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

FATIGUE ( 91 FDA reports)
ANAEMIA ( 77 FDA reports)
OSTEONECROSIS OF JAW ( 66 FDA reports)
DIARRHOEA ( 65 FDA reports)
NAUSEA ( 64 FDA reports)
ANXIETY ( 63 FDA reports)
DIZZINESS ( 63 FDA reports)
DYSPNOEA ( 61 FDA reports)
PAIN ( 60 FDA reports)
HEADACHE ( 59 FDA reports)
CHEST PAIN ( 57 FDA reports)
DEPRESSION ( 56 FDA reports)
CONSTIPATION ( 54 FDA reports)
ARTHRALGIA ( 50 FDA reports)
ASTHENIA ( 46 FDA reports)
BRONCHITIS ( 45 FDA reports)
GASTROOESOPHAGEAL REFLUX DISEASE ( 45 FDA reports)
HYPOACUSIS ( 45 FDA reports)
OSTEOPOROSIS ( 45 FDA reports)
ABDOMINAL PAIN ( 43 FDA reports)
BACK PAIN ( 43 FDA reports)
HYPOAESTHESIA ( 42 FDA reports)
LOOSE TOOTH ( 42 FDA reports)
MUSCLE SPASMS ( 42 FDA reports)
WOUND DEHISCENCE ( 42 FDA reports)
BONE DISORDER ( 39 FDA reports)
BONE PAIN ( 38 FDA reports)
PARAESTHESIA ( 38 FDA reports)
VISUAL ACUITY REDUCED ( 38 FDA reports)
VOMITING ( 38 FDA reports)
BLOOD GLUCOSE INCREASED ( 37 FDA reports)
COUGH ( 37 FDA reports)
MULTIPLE MYELOMA ( 37 FDA reports)
FALL ( 36 FDA reports)
GINGIVAL ULCERATION ( 36 FDA reports)
INJURY ( 36 FDA reports)
PNEUMONIA ( 36 FDA reports)
RIB FRACTURE ( 35 FDA reports)
THROMBOCYTOPENIA ( 35 FDA reports)
MYALGIA ( 34 FDA reports)
TREMOR ( 34 FDA reports)
GAIT DISTURBANCE ( 33 FDA reports)
SPINAL OSTEOARTHRITIS ( 33 FDA reports)
TOOTH INFECTION ( 33 FDA reports)
DYSGEUSIA ( 32 FDA reports)
DYSPHAGIA ( 32 FDA reports)
HYPOTHYROIDISM ( 32 FDA reports)
SWELLING ( 32 FDA reports)
CATARACT ( 31 FDA reports)
DEEP VEIN THROMBOSIS ( 31 FDA reports)
DRY EYE ( 31 FDA reports)
HAEMORRHOIDS ( 31 FDA reports)
MITRAL VALVE INCOMPETENCE ( 31 FDA reports)
NEUROPATHY PERIPHERAL ( 31 FDA reports)
SYNCOPE ( 31 FDA reports)
AMNESIA ( 30 FDA reports)
CARDIAC MURMUR ( 30 FDA reports)
ORAL PAIN ( 30 FDA reports)
WEIGHT DECREASED ( 30 FDA reports)
AORTIC STENOSIS ( 29 FDA reports)
MENTAL STATUS CHANGES ( 29 FDA reports)
VENTRICULAR HYPERTROPHY ( 29 FDA reports)
CARDIAC FAILURE CONGESTIVE ( 28 FDA reports)
GENERAL PHYSICAL HEALTH DETERIORATION ( 28 FDA reports)
OSTEOPENIA ( 28 FDA reports)
ATELECTASIS ( 27 FDA reports)
ERYTHEMA ( 27 FDA reports)
INSOMNIA ( 27 FDA reports)
MUSCULOSKELETAL STIFFNESS ( 27 FDA reports)
NEPHROLITHIASIS ( 27 FDA reports)
SINUS CONGESTION ( 27 FDA reports)
BLOOD PRESSURE INCREASED ( 26 FDA reports)
ERECTILE DYSFUNCTION ( 26 FDA reports)
HYPERHIDROSIS ( 26 FDA reports)
NERVOUSNESS ( 26 FDA reports)
URTICARIA ( 26 FDA reports)
VERTIGO ( 26 FDA reports)
GINGIVAL PAIN ( 25 FDA reports)
INTERVERTEBRAL DISC PROTRUSION ( 25 FDA reports)
SOMNOLENCE ( 25 FDA reports)
TINNITUS ( 25 FDA reports)
TOOTHACHE ( 25 FDA reports)
ASTHMA ( 24 FDA reports)
CHOLELITHIASIS ( 24 FDA reports)
EXOSTOSIS ( 24 FDA reports)
GINGIVAL RECESSION ( 24 FDA reports)
HYPOGONADISM ( 24 FDA reports)
HYPONATRAEMIA ( 24 FDA reports)
PLATELET COUNT DECREASED ( 24 FDA reports)
RENAL IMPAIRMENT ( 24 FDA reports)
SQUAMOUS CELL CARCINOMA OF SKIN ( 24 FDA reports)
DRY SKIN ( 23 FDA reports)
HAEMOGLOBIN DECREASED ( 23 FDA reports)
HALLUCINATION ( 23 FDA reports)
AORTIC VALVE INCOMPETENCE ( 22 FDA reports)
ATRIAL TACHYCARDIA ( 22 FDA reports)
ATRIOVENTRICULAR BLOCK COMPLETE ( 22 FDA reports)
BARRETT'S OESOPHAGUS ( 22 FDA reports)
BRADYCARDIA ( 22 FDA reports)
CHRONIC OBSTRUCTIVE PULMONARY DISEASE ( 22 FDA reports)
DENTAL CARIES ( 22 FDA reports)
DISTURBANCE IN ATTENTION ( 22 FDA reports)
DIVERTICULITIS ( 22 FDA reports)
DYSURIA ( 22 FDA reports)
HYPERCHOLESTEROLAEMIA ( 22 FDA reports)
