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

PAIN ( 142 FDA reports)
ARTHRALGIA ( 138 FDA reports)
DYSPNOEA ( 122 FDA reports)
HEADACHE ( 118 FDA reports)
NAUSEA ( 111 FDA reports)
OSTEONECROSIS ( 110 FDA reports)
OSTEONECROSIS OF JAW ( 100 FDA reports)
BACK PAIN ( 96 FDA reports)
FATIGUE ( 88 FDA reports)
METASTASES TO BONE ( 87 FDA reports)
CHEST PAIN ( 82 FDA reports)
OSTEOMYELITIS ( 81 FDA reports)
VOMITING ( 81 FDA reports)
DEPRESSION ( 75 FDA reports)
PAIN IN EXTREMITY ( 75 FDA reports)
DIZZINESS ( 74 FDA reports)
PAIN IN JAW ( 74 FDA reports)
ABDOMINAL PAIN ( 71 FDA reports)
TOOTH EXTRACTION ( 69 FDA reports)
DIARRHOEA ( 68 FDA reports)
GENERAL PHYSICAL HEALTH DETERIORATION ( 67 FDA reports)
WEIGHT DECREASED ( 66 FDA reports)
ANXIETY ( 65 FDA reports)
ASTHENIA ( 65 FDA reports)
BONE DISORDER ( 64 FDA reports)
BREAST CANCER ( 62 FDA reports)
OEDEMA PERIPHERAL ( 62 FDA reports)
FALL ( 61 FDA reports)
ANAEMIA ( 59 FDA reports)
INSOMNIA ( 59 FDA reports)
CONSTIPATION ( 56 FDA reports)
HYPERTENSION ( 55 FDA reports)
HYPOTENSION ( 55 FDA reports)
OSTEOARTHRITIS ( 54 FDA reports)
IMPAIRED HEALING ( 53 FDA reports)
GASTROOESOPHAGEAL REFLUX DISEASE ( 52 FDA reports)
PLEURAL EFFUSION ( 52 FDA reports)
DRUG INTERACTION ( 51 FDA reports)
PNEUMONIA ( 50 FDA reports)
PNEUMOTHORAX ( 49 FDA reports)
INFECTION ( 47 FDA reports)
ALOPECIA ( 46 FDA reports)
GASTROINTESTINAL HAEMORRHAGE ( 46 FDA reports)
HYPOAESTHESIA ( 46 FDA reports)
ERYTHEMA ( 45 FDA reports)
METASTASES TO CENTRAL NERVOUS SYSTEM ( 45 FDA reports)
COUGH ( 44 FDA reports)
HYPOKALAEMIA ( 44 FDA reports)
INTERVERTEBRAL DISC DEGENERATION ( 44 FDA reports)
LOCALISED INFECTION ( 43 FDA reports)
PYREXIA ( 43 FDA reports)
VISION BLURRED ( 43 FDA reports)
CHRONIC OBSTRUCTIVE PULMONARY DISEASE ( 42 FDA reports)
HOT FLUSH ( 42 FDA reports)
SYNCOPE ( 41 FDA reports)
URINARY TRACT INFECTION ( 41 FDA reports)
BONE PAIN ( 40 FDA reports)
INJURY ( 39 FDA reports)
FEELING ABNORMAL ( 38 FDA reports)
DENTAL CARIES ( 37 FDA reports)
SWELLING ( 37 FDA reports)
LOOSE TOOTH ( 36 FDA reports)
ARTERIOSCLEROSIS ( 35 FDA reports)
BRONCHITIS ( 35 FDA reports)
DRUG INEFFECTIVE ( 35 FDA reports)
DYSPHAGIA ( 35 FDA reports)
MUSCULOSKELETAL CHEST PAIN ( 35 FDA reports)
SINUSITIS ( 35 FDA reports)
EAR PAIN ( 34 FDA reports)
MYALGIA ( 34 FDA reports)
OSTEOPOROSIS ( 34 FDA reports)
PULMONARY EMBOLISM ( 34 FDA reports)
DECREASED APPETITE ( 33 FDA reports)
EMOTIONAL DISTRESS ( 33 FDA reports)
GAIT DISTURBANCE ( 33 FDA reports)
LUNG NEOPLASM ( 33 FDA reports)
MYOCARDIAL INFARCTION ( 33 FDA reports)
OSTEOPENIA ( 33 FDA reports)
PARAESTHESIA ( 33 FDA reports)
SOMNOLENCE ( 33 FDA reports)
ARTHROPATHY ( 32 FDA reports)
CONFUSIONAL STATE ( 32 FDA reports)
