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CONDITION AGGRAVATED ( 8 FDA reports)
DRUG INEFFECTIVE ( 8 FDA reports)
BLOOD CHOLESTEROL INCREASED ( 7 FDA reports)
DEPRESSION ( 7 FDA reports)
HYPERTENSION ( 7 FDA reports)
ARTHRITIS ( 6 FDA reports)
BLOOD PRESSURE INCREASED ( 6 FDA reports)
MYOCARDIAL INFARCTION ( 6 FDA reports)
ABDOMINAL PAIN ( 5 FDA reports)
ABDOMINAL PAIN UPPER ( 5 FDA reports)
ANXIETY ( 5 FDA reports)
ASTHENIA ( 5 FDA reports)
CONSTIPATION ( 5 FDA reports)
ERYTHEMA ( 5 FDA reports)
FEELING HOT ( 5 FDA reports)
INTERVERTEBRAL DISC PROTRUSION ( 5 FDA reports)
PAIN ( 5 FDA reports)
PALPITATIONS ( 5 FDA reports)
ULCER HAEMORRHAGE ( 5 FDA reports)
ABASIA ( 4 FDA reports)
ASTHMA ( 4 FDA reports)
DISEASE RECURRENCE ( 4 FDA reports)
DIZZINESS ( 4 FDA reports)
FALL ( 4 FDA reports)
FIBROMYALGIA ( 4 FDA reports)
FLUSHING ( 4 FDA reports)
HEADACHE ( 4 FDA reports)
HYPOAESTHESIA ( 4 FDA reports)
LOWER LIMB FRACTURE ( 4 FDA reports)
OSTEOARTHRITIS ( 4 FDA reports)
OSTEOPOROSIS ( 4 FDA reports)
TREATMENT NONCOMPLIANCE ( 4 FDA reports)
URINARY INCONTINENCE ( 4 FDA reports)
UTERINE CANCER ( 4 FDA reports)
ARTHRALGIA ( 3 FDA reports)
BACK PAIN ( 3 FDA reports)
BENIGN PROSTATIC HYPERPLASIA ( 3 FDA reports)
BODY HEIGHT DECREASED ( 3 FDA reports)
CARDIAC MURMUR ( 3 FDA reports)
CERVICAL VERTEBRAL FRACTURE ( 3 FDA reports)
CHEST PAIN ( 3 FDA reports)
CONVULSION ( 3 FDA reports)
COUGH ( 3 FDA reports)
CYSTITIS ( 3 FDA reports)
DRUG EFFECT DECREASED ( 3 FDA reports)
GASTROOESOPHAGEAL REFLUX DISEASE ( 3 FDA reports)
HEART RATE INCREASED ( 3 FDA reports)
INCORRECT DOSE ADMINISTERED ( 3 FDA reports)
MUSCLE SPASMS ( 3 FDA reports)
MYALGIA ( 3 FDA reports)
PRECANCEROUS CELLS PRESENT ( 3 FDA reports)
SPINAL CORD COMPRESSION ( 3 FDA reports)
TRANSIENT ISCHAEMIC ATTACK ( 3 FDA reports)
URINARY RETENTION ( 3 FDA reports)
AMAUROSIS FUGAX ( 2 FDA reports)
APPLICATION SITE REACTION ( 2 FDA reports)
BREAST CYST ( 2 FDA reports)
CARDIAC FLUTTER ( 2 FDA reports)
DIABETES MELLITUS INADEQUATE CONTROL ( 2 FDA reports)
DRUG INTERACTION ( 2 FDA reports)
DYSKINESIA ( 2 FDA reports)
EXCORIATION ( 2 FDA reports)
EXFOLIATIVE RASH ( 2 FDA reports)
FEELING ABNORMAL ( 2 FDA reports)
GANGRENE ( 2 FDA reports)
HAEMATOCHEZIA ( 2 FDA reports)
HOT FLUSH ( 2 FDA reports)
INFECTION ( 2 FDA reports)
INJECTION SITE ERYTHEMA ( 2 FDA reports)
JOINT SWELLING ( 2 FDA reports)
LEG AMPUTATION ( 2 FDA reports)
LOSS OF CONSCIOUSNESS ( 2 FDA reports)
METRORRHAGIA ( 2 FDA reports)
MITRAL VALVE PROLAPSE ( 2 FDA reports)
MONOPLEGIA ( 2 FDA reports)
MUSCLE CONTRACTIONS INVOLUNTARY ( 2 FDA reports)
MUSCLE FATIGUE ( 2 FDA reports)
MUSCULOSKELETAL STIFFNESS ( 2 FDA reports)
NASOPHARYNGITIS ( 2 FDA reports)
NAUSEA ( 2 FDA reports)
ORAL CANDIDIASIS ( 2 FDA reports)
PHARMACEUTICAL PRODUCT COMPLAINT ( 2 FDA reports)
POST PROCEDURAL COMPLICATION ( 2 FDA reports)