HYPERSENSITIVITY ( 22 FDA reports)
SEBORRHOEIC DERMATITIS ( 22 FDA reports)
SOFT TISSUE INFLAMMATION ( 22 FDA reports)
THROMBOTIC THROMBOCYTOPENIC PURPURA ( 22 FDA reports)
UMBILICAL HERNIA ( 22 FDA reports)
X-RAY ABNORMAL ( 22 FDA reports)
AORTIC ARTERIOSCLEROSIS ( 21 FDA reports)
COGNITIVE DISORDER ( 21 FDA reports)
EYE PAIN ( 21 FDA reports)
GASTRITIS ( 21 FDA reports)
HAEMATOCRIT ABNORMAL ( 21 FDA reports)
HALLUCINATION, VISUAL ( 21 FDA reports)
JAW DISORDER ( 21 FDA reports)
PULMONARY HYPERTENSION ( 21 FDA reports)
RASH PRURITIC ( 21 FDA reports)
RETINAL DETACHMENT ( 21 FDA reports)
VISION BLURRED ( 21 FDA reports)
VITREOUS FLOATERS ( 21 FDA reports)
ACQUIRED OESOPHAGEAL WEB ( 20 FDA reports)
ARTERIOSCLEROSIS ( 20 FDA reports)
AUTONOMIC NEUROPATHY ( 20 FDA reports)
BONE DENSITY DECREASED ( 20 FDA reports)
BREAST HYPERPLASIA ( 20 FDA reports)
CARDIOMYOPATHY ( 20 FDA reports)
CAROTID ARTERY STENOSIS ( 20 FDA reports)
DEHYDRATION ( 20 FDA reports)
DEMENTIA WITH LEWY BODIES ( 20 FDA reports)
DERMATOPHYTOSIS ( 20 FDA reports)
GYNAECOMASTIA ( 20 FDA reports)
HEARING DISABILITY ( 20 FDA reports)
HERNIA ( 20 FDA reports)
INFECTION ( 20 FDA reports)
IRRITABILITY ( 20 FDA reports)
LACUNAR INFARCTION ( 20 FDA reports)
METASTASES TO SPINE ( 20 FDA reports)
MUSCLE STRAIN ( 20 FDA reports)
OLFACTORY NERVE DISORDER ( 20 FDA reports)
OSTEOSCLEROSIS ( 20 FDA reports)
PARKINSON'S DISEASE ( 20 FDA reports)
POOR DENTAL CONDITION ( 20 FDA reports)
RENAL FAILURE ( 20 FDA reports)
TEMPORAL ARTERITIS ( 20 FDA reports)
TOURETTE'S DISORDER ( 20 FDA reports)
WOUND INFECTION ( 20 FDA reports)
HYPERTENSION ( 19 FDA reports)
HYPOKALAEMIA ( 19 FDA reports)
INTERVERTEBRAL DISC DEGENERATION ( 19 FDA reports)
NOCTURIA ( 19 FDA reports)
PANCYTOPENIA ( 19 FDA reports)
PLEURAL EFFUSION ( 19 FDA reports)
PRESYNCOPE ( 19 FDA reports)
PYREXIA ( 19 FDA reports)
SPINAL COMPRESSION FRACTURE ( 19 FDA reports)
TENDON INJURY ( 19 FDA reports)
OEDEMA PERIPHERAL ( 18 FDA reports)
BLEPHARITIS ( 17 FDA reports)
CELLULITIS ( 17 FDA reports)
DRUG INEFFECTIVE ( 17 FDA reports)
FLUSHING ( 17 FDA reports)
HYPOMAGNESAEMIA ( 17 FDA reports)
INAPPROPRIATE ANTIDIURETIC HORMONE SECRETION ( 17 FDA reports)
NODULE ( 17 FDA reports)
ORTHOSTATIC HYPOTENSION ( 17 FDA reports)
OSTEOARTHRITIS ( 17 FDA reports)
SINUSITIS ( 17 FDA reports)
ANXIETY DISORDER ( 16 FDA reports)
CHOROIDAL DETACHMENT ( 16 FDA reports)
COMPRESSION FRACTURE ( 16 FDA reports)
DECREASED APPETITE ( 16 FDA reports)
EMOTIONAL DISTRESS ( 16 FDA reports)
HIATUS HERNIA ( 16 FDA reports)
MACULAR HOLE ( 16 FDA reports)
ABDOMINAL PAIN UPPER ( 15 FDA reports)
ACTINIC ELASTOSIS ( 15 FDA reports)
ACTINIC KERATOSIS ( 15 FDA reports)
CORONARY ARTERY DISEASE ( 15 FDA reports)
DISCOMFORT ( 15 FDA reports)
FEELING ABNORMAL ( 15 FDA reports)
HYPOPHAGIA ( 15 FDA reports)
HYPOVOLAEMIA ( 15 FDA reports)
INCREASED APPETITE ( 15 FDA reports)
SINUS BRADYCARDIA ( 15 FDA reports)
SPINAL COLUMN STENOSIS ( 15 FDA reports)
STEM CELL TRANSPLANT ( 15 FDA reports)
VITAMIN B12 DEFICIENCY ( 15 FDA reports)
BASAL CELL CARCINOMA ( 14 FDA reports)
CARDIOMEGALY ( 14 FDA reports)
DIVERTICULUM ( 14 FDA reports)
EYE SWELLING ( 14 FDA reports)
JOINT INJURY ( 14 FDA reports)
OCULAR HYPERAEMIA ( 14 FDA reports)
OSTEOMYELITIS ( 14 FDA reports)
SKIN INFECTION ( 14 FDA reports)
SPONDYLOLISTHESIS ( 14 FDA reports)
WEIGHT INCREASED ( 14 FDA reports)
ABDOMINAL HERNIA ( 13 FDA reports)
ACROCHORDON ( 13 FDA reports)
AFFECTIVE DISORDER ( 13 FDA reports)
CERVICAL DYSPLASIA ( 13 FDA reports)
DECREASED INTEREST ( 13 FDA reports)