DEVICE RELATED INFECTION ( 32 FDA reports)
BREAST CANCER METASTATIC ( 31 FDA reports)
DIABETES MELLITUS ( 31 FDA reports)
GINGIVAL INFECTION ( 31 FDA reports)
HAEMORRHOIDS ( 31 FDA reports)
RENAL FAILURE ACUTE ( 31 FDA reports)
TOOTHACHE ( 31 FDA reports)
ARTHRITIS ( 30 FDA reports)
COMPUTERISED TOMOGRAM ABNORMAL ( 30 FDA reports)
DEEP VEIN THROMBOSIS ( 30 FDA reports)
METASTASES TO LIVER ( 30 FDA reports)
ORAL PAIN ( 29 FDA reports)
PALPITATIONS ( 29 FDA reports)
RECTAL HAEMORRHAGE ( 29 FDA reports)
FACE AND MOUTH X-RAY ABNORMAL ( 27 FDA reports)
TINNITUS ( 27 FDA reports)
BREAST CANCER RECURRENT ( 26 FDA reports)
CELLULITIS ( 26 FDA reports)
CORONARY ARTERY DISEASE ( 26 FDA reports)
DRY MOUTH ( 26 FDA reports)
EXPOSED BONE IN JAW ( 26 FDA reports)
NEUTROPENIA ( 26 FDA reports)
NIGHT SWEATS ( 26 FDA reports)
SWELLING FACE ( 26 FDA reports)
DECREASED INTEREST ( 25 FDA reports)
DISEASE PROGRESSION ( 25 FDA reports)
PULMONARY FIBROSIS ( 25 FDA reports)
TACHYCARDIA ( 25 FDA reports)
TREMOR ( 25 FDA reports)
ASTHMA ( 24 FDA reports)
HYPONATRAEMIA ( 24 FDA reports)
MALIGNANT NEOPLASM PROGRESSION ( 24 FDA reports)
MUSCLE SPASMS ( 24 FDA reports)
OSTEITIS ( 24 FDA reports)
THROMBOCYTOPENIA ( 24 FDA reports)
BLOOD PRESSURE INCREASED ( 23 FDA reports)
BONE DEBRIDEMENT ( 23 FDA reports)
HAEMATURIA ( 23 FDA reports)
OSTEOSCLEROSIS ( 23 FDA reports)
RENAL FAILURE ( 23 FDA reports)
WEIGHT INCREASED ( 23 FDA reports)
CARDIAC FAILURE CONGESTIVE ( 22 FDA reports)
CHILLS ( 22 FDA reports)
HYDRONEPHROSIS ( 22 FDA reports)
NEOPLASM MALIGNANT ( 22 FDA reports)
PRODUCT SUBSTITUTION ISSUE ( 22 FDA reports)
PURULENT DISCHARGE ( 22 FDA reports)
SUICIDAL IDEATION ( 22 FDA reports)
TENDERNESS ( 22 FDA reports)
ABDOMINAL PAIN UPPER ( 21 FDA reports)
DEATH ( 21 FDA reports)
HYPERCHOLESTEROLAEMIA ( 21 FDA reports)
LOSS OF CONSCIOUSNESS ( 21 FDA reports)
MALAISE ( 21 FDA reports)
MUSCULOSKELETAL PAIN ( 21 FDA reports)
BONE SCAN ABNORMAL ( 20 FDA reports)
DEHYDRATION ( 20 FDA reports)
GINGIVAL RECESSION ( 20 FDA reports)
METASTASES TO LUNG ( 20 FDA reports)
MIGRAINE ( 20 FDA reports)
OESOPHAGITIS ( 20 FDA reports)
RADIUS FRACTURE ( 20 FDA reports)
TUMOUR MARKER INCREASED ( 20 FDA reports)
AGRANULOCYTOSIS ( 19 FDA reports)
BLOOD CHOLESTEROL INCREASED ( 19 FDA reports)
BLOOD GLUCOSE INCREASED ( 19 FDA reports)
DEFORMITY ( 19 FDA reports)
DELIRIUM ( 19 FDA reports)
DEPRESSIVE SYMPTOM ( 19 FDA reports)
DEVICE FAILURE ( 19 FDA reports)
GINGIVAL OEDEMA ( 19 FDA reports)
HYPERCOAGULATION ( 19 FDA reports)
JOINT SWELLING ( 19 FDA reports)
LEUKOPENIA ( 19 FDA reports)
MUSCULOSKELETAL STIFFNESS ( 19 FDA reports)
SYNOVIAL CYST ( 19 FDA reports)
VAGINAL INFECTION ( 19 FDA reports)
CONVULSION ( 18 FDA reports)