PRURITUS ( 2 FDA reports)
RECTAL HAEMORRHAGE ( 2 FDA reports)
RECTAL PROLAPSE ( 2 FDA reports)
RHEUMATOID ARTHRITIS ( 2 FDA reports)
SINUSITIS ( 2 FDA reports)
TIC ( 2 FDA reports)
TOOTH DISORDER ( 2 FDA reports)
TOURETTE'S DISORDER ( 2 FDA reports)
VISION BLURRED ( 2 FDA reports)
WEIGHT INCREASED ( 2 FDA reports)
WRONG TECHNIQUE IN DRUG USAGE PROCESS ( 2 FDA reports)
ABDOMINAL DISCOMFORT ( 1 FDA reports)
ABDOMINOPLASTY ( 1 FDA reports)
AFFECTIVE DISORDER ( 1 FDA reports)
ALOPECIA ( 1 FDA reports)
ANGER ( 1 FDA reports)
ANORECTAL DISORDER ( 1 FDA reports)
ANOREXIA ( 1 FDA reports)
ANURIA ( 1 FDA reports)
ATRIAL SEPTAL DEFECT ( 1 FDA reports)
ATRIOVENTRICULAR BLOCK ( 1 FDA reports)
ATRIOVENTRICULAR BLOCK THIRD DEGREE ( 1 FDA reports)
BACTERIURIA ( 1 FDA reports)
BARIUM SWALLOW ABNORMAL ( 1 FDA reports)
BIOPSY UTERUS ABNORMAL ( 1 FDA reports)
BLADDER DISORDER ( 1 FDA reports)
BLADDER TRABECULATION ( 1 FDA reports)
BLINDNESS TRANSIENT ( 1 FDA reports)
BLINDNESS UNILATERAL ( 1 FDA reports)
BLISTER ( 1 FDA reports)
BLOOD DISORDER ( 1 FDA reports)
BLOOD PRESSURE IMMEASURABLE ( 1 FDA reports)
BLOOD PRESSURE INADEQUATELY CONTROLLED ( 1 FDA reports)
BODY HEIGHT INCREASED ( 1 FDA reports)
BODY TEMPERATURE INCREASED ( 1 FDA reports)
BONE DISORDER ( 1 FDA reports)
BREAST CANCER ( 1 FDA reports)
BREAST CANCER FEMALE ( 1 FDA reports)
CARDIAC ARREST ( 1 FDA reports)
CARDIAC FAILURE ( 1 FDA reports)
CARDIAC STRESS TEST ABNORMAL ( 1 FDA reports)
CELLULITIS ( 1 FDA reports)
CHILLS ( 1 FDA reports)
COLITIS ISCHAEMIC ( 1 FDA reports)
COLONIC POLYP ( 1 FDA reports)
CYANOSIS ( 1 FDA reports)
DEAFNESS ( 1 FDA reports)
DENTAL CARIES ( 1 FDA reports)
DEPRESSED LEVEL OF CONSCIOUSNESS ( 1 FDA reports)
DIABETES MELLITUS ( 1 FDA reports)
DIFFICULTY IN WALKING ( 1 FDA reports)
DISTURBANCE IN ATTENTION ( 1 FDA reports)
DRUG DOSE OMISSION ( 1 FDA reports)
DRUG EXPOSURE DURING PREGNANCY ( 1 FDA reports)
DRY SKIN ( 1 FDA reports)
DYSGRAPHIA ( 1 FDA reports)
DYSPNOEA ( 1 FDA reports)
EAR OPERATION ( 1 FDA reports)
ECONOMIC PROBLEM ( 1 FDA reports)
ENDOMETRIOSIS ( 1 FDA reports)
ENDOSCOPY ABNORMAL ( 1 FDA reports)
ERECTILE DYSFUNCTION ( 1 FDA reports)
EYE MOVEMENT DISORDER ( 1 FDA reports)
FACIAL BONES FRACTURE ( 1 FDA reports)
FATIGUE ( 1 FDA reports)
FEMALE GENITAL OPERATION ( 1 FDA reports)
FISTULA ( 1 FDA reports)
FOOD ALLERGY ( 1 FDA reports)
GAIT DISTURBANCE ( 1 FDA reports)
GASTRIC DISORDER ( 1 FDA reports)
GASTROINTESTINAL DISORDER ( 1 FDA reports)
GINGIVAL DISORDER ( 1 FDA reports)
GLOSSODYNIA ( 1 FDA reports)
HAEMATOMA ( 1 FDA reports)
HAEMORRHAGE ( 1 FDA reports)
HYPERHIDROSIS ( 1 FDA reports)
HYPERSOMNIA ( 1 FDA reports)
INFLUENZA ( 1 FDA reports)
INITIAL INSOMNIA ( 1 FDA reports)
INJECTION SITE DISCOLOURATION ( 1 FDA reports)
INJECTION SITE INFECTION ( 1 FDA reports)
INJECTION SITE PAIN ( 1 FDA reports)
INJECTION SITE PRURITUS ( 1 FDA reports)