DEFORMITY ( 13 FDA reports)
DERMAL CYST ( 13 FDA reports)
DIABETES MELLITUS ( 13 FDA reports)
DRY MOUTH ( 13 FDA reports)
ENDODONTIC PROCEDURE ( 13 FDA reports)
EXPOSED BONE IN JAW ( 13 FDA reports)
IRON DEFICIENCY ANAEMIA ( 13 FDA reports)
LIFE EXPECTANCY SHORTENED ( 13 FDA reports)
MELANOCYTIC NAEVUS ( 13 FDA reports)
ORAL DISORDER ( 13 FDA reports)
PAIN IN EXTREMITY ( 13 FDA reports)
PERIODONTAL DISEASE ( 13 FDA reports)
RETINAL MELANOMA ( 13 FDA reports)
SENSITIVITY OF TEETH ( 13 FDA reports)
SKIN FIBROSIS ( 13 FDA reports)
SKIN PAPILLOMA ( 13 FDA reports)
STOMATITIS ( 13 FDA reports)
TOOTH LOSS ( 13 FDA reports)
BALANCE DISORDER ( 12 FDA reports)
CARDIAC PACEMAKER INSERTION ( 12 FDA reports)
CATARACT OPERATION ( 12 FDA reports)
COSTOCHONDRITIS ( 12 FDA reports)
MORGANELLA INFECTION ( 12 FDA reports)
NEOPLASM MALIGNANT ( 12 FDA reports)
PALPITATIONS ( 12 FDA reports)
PULMONARY GRANULOMA ( 12 FDA reports)
REFLUX OESOPHAGITIS ( 12 FDA reports)
RENAL FAILURE ACUTE ( 12 FDA reports)
VENOUS INSUFFICIENCY ( 12 FDA reports)
ADJUSTMENT DISORDER WITH MIXED ANXIETY AND DEPRESSED MOOD ( 11 FDA reports)
ADNEXA UTERI CYST ( 11 FDA reports)
ARRHYTHMIA ( 11 FDA reports)
ATRIAL FIBRILLATION ( 11 FDA reports)
BENIGN PROSTATIC HYPERPLASIA ( 11 FDA reports)
BLOOD PRODUCT TRANSFUSION ( 11 FDA reports)
BONE LESION ( 11 FDA reports)
BONE LESION EXCISION ( 11 FDA reports)
CALCULUS URETERIC ( 11 FDA reports)
CONFUSIONAL STATE ( 11 FDA reports)
DYSPLASTIC NAEVUS ( 11 FDA reports)
EYE LASER SURGERY ( 11 FDA reports)
HYDRONEPHROSIS ( 11 FDA reports)
HYDROURETER ( 11 FDA reports)
LIMB OPERATION ( 11 FDA reports)
LUNG NEOPLASM ( 11 FDA reports)
METASTASES TO LIVER ( 11 FDA reports)
MUSCLE INJURY ( 11 FDA reports)
OEDEMA ( 11 FDA reports)
ORAL CANDIDIASIS ( 11 FDA reports)
OSTEOSARCOMA METASTATIC ( 11 FDA reports)
PERICARDIAL EFFUSION ( 11 FDA reports)
SCLERAL OPERATION ( 11 FDA reports)
THYROID CYST ( 11 FDA reports)
UMBILICAL HERNIA REPAIR ( 11 FDA reports)
BLADDER CANCER ( 10 FDA reports)
CHILLS ( 10 FDA reports)
DEAFNESS ( 10 FDA reports)
HYPOTENSION ( 10 FDA reports)
INFLUENZA ( 10 FDA reports)
KERATOCONJUNCTIVITIS SICCA ( 10 FDA reports)
LOSS OF CONSCIOUSNESS ( 10 FDA reports)
MYOPIA ( 10 FDA reports)
RETINAL PIGMENT EPITHELIOPATHY ( 10 FDA reports)
THROAT TIGHTNESS ( 10 FDA reports)
TRICUSPID VALVE INCOMPETENCE ( 10 FDA reports)
CONJUNCTIVITIS ( 9 FDA reports)
DEATH ( 9 FDA reports)
DIABETIC NEUROPATHY ( 9 FDA reports)
FUNGAL INFECTION ( 9 FDA reports)
LEFT ATRIAL DILATATION ( 9 FDA reports)
OSTEONECROSIS ( 9 FDA reports)
PANCREATITIS ( 9 FDA reports)
PEPTIC ULCER ( 9 FDA reports)
RASH GENERALISED ( 9 FDA reports)
RENAL CYST ( 9 FDA reports)
SENSATION OF FOREIGN BODY ( 9 FDA reports)
SEXUALLY TRANSMITTED DISEASE ( 9 FDA reports)
TRANSIENT ISCHAEMIC ATTACK ( 9 FDA reports)
ABDOMINAL DISTENSION ( 8 FDA reports)
BILIARY DYSKINESIA ( 8 FDA reports)
CEREBROVASCULAR ACCIDENT ( 8 FDA reports)
CLOSTRIDIAL INFECTION ( 8 FDA reports)
HOT FLUSH ( 8 FDA reports)
INTRAOCULAR LENS IMPLANT ( 8 FDA reports)
NIGHT SWEATS ( 8 FDA reports)
OTITIS MEDIA ACUTE ( 8 FDA reports)
PRURITUS ( 8 FDA reports)
SEPSIS ( 8 FDA reports)
TENDERNESS ( 8 FDA reports)
THIRST ( 8 FDA reports)
AORTIC VALVE DISEASE ( 7 FDA reports)
BACTERAEMIA ( 7 FDA reports)
BURSITIS ( 7 FDA reports)
CHROMATURIA ( 7 FDA reports)
DENTOFACIAL FUNCTIONAL DISORDER ( 7 FDA reports)
HYPERLIPIDAEMIA ( 7 FDA reports)
HYPERSOMNIA ( 7 FDA reports)
HYPOGLYCAEMIA ( 7 FDA reports)
LEFT VENTRICULAR DYSFUNCTION ( 7 FDA reports)
LETHARGY ( 7 FDA reports)
MALAISE ( 7 FDA reports)