FISTULA ( 18 FDA reports)
GINGIVAL SWELLING ( 18 FDA reports)
HAEMOGLOBIN DECREASED ( 18 FDA reports)
HYPERHIDROSIS ( 18 FDA reports)
STREPTOCOCCAL INFECTION ( 18 FDA reports)
VENOUS INSUFFICIENCY ( 18 FDA reports)
ADVERSE DRUG REACTION ( 17 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 17 FDA reports)
ANHEDONIA ( 17 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 17 FDA reports)
COMPRESSION FRACTURE ( 17 FDA reports)
EJECTION FRACTION DECREASED ( 17 FDA reports)
HAEMATOCHEZIA ( 17 FDA reports)
ILEUS PARALYTIC ( 17 FDA reports)
MEMORY IMPAIRMENT ( 17 FDA reports)
PRURITUS ( 17 FDA reports)
PULMONARY CONGESTION ( 17 FDA reports)
SEBORRHOEIC KERATOSIS ( 17 FDA reports)
SPINAL DISORDER ( 17 FDA reports)
BRONCHOSPASM ( 16 FDA reports)
CHRONIC SINUSITIS ( 16 FDA reports)
EMPHYSEMA ( 16 FDA reports)
FACIAL PAIN ( 16 FDA reports)
INTERVERTEBRAL DISC PROTRUSION ( 16 FDA reports)
JOINT EFFUSION ( 16 FDA reports)
LETHARGY ( 16 FDA reports)
MITRAL VALVE INCOMPETENCE ( 16 FDA reports)
NEUROPATHY PERIPHERAL ( 16 FDA reports)
OEDEMA MOUTH ( 16 FDA reports)
PELVIC PAIN ( 16 FDA reports)
RASH ( 16 FDA reports)
SEPSIS ( 16 FDA reports)
SPINAL DEFORMITY ( 16 FDA reports)
STAPHYLOCOCCAL INFECTION ( 16 FDA reports)
TENDON DISORDER ( 16 FDA reports)
TOOTH ABSCESS ( 16 FDA reports)
TRICUSPID VALVE INCOMPETENCE ( 16 FDA reports)
ABDOMINAL DISCOMFORT ( 15 FDA reports)
ANGINA PECTORIS ( 15 FDA reports)
BLOOD CREATININE INCREASED ( 15 FDA reports)
CARDIAC DISORDER ( 15 FDA reports)
DIVERTICULUM ( 15 FDA reports)
DYSPHONIA ( 15 FDA reports)
FEBRILE NEUTROPENIA ( 15 FDA reports)
GLOSSODYNIA ( 15 FDA reports)
HEART RATE INCREASED ( 15 FDA reports)
HYPERSENSITIVITY ( 15 FDA reports)
MYOCARDIAL ISCHAEMIA ( 15 FDA reports)
NEOPLASM PROGRESSION ( 15 FDA reports)
ORAL CANDIDIASIS ( 15 FDA reports)
OVERDOSE ( 15 FDA reports)
PLATELET COUNT DECREASED ( 15 FDA reports)
SEQUESTRECTOMY ( 15 FDA reports)
SLEEP DISORDER ( 15 FDA reports)
SPINAL OSTEOARTHRITIS ( 15 FDA reports)
BONE ATROPHY ( 14 FDA reports)
CARDIOMEGALY ( 14 FDA reports)
DEPRESSED MOOD ( 14 FDA reports)
DYSKINESIA ( 14 FDA reports)
DYSURIA ( 14 FDA reports)
FOOT FRACTURE ( 14 FDA reports)
GINGIVITIS ( 14 FDA reports)
HYPERGLYCAEMIA ( 14 FDA reports)
LIVER FUNCTION TEST ABNORMAL ( 14 FDA reports)
METASTASIS ( 14 FDA reports)
MOOD SWINGS ( 14 FDA reports)
SENSATION OF PRESSURE ( 14 FDA reports)
SINUS TACHYCARDIA ( 14 FDA reports)
SKIN LESION ( 14 FDA reports)
SURGERY ( 14 FDA reports)
WHITE BLOOD CELL COUNT INCREASED ( 14 FDA reports)
ABSCESS ( 13 FDA reports)
ANGIOMYOLIPOMA ( 13 FDA reports)
BLOOD GLUCOSE DECREASED ( 13 FDA reports)
BLOOD UREA INCREASED ( 13 FDA reports)
BONE GRAFT ( 13 FDA reports)
BUNION ( 13 FDA reports)
