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

ANXIETY ( 13 FDA reports)
HYPERTENSION ( 11 FDA reports)
BACK PAIN ( 10 FDA reports)
DIABETES MELLITUS ( 10 FDA reports)
DISORIENTATION ( 10 FDA reports)
HYPOMANIA ( 10 FDA reports)
MENTAL DISORDER ( 10 FDA reports)
MUSCULOSKELETAL PAIN ( 10 FDA reports)
MYOCARDIAL INFARCTION ( 10 FDA reports)
NEPHROLITHIASIS ( 10 FDA reports)
NEUROPATHY PERIPHERAL ( 10 FDA reports)
OEDEMA ( 10 FDA reports)
PALPITATIONS ( 10 FDA reports)
PANCREATITIS RELAPSING ( 10 FDA reports)
PARALYSIS ( 10 FDA reports)
BIPOLAR DISORDER ( 9 FDA reports)
HYPOAESTHESIA ( 9 FDA reports)
LOSS OF EMPLOYMENT ( 9 FDA reports)
POST-TRAUMATIC STRESS DISORDER ( 9 FDA reports)
BILE DUCT CANCER ( 7 FDA reports)
WEIGHT INCREASED ( 7 FDA reports)
APHONIA ( 6 FDA reports)
BLOOD GLUCOSE INCREASED ( 6 FDA reports)
NEOPLASM MALIGNANT ( 6 FDA reports)
PAPILLOMA VIRAL INFECTION ( 6 FDA reports)
CONFUSIONAL STATE ( 5 FDA reports)
DIZZINESS ( 5 FDA reports)
OEDEMA PERIPHERAL ( 5 FDA reports)
PAIN ( 5 FDA reports)
VAGINAL CANCER ( 5 FDA reports)
DYSPNOEA ( 4 FDA reports)
NAUSEA ( 4 FDA reports)
ROTATOR CUFF SYNDROME ( 4 FDA reports)
SWELLING ( 4 FDA reports)
ALOPECIA ( 3 FDA reports)
BREAST PAIN ( 3 FDA reports)
CEREBROVASCULAR ACCIDENT ( 3 FDA reports)
CONVULSION ( 3 FDA reports)
DIPLOPIA ( 3 FDA reports)
DRUG INEFFECTIVE ( 3 FDA reports)
DYSGEUSIA ( 3 FDA reports)
EPISTAXIS ( 3 FDA reports)
HYPERHIDROSIS ( 3 FDA reports)
INSOMNIA ( 3 FDA reports)
MENORRHAGIA ( 3 FDA reports)
MIGRAINE ( 3 FDA reports)
PARAESTHESIA ( 3 FDA reports)
RASH ( 3 FDA reports)
SENSATION OF HEAVINESS ( 3 FDA reports)
SUNBURN ( 3 FDA reports)
URINARY INCONTINENCE ( 3 FDA reports)
URINARY TRACT INFECTION ( 3 FDA reports)
AMNESIA ( 2 FDA reports)
ANAPHYLACTIC REACTION ( 2 FDA reports)
BLOOD PRESSURE DECREASED ( 2 FDA reports)
COMA ( 2 FDA reports)
CONSTIPATION ( 2 FDA reports)
CONTUSION ( 2 FDA reports)
DEPRESSION ( 2 FDA reports)
DRUG INTERACTION ( 2 FDA reports)
DRUG TOXICITY ( 2 FDA reports)
DRY SKIN ( 2 FDA reports)
DYSSTASIA ( 2 FDA reports)
FATIGUE ( 2 FDA reports)
GRAND MAL CONVULSION ( 2 FDA reports)
HIATUS HERNIA ( 2 FDA reports)
JOINT SWELLING ( 2 FDA reports)
LIGAMENT RUPTURE ( 2 FDA reports)
MYALGIA ( 2 FDA reports)
PHARYNGITIS ( 2 FDA reports)
PULMONARY EMBOLISM ( 2 FDA reports)
PYREXIA ( 2 FDA reports)
