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

ARTHRALGIA ( 18 FDA reports)
PAIN ( 18 FDA reports)
ANXIETY ( 17 FDA reports)
FATIGUE ( 13 FDA reports)
DEPRESSION ( 12 FDA reports)
HEADACHE ( 12 FDA reports)
CHOLELITHIASIS ( 11 FDA reports)
INJURY ( 11 FDA reports)
ASTHENIA ( 10 FDA reports)
CONSTIPATION ( 10 FDA reports)
COUGH ( 10 FDA reports)
HAEMORRHOIDS ( 10 FDA reports)
FALL ( 9 FDA reports)
GAIT DISTURBANCE ( 9 FDA reports)
NAUSEA ( 9 FDA reports)
ANAEMIA ( 8 FDA reports)
DIARRHOEA ( 8 FDA reports)
EMOTIONAL DISTRESS ( 8 FDA reports)
HYPERTENSION ( 8 FDA reports)
INSOMNIA ( 8 FDA reports)
OSTEOARTHRITIS ( 8 FDA reports)
PAIN IN JAW ( 8 FDA reports)
PYREXIA ( 8 FDA reports)
BACK PAIN ( 7 FDA reports)
BONE PAIN ( 7 FDA reports)
BRONCHITIS ( 7 FDA reports)
CHEST PAIN ( 7 FDA reports)
COMPRESSION FRACTURE ( 7 FDA reports)
DIZZINESS ( 7 FDA reports)
GASTROOESOPHAGEAL REFLUX DISEASE ( 7 FDA reports)
MUSCLE SPASMS ( 7 FDA reports)
OSTEOPOROSIS ( 7 FDA reports)
SLEEP DISORDER ( 7 FDA reports)
SPINAL OSTEOARTHRITIS ( 7 FDA reports)
SYNCOPE ( 7 FDA reports)
VISION BLURRED ( 7 FDA reports)
WEIGHT DECREASED ( 7 FDA reports)
ABDOMINAL PAIN ( 6 FDA reports)
COMPUTERISED TOMOGRAM ABNORMAL ( 6 FDA reports)
DYSPNOEA EXERTIONAL ( 6 FDA reports)
HYPOAESTHESIA ( 6 FDA reports)
PAIN IN EXTREMITY ( 6 FDA reports)
BONE DISORDER ( 5 FDA reports)
CROHN'S DISEASE ( 5 FDA reports)
DECREASED APPETITE ( 5 FDA reports)
GALLBLADDER DISORDER ( 5 FDA reports)
MUSCULAR WEAKNESS ( 5 FDA reports)
NEUROPATHY PERIPHERAL ( 5 FDA reports)
OSTEONECROSIS ( 5 FDA reports)
OSTEOPENIA ( 5 FDA reports)
PARAESTHESIA ( 5 FDA reports)
SINUSITIS ( 5 FDA reports)
WEIGHT INCREASED ( 5 FDA reports)
ABDOMINAL PAIN UPPER ( 4 FDA reports)
BILIARY COLIC ( 4 FDA reports)
BLOOD CREATININE INCREASED ( 4 FDA reports)
BONE SCAN ABNORMAL ( 4 FDA reports)
CERVICAL SPINAL STENOSIS ( 4 FDA reports)
COLITIS ULCERATIVE ( 4 FDA reports)
CONFUSIONAL STATE ( 4 FDA reports)
DENTAL CARIES ( 4 FDA reports)
DISABILITY ( 4 FDA reports)
DISEASE PROGRESSION ( 4 FDA reports)
FEBRILE NEUTROPENIA ( 4 FDA reports)
FOOT FRACTURE ( 4 FDA reports)
GASTROENTERITIS VIRAL ( 4 FDA reports)
GENERAL PHYSICAL HEALTH DETERIORATION ( 4 FDA reports)
GINGIVAL ATROPHY ( 4 FDA reports)