MUSCLE ATROPHY ( 7 FDA reports)
MUSCLE DISORDER ( 7 FDA reports)
PHYSICAL DISABILITY ( 7 FDA reports)
POLYNEUROPATHY ( 7 FDA reports)
PURULENT DISCHARGE ( 7 FDA reports)
SACROILIITIS ( 7 FDA reports)
SICK SINUS SYNDROME ( 7 FDA reports)
SKIN EXFOLIATION ( 7 FDA reports)
SKIN FISSURES ( 7 FDA reports)
SPINAL CORD COMPRESSION ( 7 FDA reports)
SUBACUTE ENDOCARDITIS ( 7 FDA reports)
TINEA PEDIS ( 7 FDA reports)
UROSEPSIS ( 7 FDA reports)
AREFLEXIA ( 6 FDA reports)
ARTHROPOD BITE ( 6 FDA reports)
BLOOD GLUCOSE DECREASED ( 6 FDA reports)
BODY TEMPERATURE DECREASED ( 6 FDA reports)
BURNING SENSATION ( 6 FDA reports)
CONVULSION ( 6 FDA reports)
DISINHIBITION ( 6 FDA reports)
DRUG INTERACTION ( 6 FDA reports)
DRUG WITHDRAWAL SYNDROME ( 6 FDA reports)
DYSPEPSIA ( 6 FDA reports)
EYE OPERATION ( 6 FDA reports)
FAECAL INCONTINENCE ( 6 FDA reports)
GASTRIC ULCER ( 6 FDA reports)
HEPATIC PAIN ( 6 FDA reports)
HIP FRACTURE ( 6 FDA reports)
IRREGULAR SLEEP PHASE ( 6 FDA reports)
MOOD SWINGS ( 6 FDA reports)
MUSCLE TWITCHING ( 6 FDA reports)
NASAL ODOUR ( 6 FDA reports)
OROPHARYNGEAL PAIN ( 6 FDA reports)
PANIC ATTACK ( 6 FDA reports)
PERONEAL NERVE PALSY ( 6 FDA reports)
PHOTOPHOBIA ( 6 FDA reports)
RECTAL HAEMORRHAGE ( 6 FDA reports)
RED BLOOD CELL COUNT DECREASED ( 6 FDA reports)
RESPIRATORY DISTRESS ( 6 FDA reports)
SENSORY LOSS ( 6 FDA reports)
SKIN WARM ( 6 FDA reports)
SLOW RESPONSE TO STIMULI ( 6 FDA reports)
SOMATOSENSORY EVOKED POTENTIALS ABNORMAL ( 6 FDA reports)
STAPHYLOCOCCAL INFECTION ( 6 FDA reports)
SUICIDAL IDEATION ( 6 FDA reports)
TOOTH EXTRACTION ( 6 FDA reports)
CARDIAC DISORDER ( 5 FDA reports)
CENTRAL VENOUS CATHETER REMOVAL ( 5 FDA reports)
CENTRAL VENOUS CATHETERISATION ( 5 FDA reports)
COAGULOPATHY ( 5 FDA reports)
CONTUSION ( 5 FDA reports)
DEBRIDEMENT ( 5 FDA reports)
DIVERTICULUM INTESTINAL ( 5 FDA reports)
DYSARTHRIA ( 5 FDA reports)
ELECTROLYTE IMBALANCE ( 5 FDA reports)
ENDOTRACHEAL INTUBATION ( 5 FDA reports)
FOOT FRACTURE ( 5 FDA reports)
GALLBLADDER DISORDER ( 5 FDA reports)
GALLBLADDER OPERATION ( 5 FDA reports)
HERNIA REPAIR ( 5 FDA reports)
HIP ARTHROPLASTY ( 5 FDA reports)
MEMORY IMPAIRMENT ( 5 FDA reports)
MOOD ALTERED ( 5 FDA reports)
MUSCULOSKELETAL PAIN ( 5 FDA reports)
NEOPLASM SKIN ( 5 FDA reports)
OOPHORECTOMY BILATERAL ( 5 FDA reports)
ORTHOSIS USER ( 5 FDA reports)
SKIN LESION EXCISION ( 5 FDA reports)
SURGERY ( 5 FDA reports)
UPPER-AIRWAY COUGH SYNDROME ( 5 FDA reports)
VERTEBROPLASTY ( 5 FDA reports)
ANOREXIA ( 4 FDA reports)
BRAIN CONTUSION ( 4 FDA reports)
CARDIAC ARREST ( 4 FDA reports)
CARPAL TUNNEL SYNDROME ( 4 FDA reports)
CYSTITIS ( 4 FDA reports)
DIASTOLIC DYSFUNCTION ( 4 FDA reports)
DIPLOPIA ( 4 FDA reports)
DYSPNOEA EXERTIONAL ( 4 FDA reports)
FACET JOINT SYNDROME ( 4 FDA reports)
FEELING HOT ( 4 FDA reports)
FLUID OVERLOAD ( 4 FDA reports)
INCREASED TENDENCY TO BRUISE ( 4 FDA reports)
INJECTION SITE PAIN ( 4 FDA reports)
JOINT DISLOCATION ( 4 FDA reports)
JOINT SWELLING ( 4 FDA reports)
LOWER LIMB FRACTURE ( 4 FDA reports)
MALIGNANT MELANOMA ( 4 FDA reports)
MASTOID DISORDER ( 4 FDA reports)
MUSCULAR WEAKNESS ( 4 FDA reports)
PAIN IN JAW ( 4 FDA reports)
PERITONITIS BACTERIAL ( 4 FDA reports)
PROSTATE CANCER ( 4 FDA reports)
PULMONARY VALVE INCOMPETENCE ( 4 FDA reports)
RENAL FAILURE CHRONIC ( 4 FDA reports)
RESTLESSNESS ( 4 FDA reports)
SECRETION DISCHARGE ( 4 FDA reports)
SLEEP DISORDER ( 4 FDA reports)
SUICIDE ATTEMPT ( 4 FDA reports)
SWOLLEN TONGUE ( 4 FDA reports)
ULCER ( 4 FDA reports)
URINARY TRACT INFECTION ( 4 FDA reports)