SPEECH DISORDER ( 2 FDA reports)
SYNCOPE ( 2 FDA reports)
UNEVALUABLE EVENT ( 2 FDA reports)
URINARY RETENTION ( 2 FDA reports)
VASOSPASM ( 2 FDA reports)
AGORAPHOBIA ( 1 FDA reports)
AKATHISIA ( 1 FDA reports)
APNOEA ( 1 FDA reports)
APPLICATION SITE IRRITATION ( 1 FDA reports)
APPLICATION SITE SCAB ( 1 FDA reports)
APPLICATION SITE SCAR ( 1 FDA reports)
ASTHENIA ( 1 FDA reports)
ATRIAL SEPTAL DEFECT ( 1 FDA reports)
BALANCE DISORDER ( 1 FDA reports)
BLOOD CREATININE INCREASED ( 1 FDA reports)
BLOOD TRIGLYCERIDES INCREASED ( 1 FDA reports)
BREAST DISORDER ( 1 FDA reports)
BURNING SENSATION ( 1 FDA reports)
CEREBRAL CALCIFICATION ( 1 FDA reports)
CONDITION AGGRAVATED ( 1 FDA reports)
DEEP VEIN THROMBOSIS ( 1 FDA reports)
DRUG DISPENSING ERROR ( 1 FDA reports)
DYSKINESIA ( 1 FDA reports)
DYSTONIA ( 1 FDA reports)
EAR DISORDER ( 1 FDA reports)
EAR INFECTION ( 1 FDA reports)
ECONOMIC PROBLEM ( 1 FDA reports)
ELECTROENCEPHALOGRAM ABNORMAL ( 1 FDA reports)
EMOTIONAL DISORDER ( 1 FDA reports)
ERYTHEMA ( 1 FDA reports)
EXTRAPYRAMIDAL DISORDER ( 1 FDA reports)
FACIAL PAIN ( 1 FDA reports)
FULL BLOOD COUNT DECREASED ( 1 FDA reports)
GAIT DISTURBANCE ( 1 FDA reports)
HAEMOCHROMATOSIS ( 1 FDA reports)
HEADACHE ( 1 FDA reports)
HEART RATE DECREASED ( 1 FDA reports)
HYPOVENTILATION ( 1 FDA reports)
IRRITABILITY ( 1 FDA reports)
MAJOR DEPRESSION ( 1 FDA reports)
MATERNAL DRUGS AFFECTING FOETUS ( 1 FDA reports)
MEDICATION ERROR ( 1 FDA reports)
MIDDLE INSOMNIA ( 1 FDA reports)
MUSCLE TWITCHING ( 1 FDA reports)
NERVOUSNESS ( 1 FDA reports)
NUCLEAR MAGNETIC RESONANCE IMAGING BRAIN ABNORMAL ( 1 FDA reports)
PHOTOSENSITIVITY REACTION ( 1 FDA reports)
POLYMYALGIA RHEUMATICA ( 1 FDA reports)
RENAL SURGERY ( 1 FDA reports)
RESPIRATORY DISTRESS ( 1 FDA reports)
RESPIRATORY RATE INCREASED ( 1 FDA reports)
SKIN BURNING SENSATION ( 1 FDA reports)
SKIN DISCOLOURATION ( 1 FDA reports)
SLEEP DISORDER ( 1 FDA reports)
SOCIAL PHOBIA ( 1 FDA reports)
SOMNOLENCE ( 1 FDA reports)
SUDDEN DEATH ( 1 FDA reports)
TARDIVE DYSKINESIA ( 1 FDA reports)
THERAPEUTIC RESPONSE UNEXPECTED ( 1 FDA reports)
TOOTHACHE ( 1 FDA reports)
TRANSIENT ISCHAEMIC ATTACK ( 1 FDA reports)
TREMOR ( 1 FDA reports)
VENTRICULAR SEPTAL DEFECT ( 1 FDA reports)
VIRAL INFECTION ( 1 FDA reports)
VOMITING ( 1 FDA reports)

© 2014 MedsFacts, Inc
Privacy Policy
Terms of Use