GINGIVAL ULCERATION ( 4 FDA reports)
GLOMERULAR FILTRATION RATE DECREASED ( 4 FDA reports)
HAEMATOCHEZIA ( 4 FDA reports)
HAEMOPTYSIS ( 4 FDA reports)
HIATUS HERNIA ( 4 FDA reports)
HYPERLIPIDAEMIA ( 4 FDA reports)
HYPERREFLEXIA ( 4 FDA reports)
HYPONATRAEMIA ( 4 FDA reports)
IMPAIRED HEALING ( 4 FDA reports)
INFLAMMATORY BOWEL DISEASE ( 4 FDA reports)
INTERVERTEBRAL DISC PROTRUSION ( 4 FDA reports)
KYPHOSIS ( 4 FDA reports)
LHERMITTE'S SIGN ( 4 FDA reports)
LIGAMENT INJURY ( 4 FDA reports)
LIMB INJURY ( 4 FDA reports)
LUNG DISORDER ( 4 FDA reports)
LUNG HYPERINFLATION ( 4 FDA reports)
LUNG NEOPLASM ( 4 FDA reports)
NEPHROSCLEROSIS ( 4 FDA reports)
NUCLEAR MAGNETIC RESONANCE IMAGING ABNORMAL ( 4 FDA reports)
OEDEMA PERIPHERAL ( 4 FDA reports)
ONYCHOMYCOSIS ( 4 FDA reports)
ORAL DISORDER ( 4 FDA reports)
ORAL INFECTION ( 4 FDA reports)
ORAL MUCOSAL EXFOLIATION ( 4 FDA reports)
PERIRECTAL ABSCESS ( 4 FDA reports)
PULMONARY EMBOLISM ( 4 FDA reports)
RASH ( 4 FDA reports)
RENAL FAILURE CHRONIC ( 4 FDA reports)
SCAR ( 4 FDA reports)
SLEEP APNOEA SYNDROME ( 4 FDA reports)
SPINAL X-RAY ABNORMAL ( 4 FDA reports)
SPUTUM DISCOLOURED ( 4 FDA reports)
TANDEM GAIT TEST ABNORMAL ( 4 FDA reports)
THROMBOCYTOPENIA ( 4 FDA reports)
TONGUE ULCERATION ( 4 FDA reports)
TOOTH DISORDER ( 4 FDA reports)
TOTAL LUNG CAPACITY DECREASED ( 4 FDA reports)
TREMOR ( 4 FDA reports)
UPPER RESPIRATORY TRACT INFECTION ( 4 FDA reports)
VERTEBRAL COLUMN MASS ( 4 FDA reports)
WEIGHT FLUCTUATION ( 4 FDA reports)
ABDOMINAL DISTENSION ( 3 FDA reports)
ACUTE SINUSITIS ( 3 FDA reports)
AFFECTIVE DISORDER ( 3 FDA reports)
ARTHRITIS ( 3 FDA reports)
ASTHMA ( 3 FDA reports)
BLADDER CYST ( 3 FDA reports)
BLOOD PRESSURE INCREASED ( 3 FDA reports)
CARDIOMEGALY ( 3 FDA reports)
CELLULITIS STAPHYLOCOCCAL ( 3 FDA reports)
CEREBRAL ATROPHY ( 3 FDA reports)
CYSTITIS ( 3 FDA reports)
CYSTOCELE ( 3 FDA reports)
DECUBITUS ULCER ( 3 FDA reports)
DEHYDRATION ( 3 FDA reports)
DYSPHAGIA ( 3 FDA reports)
DYSPNOEA ( 3 FDA reports)
EAR CONGESTION ( 3 FDA reports)
EXPOSED BONE IN JAW ( 3 FDA reports)
FACET JOINT SYNDROME ( 3 FDA reports)
FUNGAL INFECTION ( 3 FDA reports)
GINGIVAL PAIN ( 3 FDA reports)
HOT FLUSH ( 3 FDA reports)
HYPERAESTHESIA ( 3 FDA reports)