ABDOMINAL DISCOMFORT ( 3 FDA reports)
ABNORMAL SENSATION IN EYE ( 3 FDA reports)
ACUTE LYMPHOCYTIC LEUKAEMIA RECURRENT ( 3 FDA reports)
ACUTE SINUSITIS ( 3 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 3 FDA reports)
ARTERIAL BYPASS OPERATION ( 3 FDA reports)
ARTHRITIS ( 3 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 3 FDA reports)
BLADDER CYST ( 3 FDA reports)
BLOOD MAGNESIUM DECREASED ( 3 FDA reports)
BLOOD POTASSIUM DECREASED ( 3 FDA reports)
C-REACTIVE PROTEIN INCREASED ( 3 FDA reports)
CARDIAC FAILURE ( 3 FDA reports)
CELLULITIS STAPHYLOCOCCAL ( 3 FDA reports)
CEREBRAL ATROPHY ( 3 FDA reports)
CERUMEN IMPACTION ( 3 FDA reports)
CHEST DISCOMFORT ( 3 FDA reports)
COCCIDIOIDOMYCOSIS ( 3 FDA reports)
COLD SWEAT ( 3 FDA reports)
COLITIS ( 3 FDA reports)
CYSTOCELE ( 3 FDA reports)
DECUBITUS ULCER ( 3 FDA reports)
DRUG EFFECT DECREASED ( 3 FDA reports)
EAR CONGESTION ( 3 FDA reports)
FACIAL PAIN ( 3 FDA reports)
FLOPPY IRIS SYNDROME ( 3 FDA reports)
GLYCOSYLATED HAEMOGLOBIN INCREASED ( 3 FDA reports)
HAEMATOCHEZIA ( 3 FDA reports)
HAEMOLYSIS ( 3 FDA reports)
HEPATIC LESION ( 3 FDA reports)
HYPERAESTHESIA ( 3 FDA reports)
HYPERGLYCAEMIA ( 3 FDA reports)
INCONTINENCE ( 3 FDA reports)
INJECTION SITE ERYTHEMA ( 3 FDA reports)
LEUKOCYTOSIS ( 3 FDA reports)
LEUKOPENIA ( 3 FDA reports)
LUMBAR SPINAL STENOSIS ( 3 FDA reports)
MASTICATION DISORDER ( 3 FDA reports)
MOBILITY DECREASED ( 3 FDA reports)
MONOCLONAL IMMUNOGLOBULIN PRESENT ( 3 FDA reports)
MUCOSAL INFLAMMATION ( 3 FDA reports)
MUSCLE TIGHTNESS ( 3 FDA reports)
MUSCULOSKELETAL DISCOMFORT ( 3 FDA reports)
MYELODYSPLASTIC SYNDROME ( 3 FDA reports)
MYOCLONUS ( 3 FDA reports)
NAIL OPERATION ( 3 FDA reports)
OBESITY ( 3 FDA reports)
ONYCHOMYCOSIS ( 3 FDA reports)
OSTEITIS ( 3 FDA reports)
OVERDOSE ( 3 FDA reports)
PALLOR ( 3 FDA reports)
PELVIC FRACTURE ( 3 FDA reports)
PHARYNGITIS ( 3 FDA reports)
PLEURITIC PAIN ( 3 FDA reports)
PROGRESSIVE MULTIFOCAL LEUKOENCEPHALOPATHY ( 3 FDA reports)
PSYCHOMOTOR HYPERACTIVITY ( 3 FDA reports)
PULMONARY EMBOLISM ( 3 FDA reports)
PULMONARY OEDEMA ( 3 FDA reports)
RASH ( 3 FDA reports)
RECTOCELE ( 3 FDA reports)
SCAR ( 3 FDA reports)
STATUS EPILEPTICUS ( 3 FDA reports)
SWELLING FACE ( 3 FDA reports)
TACHYCARDIA ( 3 FDA reports)
TEMPOROMANDIBULAR JOINT SYNDROME ( 3 FDA reports)
THROMBOSIS IN DEVICE ( 3 FDA reports)
TOOTH FRACTURE ( 3 FDA reports)
UPPER RESPIRATORY TRACT INFECTION ( 3 FDA reports)
VENOUS THROMBOSIS LIMB ( 3 FDA reports)
VITAMIN D DEFICIENCY ( 3 FDA reports)
ABSCESS LIMB ( 2 FDA reports)
ACNE ( 2 FDA reports)
ADRENAL INSUFFICIENCY ( 2 FDA reports)
ALOPECIA ( 2 FDA reports)
ALTERED STATE OF CONSCIOUSNESS ( 2 FDA reports)
ANORECTAL DISCOMFORT ( 2 FDA reports)
ANOXIC ENCEPHALOPATHY ( 2 FDA reports)
ATRIAL FLUTTER ( 2 FDA reports)
BIOPSY BONE ( 2 FDA reports)
BLINDNESS ( 2 FDA reports)
BLOOD SODIUM DECREASED ( 2 FDA reports)
BLOOD VISCOSITY INCREASED ( 2 FDA reports)
BONE DEBRIDEMENT ( 2 FDA reports)
BRONCHOSPASM ( 2 FDA reports)
BUNDLE BRANCH BLOCK LEFT ( 2 FDA reports)
CARDIAC ENZYMES INCREASED ( 2 FDA reports)
CATHETER SITE HAEMATOMA ( 2 FDA reports)
CHOLECYSTITIS CHRONIC ( 2 FDA reports)
COLITIS ISCHAEMIC ( 2 FDA reports)
DENTAL OPERATION ( 2 FDA reports)
DIABETES MELLITUS INADEQUATE CONTROL ( 2 FDA reports)
DIABETIC COMA ( 2 FDA reports)
DIABETIC RETINOPATHY ( 2 FDA reports)
DRUG HYPERSENSITIVITY ( 2 FDA reports)
DRUG LEVEL INCREASED ( 2 FDA reports)
DRUG TOLERANCE DECREASED ( 2 FDA reports)
DYSPHONIA ( 2 FDA reports)
DYSPLASTIC NAEVUS SYNDROME ( 2 FDA reports)