CUTANEOUS VASCULITIS ( 13 FDA reports)
GINGIVAL ERYTHEMA ( 13 FDA reports)
GRANULOMA ( 13 FDA reports)
HEPATIC STEATOSIS ( 13 FDA reports)
HERPES ZOSTER ( 13 FDA reports)
HYPERBARIC OXYGEN THERAPY ( 13 FDA reports)
LYMPHOEDEMA ( 13 FDA reports)
MENOPAUSAL SYMPTOMS ( 13 FDA reports)
PANCYTOPENIA ( 13 FDA reports)
PECTUS EXCAVATUM ( 13 FDA reports)
RASH PRURITIC ( 13 FDA reports)
RHINITIS ( 13 FDA reports)
SUDDEN DEATH ( 13 FDA reports)
TENDONITIS ( 13 FDA reports)
VARICOSE VEIN ( 13 FDA reports)
WHEEZING ( 13 FDA reports)
ASCITES ( 12 FDA reports)
CARDIAC FAILURE ( 12 FDA reports)
COLONIC POLYP ( 12 FDA reports)
DIVERTICULUM INTESTINAL ( 12 FDA reports)
DYSPEPSIA ( 12 FDA reports)
LOCAL SWELLING ( 12 FDA reports)
MASS ( 12 FDA reports)
MELANOCYTIC NAEVUS ( 12 FDA reports)
MIDDLE INSOMNIA ( 12 FDA reports)
NECK PAIN ( 12 FDA reports)
ORAL INFECTION ( 12 FDA reports)
PLEURAL FIBROSIS ( 12 FDA reports)
UPPER RESPIRATORY TRACT INFECTION ( 12 FDA reports)
WHITE BLOOD CELL COUNT DECREASED ( 12 FDA reports)
X-RAY ABNORMAL ( 12 FDA reports)
ABDOMINAL DISTENSION ( 11 FDA reports)
ABNORMAL DREAMS ( 11 FDA reports)
ANOGENITAL WARTS ( 11 FDA reports)
BURNING SENSATION ( 11 FDA reports)
BURSITIS ( 11 FDA reports)
CHANGE OF BOWEL HABIT ( 11 FDA reports)
COLONOSCOPY ABNORMAL ( 11 FDA reports)
COMPUTERISED TOMOGRAM ABDOMEN ABNORMAL ( 11 FDA reports)
COMPUTERISED TOMOGRAM THORAX ABNORMAL ( 11 FDA reports)
CONDITION AGGRAVATED ( 11 FDA reports)
DRUG INTOLERANCE ( 11 FDA reports)
HAEMANGIOMA ( 11 FDA reports)
HAEMORRHAGE ( 11 FDA reports)
HEPATIC FUNCTION ABNORMAL ( 11 FDA reports)
JOINT STIFFNESS ( 11 FDA reports)
LUNG NEOPLASM MALIGNANT ( 11 FDA reports)
MENORRHAGIA ( 11 FDA reports)
METASTATIC NEOPLASM ( 11 FDA reports)
MUSCLE ATROPHY ( 11 FDA reports)
MUSCULAR WEAKNESS ( 11 FDA reports)
NEURODERMATITIS ( 11 FDA reports)
NIGHTMARE ( 11 FDA reports)
OROPHARYNGEAL PAIN ( 11 FDA reports)
OTITIS MEDIA ( 11 FDA reports)
OVARIAN MASS ( 11 FDA reports)
PERICARDIAL EFFUSION ( 11 FDA reports)
PERIPHERAL VASCULAR DISORDER ( 11 FDA reports)
POSITRON EMISSION TOMOGRAM ABNORMAL ( 11 FDA reports)
RENAL IMPAIRMENT ( 11 FDA reports)
RESTLESS LEGS SYNDROME ( 11 FDA reports)
SKIN DISORDER ( 11 FDA reports)
SPINAL FUSION SURGERY ( 11 FDA reports)
THROMBOPHLEBITIS ( 11 FDA reports)
TOXICITY TO VARIOUS AGENTS ( 11 FDA reports)
ADENOCARCINOMA ( 10 FDA reports)
APPENDICITIS ( 10 FDA reports)
BALANCE DISORDER ( 10 FDA reports)
BIPOLAR I DISORDER ( 10 FDA reports)
BONE LESION ( 10 FDA reports)
BREAST PAIN ( 10 FDA reports)
CARPAL TUNNEL SYNDROME ( 10 FDA reports)
DENTAL IMPLANTATION ( 10 FDA reports)
DIAPHRAGMATIC HERNIA ( 10 FDA reports)
DRUG DOSE OMISSION ( 10 FDA reports)
DRUG HYPERSENSITIVITY ( 10 FDA reports)