HYPOACUSIS ( 3 FDA reports)
INCONTINENCE ( 3 FDA reports)
INCREASED TENDENCY TO BRUISE ( 3 FDA reports)
INFLUENZA ( 3 FDA reports)
INTERVERTEBRAL DISC DEGENERATION ( 3 FDA reports)
LEUKOPENIA ( 3 FDA reports)
LUMBAR SPINAL STENOSIS ( 3 FDA reports)
MALAISE ( 3 FDA reports)
MASTICATION DISORDER ( 3 FDA reports)
MEMORY IMPAIRMENT ( 3 FDA reports)
MONOCLONAL IMMUNOGLOBULIN PRESENT ( 3 FDA reports)
MULTIPLE MYELOMA ( 3 FDA reports)
MUSCULOSKELETAL DISCOMFORT ( 3 FDA reports)
MYALGIA ( 3 FDA reports)
MYELODYSPLASTIC SYNDROME ( 3 FDA reports)
NEOPLASM MALIGNANT ( 3 FDA reports)
NERVOUSNESS ( 3 FDA reports)
NIGHT SWEATS ( 3 FDA reports)
OBESITY ( 3 FDA reports)
OEDEMA ( 3 FDA reports)
ORAL PAIN ( 3 FDA reports)
OSTEITIS ( 3 FDA reports)
OSTEONECROSIS OF JAW ( 3 FDA reports)
OSTEOSCLEROSIS ( 3 FDA reports)
PHARYNGITIS ( 3 FDA reports)
PLEURITIC PAIN ( 3 FDA reports)
PROCTITIS ( 3 FDA reports)
PROTEIN TOTAL INCREASED ( 3 FDA reports)
PSYCHOMOTOR HYPERACTIVITY ( 3 FDA reports)
PULMONARY INFARCTION ( 3 FDA reports)
RECTOCELE ( 3 FDA reports)
RENAL CYST ( 3 FDA reports)
STOMATITIS ( 3 FDA reports)
STRESS ( 3 FDA reports)
TEMPOROMANDIBULAR JOINT SYNDROME ( 3 FDA reports)
THROMBOSIS IN DEVICE ( 3 FDA reports)
TOOTHACHE ( 3 FDA reports)
ULCER ( 3 FDA reports)
VAGINAL DISCHARGE ( 3 FDA reports)
VAGINAL INFECTION ( 3 FDA reports)
VENOUS THROMBOSIS LIMB ( 3 FDA reports)
ADRENAL INSUFFICIENCY ( 2 FDA reports)
ANGINA PECTORIS ( 2 FDA reports)
AORTIC ANEURYSM ( 2 FDA reports)
AORTIC ANEURYSM REPAIR ( 2 FDA reports)
AORTIC VALVE REPLACEMENT ( 2 FDA reports)
ARTERIOGRAM CORONARY ( 2 FDA reports)
ARTERIOSCLEROSIS ( 2 FDA reports)
BILIARY DYSKINESIA ( 2 FDA reports)
BLISTER ( 2 FDA reports)
BLOOD GLUCOSE INCREASED ( 2 FDA reports)
BLOOD THYROID STIMULATING HORMONE DECREASED ( 2 FDA reports)
BREAST CANCER ( 2 FDA reports)
BREAST CYST ( 2 FDA reports)
CARDIAC ENZYMES INCREASED ( 2 FDA reports)
CARDIAC SEPTAL DEFECT ( 2 FDA reports)
CARDIAC STRESS TEST ( 2 FDA reports)
CATHETERISATION CARDIAC ABNORMAL ( 2 FDA reports)
CHOLECYSTITIS ( 2 FDA reports)
CHOLECYSTITIS CHRONIC ( 2 FDA reports)
CORONARY ARTERY BYPASS ( 2 FDA reports)
DEAFNESS ( 2 FDA reports)
DEEP VEIN THROMBOSIS ( 2 FDA reports)
DIVERTICULITIS ( 2 FDA reports)
