WITH DEVICE ( 6 FDA reports)
IRRITABLE BOWEL SYNDROME ( 6 FDA reports)
LABYRINTHITIS ( 6 FDA reports)
SEBORRHOEA ( 6 FDA reports)
AFFECT LABILITY ( 5 FDA reports)
ANAEMIA ( 5 FDA reports)
ANOGENITAL WARTS ( 5 FDA reports)
ARTHRALGIA ( 5 FDA reports)
ASTHENIA ( 5 FDA reports)
BLINDNESS ( 5 FDA reports)
BREAST PAIN ( 5 FDA reports)
CHEST PAIN ( 5 FDA reports)
COLITIS EROSIVE ( 5 FDA reports)
GASTRIC POLYPS ( 5 FDA reports)
HAIR COLOUR CHANGES ( 5 FDA reports)
HEAD DISCOMFORT ( 5 FDA reports)
NEPHROLITHIASIS ( 5 FDA reports)
RASH ( 5 FDA reports)
RENAL FAILURE ( 5 FDA reports)
SKIN PAPILLOMA ( 5 FDA reports)
VARICOSE VEIN ( 5 FDA reports)
WEIGHT INCREASED ( 5 FDA reports)
BLOOD PRESSURE INCREASED ( 4 FDA reports)
BONE DISORDER ( 4 FDA reports)
CARDIAC DISORDER ( 4 FDA reports)
CARDIAC FAILURE CONGESTIVE ( 4 FDA reports)
CHRONIC OBSTRUCTIVE PULMONARY DISEASE ( 4 FDA reports)
GASTROOESOPHAGEAL REFLUX DISEASE ( 4 FDA reports)
HYPERTENSION ( 4 FDA reports)
HYPOAESTHESIA ( 4 FDA reports)
HYPOMENORRHOEA ( 4 FDA reports)
ILEITIS ( 4 FDA reports)
INTERVERTEBRAL DISC PROTRUSION ( 4 FDA reports)
LIBIDO DECREASED ( 4 FDA reports)
LOSS OF CONSCIOUSNESS ( 4 FDA reports)
MEMORY IMPAIRMENT ( 4 FDA reports)
MOOD ALTERED ( 4 FDA reports)
MUSCLE TIGHTNESS ( 4 FDA reports)
OEDEMA PERIPHERAL ( 4 FDA reports)
OESOPHAGITIS ( 4 FDA reports)
PALPITATIONS ( 4 FDA reports)
PEAU D'ORANGE ( 4 FDA reports)
PREMENSTRUAL SYNDROME ( 4 FDA reports)
PYREXIA ( 4 FDA reports)
RENAL FAILURE CHRONIC ( 4 FDA reports)
SKIN WRINKLING ( 4 FDA reports)
SUPERFICIAL VEIN PROMINENCE ( 4 FDA reports)
TACHYCARDIA ( 4 FDA reports)
ACUTE PULMONARY OEDEMA ( 3 FDA reports)
AGITATION ( 3 FDA reports)
BRONCHITIS ACUTE ( 3 FDA reports)
CANDIDIASIS ( 3 FDA reports)
CARDIOMEGALY ( 3 FDA reports)
CATARACT ( 3 FDA reports)
CEREBROVASCULAR ACCIDENT ( 3 FDA reports)
COLITIS ( 3 FDA reports)
CONVULSION ( 3 FDA reports)
COUGH ( 3 FDA reports)
DIVERTICULUM ( 3 FDA reports)
DYSKINESIA ( 3 FDA reports)
DYSPEPSIA ( 3 FDA reports)
DYSPHONIA ( 3 FDA reports)
EMPHYSEMA ( 3 FDA reports)
EYE DISORDER ( 3 FDA reports)
FALL ( 3 FDA reports)
FATIGUE ( 3 FDA reports)
FLUID OVERLOAD ( 3 FDA reports)
GAIT DISTURBANCE ( 3 FDA reports)
GASTROINTESTINAL DISORDER ( 3 FDA reports)
HAEMORRHOIDS ( 3 FDA reports)
HYPERKALAEMIA ( 3 FDA reports)
HYPOPHAGIA ( 3 FDA reports)
LETHARGY ( 3 FDA reports)
LUNG CONSOLIDATION ( 3 FDA reports)
LUPUS NEPHRITIS ( 3 FDA reports)
MICTURITION DISORDER ( 3 FDA reports)
MUSCULOSKELETAL CHEST PAIN ( 3 FDA reports)
MUSCULOSKELETAL PAIN ( 3 FDA reports)
MYOCARDIAL INFARCTION ( 3 FDA reports)
NEUROPATHY PERIPHERAL ( 3 FDA reports)
OCCULT BLOOD POSITIVE ( 3 FDA reports)
OESOPHAGEAL CANDIDIASIS ( 3 FDA reports)