ESCHERICHIA INFECTION ( 10 FDA reports)
FACIAL BONES FRACTURE ( 10 FDA reports)
FOOT DEFORMITY ( 10 FDA reports)
GALLBLADDER POLYP ( 10 FDA reports)
HIATUS HERNIA ( 10 FDA reports)
HIP FRACTURE ( 10 FDA reports)
HYPOACUSIS ( 10 FDA reports)
HYPOPHAGIA ( 10 FDA reports)
IMPAIRED GASTRIC EMPTYING ( 10 FDA reports)
INJECTION SITE HAEMATOMA ( 10 FDA reports)
JAUNDICE ( 10 FDA reports)
MASTICATION DISORDER ( 10 FDA reports)
METASTASES TO SPINE ( 10 FDA reports)
METATARSUS PRIMUS VARUS ( 10 FDA reports)
MOUTH ULCERATION ( 10 FDA reports)
OEDEMA ( 10 FDA reports)
PALMAR-PLANTAR ERYTHRODYSAESTHESIA SYNDROME ( 10 FDA reports)
PEPTIC ULCER ( 10 FDA reports)
PERIODONTITIS ( 10 FDA reports)
PHLEBITIS ( 10 FDA reports)
RENAL ATROPHY ( 10 FDA reports)
SKIN ULCER ( 10 FDA reports)
SNORING ( 10 FDA reports)
ULCER ( 10 FDA reports)
ACQUIRED DIAPHRAGMATIC EVENTRATION ( 9 FDA reports)
ACUTE MYELOID LEUKAEMIA ( 9 FDA reports)
BLOOD LACTATE DEHYDROGENASE INCREASED ( 9 FDA reports)
CATARACT NUCLEAR ( 9 FDA reports)
CHEST DISCOMFORT ( 9 FDA reports)
CHOLELITHIASIS ( 9 FDA reports)
CONTUSION ( 9 FDA reports)
CORNEAL DYSTROPHY ( 9 FDA reports)
DENTAL CARE ( 9 FDA reports)
DERMATITIS ( 9 FDA reports)
DISABILITY ( 9 FDA reports)
DISTURBANCE IN ATTENTION ( 9 FDA reports)
DYSTONIA ( 9 FDA reports)
EXOSTOSIS ( 9 FDA reports)
FLATULENCE ( 9 FDA reports)
HISTOPLASMOSIS ( 9 FDA reports)
JAW DISORDER ( 9 FDA reports)
JOINT ANKYLOSIS ( 9 FDA reports)
LUMBAR RADICULOPATHY ( 9 FDA reports)
ODYNOPHAGIA ( 9 FDA reports)
PALLOR ( 9 FDA reports)
PLANTAR FASCIITIS ( 9 FDA reports)
PLEURODESIS ( 9 FDA reports)
SPLENIC LESION ( 9 FDA reports)
URTICARIA ( 9 FDA reports)
VENOUS THROMBOSIS LIMB ( 9 FDA reports)
VISUAL ACUITY REDUCED ( 9 FDA reports)
VISUAL IMPAIRMENT ( 9 FDA reports)
ADVERSE EVENT ( 8 FDA reports)
ALTERED STATE OF CONSCIOUSNESS ( 8 FDA reports)
ASTIGMATISM ( 8 FDA reports)
BLADDER PROLAPSE ( 8 FDA reports)
BLOOD TRIGLYCERIDES INCREASED ( 8 FDA reports)
CARDIOMYOPATHY ( 8 FDA reports)
CHOLESTASIS ( 8 FDA reports)
DEFAECATION URGENCY ( 8 FDA reports)
DENTAL CLEANING ( 8 FDA reports)
DENTAL OPERATION ( 8 FDA reports)
DENTURE WEARER ( 8 FDA reports)
DERMAL CYST ( 8 FDA reports)
DRUG WITHDRAWAL SYNDROME ( 8 FDA reports)
ESCHERICHIA SEPSIS ( 8 FDA reports)
FLUID OVERLOAD ( 8 FDA reports)
FLUSHING ( 8 FDA reports)
GASTRITIS ( 8 FDA reports)
GASTROINTESTINAL OBSTRUCTION ( 8 FDA reports)
GINGIVAL PAIN ( 8 FDA reports)
HALLUCINATION, VISUAL ( 8 FDA reports)
HEAD INJURY ( 8 FDA reports)
HEART RATE IRREGULAR ( 8 FDA reports)
HEPATIC FAILURE ( 8 FDA reports)
HYPERCALCAEMIA ( 8 FDA reports)
HYPOGLYCAEMIA ( 8 FDA reports)
IMMUNOGLOBULINS DECREASED ( 8 FDA reports)
INFLUENZA LIKE ILLNESS ( 8 FDA reports)