DRUG LEVEL INCREASED ( 2 FDA reports)
DYSTONIA ( 2 FDA reports)
EAR PAIN ( 2 FDA reports)
EJECTION FRACTION DECREASED ( 2 FDA reports)
EPISTAXIS ( 2 FDA reports)
FIBROMYALGIA ( 2 FDA reports)
FOOT OPERATION ( 2 FDA reports)
GLAUCOMA ( 2 FDA reports)
GOUT ( 2 FDA reports)
HIGH DENSITY LIPOPROTEIN DECREASED ( 2 FDA reports)
JOINT SWELLING ( 2 FDA reports)
KNEE ARTHROPLASTY ( 2 FDA reports)
LOW DENSITY LIPOPROTEIN INCREASED ( 2 FDA reports)
MAMMOGRAM ( 2 FDA reports)
MASTECTOMY ( 2 FDA reports)
MOOD SWINGS ( 2 FDA reports)
MUSCLE TIGHTNESS ( 2 FDA reports)
MYOCARDIAL INFARCTION ( 2 FDA reports)
NEPHROLITHIASIS ( 2 FDA reports)
NERVE INJURY ( 2 FDA reports)
OESOPHAGOSCOPY ABNORMAL ( 2 FDA reports)
OESTROGEN RECEPTOR ASSAY POSITIVE ( 2 FDA reports)
ORGAN FAILURE ( 2 FDA reports)
PENILE PAIN ( 2 FDA reports)
POLLAKIURIA ( 2 FDA reports)
PROGESTERONE RECEPTOR ASSAY POSITIVE ( 2 FDA reports)
PRURITUS ( 2 FDA reports)
SCAN MYOCARDIAL PERFUSION ( 2 FDA reports)
SENSATION OF HEAVINESS ( 2 FDA reports)
SKIN HAEMORRHAGE ( 2 FDA reports)
SKIN PAPILLOMA ( 2 FDA reports)
THERAPEUTIC RESPONSE DECREASED ( 2 FDA reports)
THROMBOSIS ( 2 FDA reports)
TRI-IODOTHYRONINE INCREASED ( 2 FDA reports)
URINARY TRACT INFECTION ( 2 FDA reports)
VISUAL ACUITY REDUCED ( 2 FDA reports)
VOMITING ( 2 FDA reports)
ABDOMINAL ADHESIONS ( 1 FDA reports)
ABDOMINAL HERNIA ( 1 FDA reports)
ACCIDENTAL OVERDOSE ( 1 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 1 FDA reports)
ANEURYSM ( 1 FDA reports)
ANORECTAL STENOSIS ( 1 FDA reports)
ANOREXIA ( 1 FDA reports)
ANXIETY DISORDER ( 1 FDA reports)
APHTHOUS STOMATITIS ( 1 FDA reports)
AREFLEXIA ( 1 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 1 FDA reports)
ASTIGMATISM ( 1 FDA reports)
ATELECTASIS ( 1 FDA reports)
AZOTAEMIA ( 1 FDA reports)
BACK INJURY ( 1 FDA reports)
BALANCE DISORDER ( 1 FDA reports)
BARRETT'S OESOPHAGUS ( 1 FDA reports)
BEDRIDDEN ( 1 FDA reports)
BILE DUCT STONE ( 1 FDA reports)
BLOOD CHOLESTEROL INCREASED ( 1 FDA reports)
BLOOD GLUCOSE DECREASED ( 1 FDA reports)
BLOOD PRESSURE DECREASED ( 1 FDA reports)
BONE LESION ( 1 FDA reports)
BRAIN NEOPLASM ( 1 FDA reports)
BRAIN STEM STROKE ( 1 FDA reports)
CARDIAC FAILURE CONGESTIVE ( 1 FDA reports)