DYSSTASIA ( 2 FDA reports)
ECONOMIC PROBLEM ( 2 FDA reports)
ELECTROCARDIOGRAM QT PROLONGED ( 2 FDA reports)
EPISTAXIS ( 2 FDA reports)
EXTRAOCULAR MUSCLE PARESIS ( 2 FDA reports)
EYE DISORDER ( 2 FDA reports)
EYE HAEMORRHAGE ( 2 FDA reports)
FEBRILE NEUTROPENIA ( 2 FDA reports)
FEMUR FRACTURE ( 2 FDA reports)
GASTRITIS EROSIVE ( 2 FDA reports)
GASTROINTESTINAL HAEMORRHAGE ( 2 FDA reports)
GENERAL PHYSICAL CONDITION ABNORMAL ( 2 FDA reports)
GLOMERULAR FILTRATION RATE DECREASED ( 2 FDA reports)
HALLUCINATION, AUDITORY ( 2 FDA reports)
HEART RATE IRREGULAR ( 2 FDA reports)
HYPOGLYCAEMIC UNCONSCIOUSNESS ( 2 FDA reports)
HYPOVITAMINOSIS ( 2 FDA reports)
INFLUENZA LIKE ILLNESS ( 2 FDA reports)
INITIAL INSOMNIA ( 2 FDA reports)
INJECTION SITE BRUISING ( 2 FDA reports)
IRON OVERLOAD ( 2 FDA reports)
IRRITABLE BOWEL SYNDROME ( 2 FDA reports)
JOINT CREPITATION ( 2 FDA reports)
LUNG INFECTION ( 2 FDA reports)
LYMPHADENOPATHY ( 2 FDA reports)
MASS ( 2 FDA reports)
MENSTRUATION IRREGULAR ( 2 FDA reports)
MENTAL DISORDER ( 2 FDA reports)
MIDDLE INSOMNIA ( 2 FDA reports)
MITRAL VALVE PROLAPSE ( 2 FDA reports)
MUSCULOSKELETAL CHEST PAIN ( 2 FDA reports)
NASAL DRYNESS ( 2 FDA reports)
NECROTISING FASCIITIS ( 2 FDA reports)
NEURALGIA ( 2 FDA reports)
NEUTROPENIA ( 2 FDA reports)
NEUTROPHIL COUNT DECREASED ( 2 FDA reports)
OESOPHAGITIS ULCERATIVE ( 2 FDA reports)
OPTIC NEURITIS ( 2 FDA reports)
PAPILLARY THYROID CANCER ( 2 FDA reports)
PARANASAL SINUS HYPERSECRETION ( 2 FDA reports)
PARESIS ( 2 FDA reports)
PHOTOSENSITIVITY REACTION ( 2 FDA reports)
POST PROCEDURAL HAEMORRHAGE ( 2 FDA reports)
POSTOPERATIVE RESPIRATORY DISTRESS ( 2 FDA reports)
PSORIASIS ( 2 FDA reports)
RADIATION PNEUMONITIS ( 2 FDA reports)
RED BLOOD CELL SEDIMENTATION RATE INCREASED ( 2 FDA reports)
REFRACTORINESS TO PLATELET TRANSFUSION ( 2 FDA reports)
RESPIRATORY FAILURE ( 2 FDA reports)
RHABDOMYOLYSIS ( 2 FDA reports)
RHINORRHOEA ( 2 FDA reports)
SCOLIOSIS ( 2 FDA reports)
SEROMA ( 2 FDA reports)
SINUS DISORDER ( 2 FDA reports)
SKIN DISCOLOURATION ( 2 FDA reports)
SKIN HAEMORRHAGE ( 2 FDA reports)
SNEEZING ( 2 FDA reports)
SPEECH DISORDER ( 2 FDA reports)
SPINAL FRACTURE ( 2 FDA reports)
THYROID CANCER ( 2 FDA reports)
THYROID NEOPLASM ( 2 FDA reports)
TREATMENT NONCOMPLIANCE ( 2 FDA reports)
VEIN DISORDER ( 2 FDA reports)
VIRAL INFECTION ( 2 FDA reports)
VISUAL IMPAIRMENT ( 2 FDA reports)
WHITE BLOOD CELL COUNT DECREASED ( 2 FDA reports)
WOUND ( 2 FDA reports)
WOUND TREATMENT ( 2 FDA reports)
ACCIDENT ( 1 FDA reports)
ACUTE MYELOID LEUKAEMIA ( 1 FDA reports)
ALPHA 1 GLOBULIN INCREASED ( 1 FDA reports)
ALPHA 2 GLOBULIN INCREASED ( 1 FDA reports)
ALVEOLITIS ALLERGIC ( 1 FDA reports)
AMMONIA INCREASED ( 1 FDA reports)
ANAPHYLACTIC REACTION ( 1 FDA reports)
ANHEDONIA ( 1 FDA reports)
AORTIC CALCIFICATION ( 1 FDA reports)
AORTIC DISORDER ( 1 FDA reports)
APPLICATION SITE PAIN ( 1 FDA reports)
BALANITIS ( 1 FDA reports)
BEDRIDDEN ( 1 FDA reports)
BLOOD ALKALINE PHOSPHATASE INCREASED ( 1 FDA reports)
BLOOD CALCIUM DECREASED ( 1 FDA reports)
BLOOD CHOLESTEROL ABNORMAL ( 1 FDA reports)
BLOOD CREATININE INCREASED ( 1 FDA reports)
BLOOD GLUCOSE FLUCTUATION ( 1 FDA reports)
BLOOD PRESSURE FLUCTUATION ( 1 FDA reports)
BLOOD URINE PRESENT ( 1 FDA reports)
BODY TEMPERATURE FLUCTUATION ( 1 FDA reports)
BONE GRAFT ( 1 FDA reports)
BONE LOSS ( 1 FDA reports)
BREAST CANCER ( 1 FDA reports)
BREAST CANCER FEMALE ( 1 FDA reports)
CARDIAC OPERATION ( 1 FDA reports)
CAROTID ARTERY OCCLUSION ( 1 FDA reports)
CATHETER SITE ERYTHEMA ( 1 FDA reports)