ORCHITIS ( 3 FDA reports)
PINGUECULA ( 3 FDA reports)
PRESCRIBED OVERDOSE ( 3 FDA reports)
RETINOPATHY HYPERTENSIVE ( 3 FDA reports)
SEPSIS ( 3 FDA reports)
STAPHYLOCOCCAL INFECTION ( 3 FDA reports)
SYNCOPE ( 3 FDA reports)
SYSTEMIC LUPUS ERYTHEMATOSUS ( 3 FDA reports)
TREATMENT NONCOMPLIANCE ( 3 FDA reports)
URINARY INCONTINENCE ( 3 FDA reports)
URINARY TRACT INFECTION ( 3 FDA reports)
UVEITIS ( 3 FDA reports)
CHEST DISCOMFORT ( 2 FDA reports)
COMA ( 2 FDA reports)
CORONARY ARTERY DISEASE ( 2 FDA reports)
DEPRESSED MOOD ( 2 FDA reports)
DIARRHOEA ( 2 FDA reports)
DRUG EFFECT DECREASED ( 2 FDA reports)
DRUG INEFFECTIVE ( 2 FDA reports)
DRY MOUTH ( 2 FDA reports)
EXPOSURE TO TOXIC AGENT ( 2 FDA reports)
EYE PAIN ( 2 FDA reports)
FORMICATION ( 2 FDA reports)
HEPATITIS ( 2 FDA reports)
HEPATOCELLULAR DAMAGE ( 2 FDA reports)
HYPERGLYCAEMIA ( 2 FDA reports)
INFECTION ( 2 FDA reports)
INJECTION SITE EXFOLIATION ( 2 FDA reports)
INTRAOCULAR PRESSURE TEST ABNORMAL ( 2 FDA reports)
OCULAR ICTERUS ( 2 FDA reports)
PERIPHERAL COLDNESS ( 2 FDA reports)
PRODUCTIVE COUGH ( 2 FDA reports)
RENAL FAILURE ACUTE ( 2 FDA reports)
SCRATCH ( 2 FDA reports)
SHOCK ( 2 FDA reports)
SKIN DISORDER ( 2 FDA reports)
SKIN INJURY ( 2 FDA reports)
SOMNOLENCE ( 2 FDA reports)
SPEECH DISORDER ( 2 FDA reports)
THROMBOSIS ( 2 FDA reports)
TONGUE BITING ( 2 FDA reports)
ULCER ( 2 FDA reports)
ABASIA ( 1 FDA reports)
ABDOMINAL DISCOMFORT ( 1 FDA reports)
ABDOMINAL DISTENSION ( 1 FDA reports)
ABDOMINAL PAIN ( 1 FDA reports)
ABORTION MISSED ( 1 FDA reports)
ACCOMMODATION DISORDER ( 1 FDA reports)
ACTIVITIES OF DAILY LIVING IMPAIRED ( 1 FDA reports)
AGGRESSION ( 1 FDA reports)
AGNOSIA ( 1 FDA reports)
ANGINA PECTORIS ( 1 FDA reports)
ANGINA UNSTABLE ( 1 FDA reports)
ANGIOPATHY ( 1 FDA reports)
ANOREXIA ( 1 FDA reports)
AORTIC VALVE INCOMPETENCE ( 1 FDA reports)
APHASIA ( 1 FDA reports)
ARRHYTHMIA ( 1 FDA reports)
ARTERIOSCLEROSIS CORONARY ARTERY ( 1 FDA reports)
ARTHRITIS ( 1 FDA reports)
ASEPTIC NECROSIS BONE ( 1 FDA reports)
ATELECTASIS ( 1 FDA reports)
BACTERAEMIA ( 1 FDA reports)
BLISTER ( 1 FDA reports)
BLOOD CHOLESTEROL INCREASED ( 1 FDA reports)
BLOOD GLUCOSE INCREASED ( 1 FDA reports)
BLOOD PRESSURE ABNORMAL ( 1 FDA reports)
BONE DEBRIDEMENT ( 1 FDA reports)
BONE TRIMMING ( 1 FDA reports)
BRAIN NEOPLASM ( 1 FDA reports)
BRAIN OPERATION ( 1 FDA reports)
BRONCHIAL HYPERREACTIVITY ( 1 FDA reports)
BRONCHITIS ( 1 FDA reports)
CARDIAC ARREST NEONATAL ( 1 FDA reports)
CAROTID ARTERY STENOSIS ( 1 FDA reports)
CARPAL TUNNEL SYNDROME ( 1 FDA reports)
CIRCUMSTANCE OR INFORMATION CAPABLE OF LEADING TO MEDICATION ERROR ( 1 FDA reports)
COAGULOPATHY ( 1 FDA reports)
CONFUSIONAL STATE ( 1 FDA reports)