CELLULITIS ( 1 FDA reports)
CENTRAL VENOUS CATHETER REMOVAL ( 1 FDA reports)
CERVICAL MYELOPATHY ( 1 FDA reports)
CHOLECYSTECTOMY ( 1 FDA reports)
CHOLECYSTITIS ACUTE ( 1 FDA reports)
COLONIC STENOSIS ( 1 FDA reports)
COMPLETED SUICIDE ( 1 FDA reports)
CONDITION AGGRAVATED ( 1 FDA reports)
CONTUSION ( 1 FDA reports)
CONVULSION ( 1 FDA reports)
DEATH ( 1 FDA reports)
DEFAECATION URGENCY ( 1 FDA reports)
DEFORMITY ( 1 FDA reports)
DEPENDENCE ( 1 FDA reports)
DIABETIC ULCER ( 1 FDA reports)
DIASTOLIC DYSFUNCTION ( 1 FDA reports)
DISORIENTATION ( 1 FDA reports)
DRUG ABUSE ( 1 FDA reports)
DRUG INEFFECTIVE ( 1 FDA reports)
DRUG WITHDRAWAL SYNDROME ( 1 FDA reports)
DYSSTASIA ( 1 FDA reports)
ENDOCRINE DISORDER ( 1 FDA reports)
ENTERITIS ( 1 FDA reports)
ERYTHEMA ( 1 FDA reports)
EYE PRURITUS ( 1 FDA reports)
FAECAL INCONTINENCE ( 1 FDA reports)
FAECES DISCOLOURED ( 1 FDA reports)
FIBROSIS ( 1 FDA reports)
FLATULENCE ( 1 FDA reports)
FLUID RETENTION ( 1 FDA reports)
FLUSHING ( 1 FDA reports)
FUNGAL SKIN INFECTION ( 1 FDA reports)
GALLBLADDER INJURY ( 1 FDA reports)
GASTROINTESTINAL DISORDER ( 1 FDA reports)
GASTROINTESTINAL HAEMORRHAGE ( 1 FDA reports)
GASTROINTESTINAL INFLAMMATION ( 1 FDA reports)
GASTROINTESTINAL OEDEMA ( 1 FDA reports)
GINGIVITIS ( 1 FDA reports)
GRIP STRENGTH DECREASED ( 1 FDA reports)
HAEMORRHOIDAL HAEMORRHAGE ( 1 FDA reports)
HEART RATE INCREASED ( 1 FDA reports)
HEPATITIS C ( 1 FDA reports)
HYPERADRENALISM ( 1 FDA reports)
HYPOCALCAEMIA ( 1 FDA reports)
HYPOMAGNESAEMIA ( 1 FDA reports)
HYPOPHAGIA ( 1 FDA reports)
IMMUNOSUPPRESSION ( 1 FDA reports)
INCORRECT DOSE ADMINISTERED ( 1 FDA reports)
INFECTION ( 1 FDA reports)
INJECTION SITE IRRITATION ( 1 FDA reports)
INJECTION SITE REACTION ( 1 FDA reports)
INTERNATIONAL NORMALISED RATIO INCREASED ( 1 FDA reports)
INTERVERTEBRAL DISC DISORDER ( 1 FDA reports)
INTESTINAL DILATATION ( 1 FDA reports)
INTESTINAL MUCOSAL HYPERTROPHY ( 1 FDA reports)
INTESTINAL OBSTRUCTION ( 1 FDA reports)
INTESTINAL STENOSIS ( 1 FDA reports)
INTESTINAL ULCER ( 1 FDA reports)
INTRA-CEREBRAL ANEURYSM OPERATION ( 1 FDA reports)
INTRAOCULAR LENS IMPLANT ( 1 FDA reports)
INTRAOCULAR PRESSURE INCREASED ( 1 FDA reports)
INTUSSUSCEPTION ( 1 FDA reports)
LETHARGY ( 1 FDA reports)