INTENTIONAL DRUG MISUSE ( 8 FDA reports)
ISCHAEMIC CARDIOMYOPATHY ( 8 FDA reports)
LIPIDS INCREASED ( 8 FDA reports)
METASTASES TO ABDOMINAL CAVITY ( 8 FDA reports)
MULTI-ORGAN FAILURE ( 8 FDA reports)
OESTROGEN RECEPTOR ASSAY POSITIVE ( 8 FDA reports)
ONYCHOMYCOSIS ( 8 FDA reports)
ORAL HERPES ( 8 FDA reports)
OVARIAN CYST ( 8 FDA reports)
PRODUCTIVE COUGH ( 8 FDA reports)
PYURIA ( 8 FDA reports)
STOMATITIS ( 8 FDA reports)
SWOLLEN TONGUE ( 8 FDA reports)
SYSTEMIC INFLAMMATORY RESPONSE SYNDROME ( 8 FDA reports)
THORACOTOMY ( 8 FDA reports)
THYROID NEOPLASM ( 8 FDA reports)
URINARY RETENTION ( 8 FDA reports)
UROSEPSIS ( 8 FDA reports)
UTERINE HAEMORRHAGE ( 8 FDA reports)
ABSCESS JAW ( 7 FDA reports)
ALVEOLAR OSTEITIS ( 7 FDA reports)
AMNESIA ( 7 FDA reports)
ANAPHYLACTIC REACTION ( 7 FDA reports)
ANIMAL BITE ( 7 FDA reports)
AORTIC VALVE INCOMPETENCE ( 7 FDA reports)
ARRHYTHMIA ( 7 FDA reports)
ATRIAL FIBRILLATION ( 7 FDA reports)
BLOOD ALKALINE PHOSPHATASE INCREASED ( 7 FDA reports)
BLOOD PRESSURE FLUCTUATION ( 7 FDA reports)
BRADYCARDIA ( 7 FDA reports)
BUNDLE BRANCH BLOCK LEFT ( 7 FDA reports)
CEREBROVASCULAR ACCIDENT ( 7 FDA reports)
COLITIS ( 7 FDA reports)
COLON NEOPLASM ( 7 FDA reports)
DRUG ERUPTION ( 7 FDA reports)
DYSGEUSIA ( 7 FDA reports)
EPISTAXIS ( 7 FDA reports)
ESSENTIAL HYPERTENSION ( 7 FDA reports)
GAMMA RADIATION THERAPY TO BRAIN ( 7 FDA reports)
GOITRE ( 7 FDA reports)
HEMIPARESIS ( 7 FDA reports)
HEPATIC ENZYME INCREASED ( 7 FDA reports)
HEPATITIS ( 7 FDA reports)
HYPERLIPIDAEMIA ( 7 FDA reports)
INGROWING NAIL ( 7 FDA reports)
INTERNATIONAL NORMALISED RATIO INCREASED ( 7 FDA reports)
LACRIMATION INCREASED ( 7 FDA reports)
LYMPHADENITIS ( 7 FDA reports)
MALNUTRITION ( 7 FDA reports)
MOBILITY DECREASED ( 7 FDA reports)
MYOPATHY ( 7 FDA reports)
OTITIS MEDIA ACUTE ( 7 FDA reports)
PANCREATIC NEOPLASM ( 7 FDA reports)
PHARYNGITIS ( 7 FDA reports)
PRURITUS GENERALISED ( 7 FDA reports)
RHEUMATOID ARTHRITIS ( 7 FDA reports)
RHINITIS ALLERGIC ( 7 FDA reports)
SINUS DISORDER ( 7 FDA reports)
SOCIAL AVOIDANT BEHAVIOUR ( 7 FDA reports)
THORACOSTOMY ( 7 FDA reports)
TRANSIENT ACANTHOLYTIC DERMATOSIS ( 7 FDA reports)
TRAUMATIC HAEMATOMA ( 7 FDA reports)
UNRESPONSIVE TO STIMULI ( 7 FDA reports)
VERTEBROPLASTY ( 7 FDA reports)
ACANTHOMA ( 6 FDA reports)
ACTINOMYCOSIS ( 6 FDA reports)
ANKLE FRACTURE ( 6 FDA reports)
AORTIC ARTERIOSCLEROSIS ( 6 FDA reports)
APLASTIC ANAEMIA ( 6 FDA reports)
ARRHYTHMIA SUPRAVENTRICULAR ( 6 FDA reports)
ASEPTIC NECROSIS BONE ( 6 FDA reports)
BAND NEUTROPHIL COUNT INCREASED ( 6 FDA reports)
BENIGN NEOPLASM OF THYROID GLAND ( 6 FDA reports)
BLOOD UREA NITROGEN/CREATININE RATIO INCREASED ( 6 FDA reports)
BLOOD URINE PRESENT ( 6 FDA reports)