INJECTION SITE SWELLING ( 1 FDA reports)
INJECTION SITE WARMTH ( 1 FDA reports)
INSOMNIA ( 1 FDA reports)
INTERVERTEBRAL DISC DEGENERATION ( 1 FDA reports)
INTERVERTEBRAL DISC DISORDER ( 1 FDA reports)
LARGE INTESTINAL ULCER ( 1 FDA reports)
MEDICAL DEVICE COMPLICATION ( 1 FDA reports)
MEMORY IMPAIRMENT ( 1 FDA reports)
MITRAL VALVE INCOMPETENCE ( 1 FDA reports)
MOBILITY DECREASED ( 1 FDA reports)
MOOD ALTERED ( 1 FDA reports)
MULTIPLE ALLERGIES ( 1 FDA reports)
MULTIPLE SCLEROSIS ( 1 FDA reports)
MUSCLE STRAIN ( 1 FDA reports)
MUSCLE TWITCHING ( 1 FDA reports)
MYDRIASIS ( 1 FDA reports)
MYOPATHY ( 1 FDA reports)
MYOPATHY STEROID ( 1 FDA reports)
NASAL ULCER ( 1 FDA reports)
NEPHROLITHIASIS ( 1 FDA reports)
OBSTRUCTIVE UROPATHY ( 1 FDA reports)
ORAL PAIN ( 1 FDA reports)
OXYGEN SATURATION DECREASED ( 1 FDA reports)
PAIN IN EXTREMITY ( 1 FDA reports)
PANIC ATTACK ( 1 FDA reports)
PARALYSIS ( 1 FDA reports)
PARKINSON'S DISEASE ( 1 FDA reports)
PARTIAL SEIZURES ( 1 FDA reports)
PERIPHERAL NERVE DECOMPRESSION ( 1 FDA reports)
PHARYNGEAL OEDEMA ( 1 FDA reports)
POOR QUALITY DRUG ADMINISTERED ( 1 FDA reports)
PROSTATE CANCER ( 1 FDA reports)
PULMONARY EMBOLISM ( 1 FDA reports)
PULMONARY HYPERTENSION ( 1 FDA reports)
PULMONARY VALVE DISEASE ( 1 FDA reports)
PULPITIS DENTAL ( 1 FDA reports)
RASH ( 1 FDA reports)
RECURRENT CANCER ( 1 FDA reports)
RESPIRATORY DISORDER ( 1 FDA reports)
RHINORRHOEA ( 1 FDA reports)
RIGHT VENTRICULAR FAILURE ( 1 FDA reports)
SICK SINUS SYNDROME ( 1 FDA reports)
SINUS DISORDER ( 1 FDA reports)
SKIN DEPIGMENTATION ( 1 FDA reports)
SKIN DISORDER ( 1 FDA reports)
SKIN EXFOLIATION ( 1 FDA reports)
SLEEP TALKING ( 1 FDA reports)
SNEEZING ( 1 FDA reports)
SOMNOLENCE ( 1 FDA reports)
SPINAL CORD INJURY ( 1 FDA reports)
SPINAL CORD PARALYSIS ( 1 FDA reports)
SPINAL DISORDER ( 1 FDA reports)
SPINAL FRACTURE ( 1 FDA reports)
SPINAL OPERATION ( 1 FDA reports)
SURGERY ( 1 FDA reports)
SYNCOPE ( 1 FDA reports)
TENDERNESS ( 1 FDA reports)
TENDON DISORDER ( 1 FDA reports)
TENDONITIS ( 1 FDA reports)
THERAPEUTIC RESPONSE DECREASED ( 1 FDA reports)
THERAPEUTIC RESPONSE UNEXPECTED WITH DRUG SUBSTITUTION ( 1 FDA reports)
THORACIC VERTEBRAL FRACTURE ( 1 FDA reports)
TOOTH ABSCESS ( 1 FDA reports)
TOOTH EXTRACTION ( 1 FDA reports)
TOOTH INFECTION ( 1 FDA reports)
TREMOR ( 1 FDA reports)
TRIGEMINAL NEURALGIA ( 1 FDA reports)
URETHRAL OBSTRUCTION ( 1 FDA reports)
URETHRAL STENOSIS ( 1 FDA reports)
URINARY TRACT INFECTION ( 1 FDA reports)
URTICARIA ( 1 FDA reports)
UTERINE DISORDER ( 1 FDA reports)
UTERINE SPASM ( 1 FDA reports)
VAGINAL DISCHARGE ( 1 FDA reports)
VENTRICULAR ASYSTOLE ( 1 FDA reports)
VENTRICULAR TACHYCARDIA ( 1 FDA reports)
VISUAL ACUITY REDUCED ( 1 FDA reports)
WHITE BLOOD CELL COUNT INCREASED ( 1 FDA reports)
WOUND HAEMORRHAGE ( 1 FDA reports)
YAWNING ( 1 FDA reports)

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