MALABSORPTION ( 1 FDA reports)
MALIGNANT NEOPLASM PROGRESSION ( 1 FDA reports)
MALNUTRITION ( 1 FDA reports)
MENTAL DISORDER ( 1 FDA reports)
MOVEMENT DISORDER ( 1 FDA reports)
MUSCLE ATROPHY ( 1 FDA reports)
MUSCULOSKELETAL PAIN ( 1 FDA reports)
MYELOPROLIFERATIVE DISORDER ( 1 FDA reports)
MYOPIA ( 1 FDA reports)
NAIL DISORDER ( 1 FDA reports)
NASAL DISCOMFORT ( 1 FDA reports)
NECK PAIN ( 1 FDA reports)
NEUTROPENIA ( 1 FDA reports)
NOCTURIA ( 1 FDA reports)
OPTIC DISC DISORDER ( 1 FDA reports)
OPTIC NERVE DISORDER ( 1 FDA reports)
ORAL HERPES ( 1 FDA reports)
OROPHARYNGEAL PAIN ( 1 FDA reports)
OVERDOSE ( 1 FDA reports)
PANIC ATTACK ( 1 FDA reports)
PANIC REACTION ( 1 FDA reports)
PEAU D'ORANGE ( 1 FDA reports)
PHARYNGEAL DISORDER ( 1 FDA reports)
PHARYNGEAL ERYTHEMA ( 1 FDA reports)
PNEUMONIA ( 1 FDA reports)
POLYARTHRITIS ( 1 FDA reports)
POLYNEUROPATHY ( 1 FDA reports)
POST PROCEDURAL COMPLICATION ( 1 FDA reports)
PRODUCT QUALITY ISSUE ( 1 FDA reports)
PULMONARY CALCIFICATION ( 1 FDA reports)
RADIUS FRACTURE ( 1 FDA reports)
RECTAL HAEMORRHAGE ( 1 FDA reports)
RENAL FAILURE ( 1 FDA reports)
RESPIRATORY ARREST ( 1 FDA reports)
RESPIRATORY DISORDER ( 1 FDA reports)
RESPIRATORY DISTRESS ( 1 FDA reports)
RETINAL PIGMENTATION ( 1 FDA reports)
RETINOPATHY HAEMORRHAGIC ( 1 FDA reports)
RHINORRHOEA ( 1 FDA reports)
SENSORY DISTURBANCE ( 1 FDA reports)
SKULL FRACTURE ( 1 FDA reports)
SMALL INTESTINAL BACTERIAL OVERGROWTH ( 1 FDA reports)
SMALL INTESTINAL OBSTRUCTION ( 1 FDA reports)
SMALL INTESTINAL STENOSIS ( 1 FDA reports)
SOMNOLENCE ( 1 FDA reports)
SPINAL FRACTURE ( 1 FDA reports)
SPINAL FUSION SURGERY ( 1 FDA reports)
SPINAL LAMINECTOMY ( 1 FDA reports)
SUBCUTANEOUS ABSCESS ( 1 FDA reports)
SUDDEN VISUAL LOSS ( 1 FDA reports)
SWELLING ( 1 FDA reports)
TARDIVE DYSKINESIA ( 1 FDA reports)
TENDON RUPTURE ( 1 FDA reports)
TINNITUS ( 1 FDA reports)
TOOTH EXTRACTION ( 1 FDA reports)
TOOTH LOSS ( 1 FDA reports)
TYPE 2 DIABETES MELLITUS ( 1 FDA reports)
ULNA FRACTURE ( 1 FDA reports)
VERTIGO ( 1 FDA reports)
VICTIM OF ELDER ABUSE ( 1 FDA reports)
VIRAL INFECTION ( 1 FDA reports)
VISCERAL CONGESTION ( 1 FDA reports)
VISUAL IMPAIRMENT ( 1 FDA reports)

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