BODY TEMPERATURE FLUCTUATION ( 6 FDA reports)
BONE MARROW FAILURE ( 6 FDA reports)
BREAST CANCER FEMALE ( 6 FDA reports)
C-REACTIVE PROTEIN INCREASED ( 6 FDA reports)
CARDIAC ARREST ( 6 FDA reports)
CATHETER SITE HAEMATOMA ( 6 FDA reports)
CROHN'S DISEASE ( 6 FDA reports)
CRYING ( 6 FDA reports)
CYSTITIS HAEMORRHAGIC ( 6 FDA reports)
DIABETIC FOOT ( 6 FDA reports)
DIASTOLIC DYSFUNCTION ( 6 FDA reports)
DILATATION VENTRICULAR ( 6 FDA reports)
DYSFUNCTIONAL UTERINE BLEEDING ( 6 FDA reports)
DYSPNOEA EXERTIONAL ( 6 FDA reports)
DYSTHYMIC DISORDER ( 6 FDA reports)
EAR DISORDER ( 6 FDA reports)
ECZEMA ( 6 FDA reports)
EDENTULOUS ( 6 FDA reports)
EPIGASTRIC DISCOMFORT ( 6 FDA reports)
EXTERNAL EAR DISORDER ( 6 FDA reports)
FAECES DISCOLOURED ( 6 FDA reports)
GASTRIC ULCER ( 6 FDA reports)
GASTROENTERITIS VIRAL ( 6 FDA reports)
HALLUCINATION ( 6 FDA reports)
HAND FRACTURE ( 6 FDA reports)
HEPATITIS ACUTE ( 6 FDA reports)
HYPERKERATOSIS ( 6 FDA reports)
HYPOXIA ( 6 FDA reports)
IMPAIRED DRIVING ABILITY ( 6 FDA reports)
INCREASED APPETITE ( 6 FDA reports)
INFLAMMATION ( 6 FDA reports)
INFLUENZA ( 6 FDA reports)
INTESTINAL ULCER ( 6 FDA reports)
INTRACARDIAC THROMBUS ( 6 FDA reports)
JAW FRACTURE ( 6 FDA reports)
LEUKOCYTOSIS ( 6 FDA reports)
LIVER DISORDER ( 6 FDA reports)
LOSS OF LIBIDO ( 6 FDA reports)
MACULE ( 6 FDA reports)
MENINGITIS ( 6 FDA reports)
MENTAL STATUS CHANGES ( 6 FDA reports)
MYELODYSPLASTIC SYNDROME ( 6 FDA reports)
MYOSITIS ( 6 FDA reports)
NERVOUSNESS ( 6 FDA reports)
NEUROGENIC BLADDER ( 6 FDA reports)
OCCULT BLOOD POSITIVE ( 6 FDA reports)
OESOPHAGEAL ULCER ( 6 FDA reports)
OFF LABEL USE ( 6 FDA reports)
OSTEOLYSIS ( 6 FDA reports)
PANCREATITIS ( 6 FDA reports)
PREAURICULAR CYST ( 6 FDA reports)
PRODUCT QUALITY ISSUE ( 6 FDA reports)
PULMONARY AIR LEAKAGE ( 6 FDA reports)
PURPURA ( 6 FDA reports)
RASH ERYTHEMATOUS ( 6 FDA reports)
RASH MACULO-PAPULAR ( 6 FDA reports)
RESPIRATORY DISTRESS ( 6 FDA reports)
RESPIRATORY FAILURE ( 6 FDA reports)
RETINAL HAEMORRHAGE ( 6 FDA reports)
SENSORY DISTURBANCE ( 6 FDA reports)
SQUAMOUS CELL CARCINOMA ( 6 FDA reports)
STRESS ( 6 FDA reports)
SUICIDE ATTEMPT ( 6 FDA reports)
SUPRAVENTRICULAR TACHYCARDIA ( 6 FDA reports)
THROMBOSIS ( 6 FDA reports)
THYROID CYST ( 6 FDA reports)
THYROID DISORDER ( 6 FDA reports)
TOOTH DISORDER ( 6 FDA reports)
WHEELCHAIR USER ( 6 FDA reports)
ABASIA ( 5 FDA reports)
ACUTE CORONARY SYNDROME ( 5 FDA reports)
AGITATION ( 5 FDA reports)
ANASTOMOTIC LEAK ( 5 FDA reports)
BACTERIAL INFECTION ( 5 FDA reports)
BLOOD ALBUMIN DECREASED ( 5 FDA reports)
CARDIOTOXICITY ( 5 FDA reports)
CENTRAL VENOUS CATHETERISATION ( 5 FDA reports)
CHOLECYSTITIS ( 5 FDA reports)
COLONIC OBSTRUCTION ( 5 FDA reports)