CEREBRAL INFARCTION ( 1 FDA reports)
CHOLECYSTECTOMY ( 1 FDA reports)
COLLAPSE OF LUNG ( 1 FDA reports)
COLONOSCOPY ( 1 FDA reports)
COMPLEX PARTIAL SEIZURES ( 1 FDA reports)
CONCOMITANT DISEASE AGGRAVATED ( 1 FDA reports)
CONDITION AGGRAVATED ( 1 FDA reports)
CONDUCTION DISORDER ( 1 FDA reports)
CORNEAL OEDEMA ( 1 FDA reports)
CORNEAL OPACITY ( 1 FDA reports)
CYANOSIS ( 1 FDA reports)
DEPENDENCE ON RESPIRATOR ( 1 FDA reports)
DEVICE MALFUNCTION ( 1 FDA reports)
DEVICE RELATED INFECTION ( 1 FDA reports)
DEVICE RELATED SEPSIS ( 1 FDA reports)
DIABETIC ULCER ( 1 FDA reports)
DIALYSIS ( 1 FDA reports)
DISORIENTATION ( 1 FDA reports)
DRUG ADMINISTRATION ERROR ( 1 FDA reports)
DRUG DOSE OMISSION ( 1 FDA reports)
DRUG PRESCRIBING ERROR ( 1 FDA reports)
DYSKINESIA ( 1 FDA reports)
ELECTROCARDIOGRAM QRS COMPLEX PROLONGED ( 1 FDA reports)
ELECTROCARDIOGRAM ST SEGMENT ABNORMAL ( 1 FDA reports)
EMOTIONAL DISORDER ( 1 FDA reports)
ENDOTRACHEAL INTUBATION COMPLICATION ( 1 FDA reports)
ERUCTATION ( 1 FDA reports)
EXERCISE TOLERANCE DECREASED ( 1 FDA reports)
EYE DISCHARGE ( 1 FDA reports)
EYE INFECTION ( 1 FDA reports)
EYE PRURITUS ( 1 FDA reports)
EYELID INFECTION ( 1 FDA reports)
FACIAL PALSY ( 1 FDA reports)
FAECES DISCOLOURED ( 1 FDA reports)
FAECES HARD ( 1 FDA reports)
FEAR ( 1 FDA reports)
FEELING COLD ( 1 FDA reports)
FEELING OF BODY TEMPERATURE CHANGE ( 1 FDA reports)
FIBROMYALGIA ( 1 FDA reports)
FIBROSIS ( 1 FDA reports)
FIBULA FRACTURE ( 1 FDA reports)
FLATULENCE ( 1 FDA reports)
FLUID RETENTION ( 1 FDA reports)
FOOD AVERSION ( 1 FDA reports)
GALLBLADDER ENLARGEMENT ( 1 FDA reports)
GAMMA-GLUTAMYLTRANSFERASE INCREASED ( 1 FDA reports)
GASTRIC ULCER HAEMORRHAGE ( 1 FDA reports)
GASTROINTESTINAL DISORDER ( 1 FDA reports)
GINGIVAL BLEEDING ( 1 FDA reports)
GINGIVITIS ( 1 FDA reports)
GLOBAL AMNESIA ( 1 FDA reports)
GRAND MAL CONVULSION ( 1 FDA reports)
HAEMANGIOMA OF LIVER ( 1 FDA reports)
HAEMODIALYSIS ( 1 FDA reports)
HAEMOPTYSIS ( 1 FDA reports)
HEMIPARESIS ( 1 FDA reports)
HEPATIC ENZYME INCREASED ( 1 FDA reports)
HEPATOMEGALY ( 1 FDA reports)
HYPERCHLORHYDRIA ( 1 FDA reports)
HYPERKALAEMIA ( 1 FDA reports)
HYPERURICAEMIA ( 1 FDA reports)
HYPOAESTHESIA ORAL ( 1 FDA reports)
HYPOGLYCAEMIC SEIZURE ( 1 FDA reports)
HYPOTONIA ( 1 FDA reports)
HYPOXIA ( 1 FDA reports)
HYPOXIC-ISCHAEMIC ENCEPHALOPATHY ( 1 FDA reports)
IIIRD NERVE PARALYSIS ( 1 FDA reports)
IMMOBILE ( 1 FDA reports)
IMPAIRED DRIVING ABILITY ( 1 FDA reports)
IMPAIRED HEALING ( 1 FDA reports)
IMPAIRED WORK ABILITY ( 1 FDA reports)
INCORRECT DOSE ADMINISTERED ( 1 FDA reports)
INCREASED UPPER AIRWAY SECRETION ( 1 FDA reports)
INFLAMMATION ( 1 FDA reports)
INFLAMMATORY MARKER INCREASED ( 1 FDA reports)
INJECTION SITE FIBROSIS ( 1 FDA reports)
INJECTION SITE HAEMATOMA ( 1 FDA reports)
INJECTION SITE PRURITUS ( 1 FDA reports)
INJECTION SITE SCAR ( 1 FDA reports)
INTERSTITIAL LUNG DISEASE ( 1 FDA reports)
INTERVERTEBRAL DISC COMPRESSION ( 1 FDA reports)
INTERVERTEBRAL DISC DISORDER ( 1 FDA reports)
INTESTINAL MUCOSAL HYPERTROPHY ( 1 FDA reports)
INVESTIGATION ( 1 FDA reports)
IRITIS ( 1 FDA reports)
JAW FRACTURE ( 1 FDA reports)
JOINT EFFUSION ( 1 FDA reports)
JOINT SPRAIN ( 1 FDA reports)
JOINT STIFFNESS ( 1 FDA reports)
KNEE ARTHROPLASTY ( 1 FDA reports)
KYPHOSIS ( 1 FDA reports)
LACRIMATION INCREASED ( 1 FDA reports)
LEUKAEMIA ( 1 FDA reports)
LOCAL SWELLING ( 1 FDA reports)
LYME DISEASE ( 1 FDA reports)
LYMPHOCYTE COUNT DECREASED ( 1 FDA reports)
MALNUTRITION ( 1 FDA reports)
MANIA ( 1 FDA reports)