CONSTIPATION ( 1 FDA reports)
COR PULMONALE ( 1 FDA reports)
DELIRIUM ( 1 FDA reports)
DERMATITIS EXFOLIATIVE ( 1 FDA reports)
DRUG DOSE OMISSION ( 1 FDA reports)
DRUG INTERACTION ( 1 FDA reports)
DRUG TOXICITY ( 1 FDA reports)
DYSGEUSIA ( 1 FDA reports)
DYSPHASIA ( 1 FDA reports)
EATING DISORDER ( 1 FDA reports)
EMOTIONAL DISTRESS ( 1 FDA reports)
EXCORIATION ( 1 FDA reports)
EXPIRED DRUG ADMINISTERED ( 1 FDA reports)
FACE OEDEMA ( 1 FDA reports)
FLATULENCE ( 1 FDA reports)
FRACTURE MALUNION ( 1 FDA reports)
GASTROINTESTINAL CANDIDIASIS ( 1 FDA reports)
GRAFT INFECTION ( 1 FDA reports)
HAEMODIALYSIS ( 1 FDA reports)
HALLUCINATION ( 1 FDA reports)
HEARING IMPAIRED ( 1 FDA reports)
HEART RATE ABNORMAL ( 1 FDA reports)
HEART RATE INCREASED ( 1 FDA reports)
HERPES VIRUS INFECTION ( 1 FDA reports)
HUMERUS FRACTURE ( 1 FDA reports)
HYPERSENSITIVITY ( 1 FDA reports)
HYPERTENSIVE CRISIS ( 1 FDA reports)
HYPOACUSIS ( 1 FDA reports)
HYPOTENSION ( 1 FDA reports)
HYPOXIA ( 1 FDA reports)
IMMOBILISATION PROLONGED ( 1 FDA reports)
IMMUNODEFICIENCY ( 1 FDA reports)
INCOHERENT ( 1 FDA reports)
INJECTION SITE MASS ( 1 FDA reports)
JOINT INJURY ( 1 FDA reports)
JOINT SWELLING ( 1 FDA reports)
LACRIMATION INCREASED ( 1 FDA reports)
LACTOSE INTOLERANCE ( 1 FDA reports)
LIVER DISORDER ( 1 FDA reports)
MICTURITION FREQUENCY DECREASED ( 1 FDA reports)
MITRAL VALVE INCOMPETENCE ( 1 FDA reports)
MUSCLE RIGIDITY ( 1 FDA reports)
MUSCLE TWITCHING ( 1 FDA reports)
MUSCULAR WEAKNESS ( 1 FDA reports)
MYALGIA ( 1 FDA reports)
NAUSEA ( 1 FDA reports)
NECK PAIN ( 1 FDA reports)
NEURALGIA ( 1 FDA reports)
OEDEMA ( 1 FDA reports)
OFF LABEL USE ( 1 FDA reports)
OSTEOPOROSIS ( 1 FDA reports)
PAIN OF SKIN ( 1 FDA reports)
PARTIAL SEIZURES ( 1 FDA reports)
PERICARDIAL EFFUSION ( 1 FDA reports)
PLEURAL EFFUSION ( 1 FDA reports)
POOR PERIPHERAL CIRCULATION ( 1 FDA reports)
PROSTHESIS USER ( 1 FDA reports)
PSORIASIS ( 1 FDA reports)
PSORIATIC ARTHROPATHY ( 1 FDA reports)
PTERYGIUM ( 1 FDA reports)
PULMONARY EMBOLISM ( 1 FDA reports)
RESPIRATORY FAILURE ( 1 FDA reports)
RETINAL HAEMORRHAGE ( 1 FDA reports)
SKIN DISCOLOURATION ( 1 FDA reports)
SKIN SWELLING ( 1 FDA reports)
SLEEP APNOEA SYNDROME ( 1 FDA reports)
STAPHYLOCOCCAL BACTERAEMIA ( 1 FDA reports)
SUICIDAL BEHAVIOUR ( 1 FDA reports)
SURGERY ( 1 FDA reports)
SWELLING FACE ( 1 FDA reports)
TINNITUS ( 1 FDA reports)
TOOTH EXTRACTION ( 1 FDA reports)
TRANSIENT ISCHAEMIC ATTACK ( 1 FDA reports)
TRICUSPID VALVE INCOMPETENCE ( 1 FDA reports)
URTICARIA ( 1 FDA reports)
VENTRICULAR HYPERTROPHY ( 1 FDA reports)
VENTRICULAR TACHYCARDIA ( 1 FDA reports)
VERTIGO ( 1 FDA reports)

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