MEDICATION ERROR ( 1 FDA reports)
MEIBOMIANITIS ( 1 FDA reports)
MENORRHAGIA ( 1 FDA reports)
METABOLIC ACIDOSIS ( 1 FDA reports)
METASTASES TO EYE ( 1 FDA reports)
METRORRHAGIA ( 1 FDA reports)
MIGRAINE ( 1 FDA reports)
MIXED CONNECTIVE TISSUE DISEASE ( 1 FDA reports)
MOTOR DYSFUNCTION ( 1 FDA reports)
MULTIPLE SCLEROSIS ( 1 FDA reports)
MULTIPLE SCLEROSIS RELAPSE ( 1 FDA reports)
MYOCARDIAL INFARCTION ( 1 FDA reports)
NASAL CONGESTION ( 1 FDA reports)
NEOPLASM PROGRESSION ( 1 FDA reports)
NEPHROGENIC ANAEMIA ( 1 FDA reports)
NEPHROTIC SYNDROME ( 1 FDA reports)
NEUTROPENIC SEPSIS ( 1 FDA reports)
NIGHTMARE ( 1 FDA reports)
NO ADVERSE EVENT ( 1 FDA reports)
NON-SMALL CELL LUNG CANCER RECURRENT ( 1 FDA reports)
OFF LABEL USE ( 1 FDA reports)
ORAL HERPES ( 1 FDA reports)
ORAL INFECTION ( 1 FDA reports)
OTORRHOEA ( 1 FDA reports)
OXYGEN SATURATION DECREASED ( 1 FDA reports)
PARKINSONIAN GAIT ( 1 FDA reports)
PENILE NECROSIS ( 1 FDA reports)
PENIS DISORDER ( 1 FDA reports)
PERIORBITAL CELLULITIS ( 1 FDA reports)
PERIPHERAL COLDNESS ( 1 FDA reports)
PERITONEAL DIALYSIS COMPLICATION ( 1 FDA reports)
PHARMACEUTICAL PRODUCT COMPLAINT ( 1 FDA reports)
PLEURISY ( 1 FDA reports)
PNEUMONITIS ( 1 FDA reports)
POISONING ( 1 FDA reports)
POLLAKIURIA ( 1 FDA reports)
POLYMYALGIA RHEUMATICA ( 1 FDA reports)
POOR QUALITY SLEEP ( 1 FDA reports)
POST PROCEDURAL COMPLICATION ( 1 FDA reports)
POSTMENOPAUSE ( 1 FDA reports)
PROTEIN TOTAL DECREASED ( 1 FDA reports)
PUBIC RAMI FRACTURE ( 1 FDA reports)
PUBIS FRACTURE ( 1 FDA reports)
PULMONARY CALCIFICATION ( 1 FDA reports)
PULMONARY FIBROSIS ( 1 FDA reports)
QUALITY OF LIFE DECREASED ( 1 FDA reports)
REBOUND EFFECT ( 1 FDA reports)
RENAL TUBULAR NECROSIS ( 1 FDA reports)
RESPIRATORY ARREST ( 1 FDA reports)
RETINAL ARTERY OCCLUSION ( 1 FDA reports)
RETINAL TEAR ( 1 FDA reports)
ROTATOR CUFF SYNDROME ( 1 FDA reports)
SCOTOMA ( 1 FDA reports)
SCRATCH ( 1 FDA reports)
SEASONAL ALLERGY ( 1 FDA reports)
SEDATION ( 1 FDA reports)
SENSATION OF HEAVINESS ( 1 FDA reports)
SENSORY DISTURBANCE ( 1 FDA reports)
SEPTIC SHOCK ( 1 FDA reports)
SINUS TACHYCARDIA ( 1 FDA reports)
SKIN LACERATION ( 1 FDA reports)
SKIN LESION ( 1 FDA reports)
SLEEP APNOEA SYNDROME ( 1 FDA reports)
SOMNAMBULISM ( 1 FDA reports)
STEVENS-JOHNSON SYNDROME ( 1 FDA reports)
STOMACH DISCOMFORT ( 1 FDA reports)
STREPTOBACILLUS INFECTION ( 1 FDA reports)
STREPTOCOCCAL SEPSIS ( 1 FDA reports)
STRESS ( 1 FDA reports)
SUBCUTANEOUS ABSCESS ( 1 FDA reports)
SUPERFICIAL INJURY OF EYE ( 1 FDA reports)
SYSTEMIC LUPUS ERYTHEMATOSUS ( 1 FDA reports)
TENDON RUPTURE ( 1 FDA reports)
THERAPEUTIC RESPONSE UNEXPECTED WITH DRUG SUBSTITUTION ( 1 FDA reports)
THINKING ABNORMAL ( 1 FDA reports)
TINEA INFECTION ( 1 FDA reports)
TONIC CLONIC MOVEMENTS ( 1 FDA reports)
TOOTH ABSCESS ( 1 FDA reports)
TOOTH DISORDER ( 1 FDA reports)
UNDERDOSE ( 1 FDA reports)
UNDERWEIGHT ( 1 FDA reports)
UNEVALUABLE EVENT ( 1 FDA reports)
UNRESPONSIVE TO STIMULI ( 1 FDA reports)
URINARY CASTS ( 1 FDA reports)
URINARY INCONTINENCE ( 1 FDA reports)
URINE LEUKOCYTE ESTERASE POSITIVE ( 1 FDA reports)
VASCULAR CALCIFICATION ( 1 FDA reports)
VENTRICULAR EXTRASYSTOLES ( 1 FDA reports)
VENTRICULAR FIBRILLATION ( 1 FDA reports)
VERTEBRAL FORAMINAL STENOSIS ( 1 FDA reports)
VESSEL PERFORATION ( 1 FDA reports)
VIITH NERVE PARALYSIS ( 1 FDA reports)
VISUAL FIELD DEFECT ( 1 FDA reports)
VITH NERVE PARALYSIS ( 1 FDA reports)
WEIGHT FLUCTUATION ( 1 FDA reports)
WHITE BLOOD CELLS URINE POSITIVE ( 1 FDA reports)

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