CONNECTIVE TISSUE DISORDER ( 5 FDA reports)
DIALYSIS ( 5 FDA reports)
DISEASE RECURRENCE ( 5 FDA reports)
DRY SKIN ( 5 FDA reports)
DYSARTHRIA ( 5 FDA reports)
EAR DISCOMFORT ( 5 FDA reports)
ENDOCARDITIS ( 5 FDA reports)
FAECALOMA ( 5 FDA reports)
GAMMA-GLUTAMYLTRANSFERASE INCREASED ( 5 FDA reports)
GASTROINTESTINAL SOUNDS ABNORMAL ( 5 FDA reports)
GLAUCOMA ( 5 FDA reports)
HAEMATOCRIT DECREASED ( 5 FDA reports)
HYPERKALAEMIA ( 5 FDA reports)
IMPAIRED WORK ABILITY ( 5 FDA reports)
IRRITABILITY ( 5 FDA reports)
LIMB DISCOMFORT ( 5 FDA reports)
LIP DRY ( 5 FDA reports)
LIP SWELLING ( 5 FDA reports)
LUNG DISORDER ( 5 FDA reports)
METRORRHAGIA ( 5 FDA reports)
MOOD ALTERED ( 5 FDA reports)
MUSCLE TWITCHING ( 5 FDA reports)
MYOCLONUS ( 5 FDA reports)
NAIL DISORDER ( 5 FDA reports)
NASAL DRYNESS ( 5 FDA reports)
PARANOIA ( 5 FDA reports)
PERFORMANCE STATUS DECREASED ( 5 FDA reports)
POST PROCEDURAL COMPLICATION ( 5 FDA reports)
RED BLOOD CELL COUNT DECREASED ( 5 FDA reports)
RENAL DISORDER ( 5 FDA reports)
ROAD TRAFFIC ACCIDENT ( 5 FDA reports)
SCAB ( 5 FDA reports)
SINUS OPERATION ( 5 FDA reports)
SKIN EXFOLIATION ( 5 FDA reports)
SPINAL COLUMN STENOSIS ( 5 FDA reports)
TOXIC NODULAR GOITRE ( 5 FDA reports)
TYPE 2 DIABETES MELLITUS ( 5 FDA reports)
URETERIC OBSTRUCTION ( 5 FDA reports)
URINE FLOW DECREASED ( 5 FDA reports)
VISUAL DISTURBANCE ( 5 FDA reports)
WOUND DEBRIDEMENT ( 5 FDA reports)
ABDOMINAL RIGIDITY ( 4 FDA reports)
ABDOMINAL TENDERNESS ( 4 FDA reports)
ACCIDENTAL OVERDOSE ( 4 FDA reports)
ACTIVITIES OF DAILY LIVING IMPAIRED ( 4 FDA reports)
ALVEOLITIS ( 4 FDA reports)
ANGER ( 4 FDA reports)
ASPIRATION ( 4 FDA reports)
ASPIRATION PLEURAL CAVITY ( 4 FDA reports)
ATELECTASIS ( 4 FDA reports)
ATRIOVENTRICULAR BLOCK COMPLETE ( 4 FDA reports)
BLINDNESS ( 4 FDA reports)
BLOOD BILIRUBIN INCREASED ( 4 FDA reports)
BONE LOSS ( 4 FDA reports)
BRAIN MASS ( 4 FDA reports)
BRONCHITIS VIRAL ( 4 FDA reports)
BUNION OPERATION ( 4 FDA reports)
CATARACT ( 4 FDA reports)
CHYLOTHORAX ( 4 FDA reports)
COGNITIVE DISORDER ( 4 FDA reports)
COLLAPSE OF LUNG ( 4 FDA reports)
COORDINATION ABNORMAL ( 4 FDA reports)
CREATININE RENAL CLEARANCE DECREASED ( 4 FDA reports)
CUSHINGOID ( 4 FDA reports)
DENTAL TREATMENT ( 4 FDA reports)
DISCOMFORT ( 4 FDA reports)
DISORIENTATION ( 4 FDA reports)
ELECTROLYTE IMBALANCE ( 4 FDA reports)
ENDODONTIC PROCEDURE ( 4 FDA reports)
EYE OEDEMA ( 4 FDA reports)
EYE PAIN ( 4 FDA reports)
FEAR ( 4 FDA reports)
FEMUR FRACTURE ( 4 FDA reports)
FIBROMYALGIA ( 4 FDA reports)
FLUID RETENTION ( 4 FDA reports)
GASTROINTESTINAL PAIN ( 4 FDA reports)
GOUT ( 4 FDA reports)
GRAFT VERSUS HOST DISEASE ( 4 FDA reports)
HEPATITIS CHOLESTATIC ( 4 FDA reports)
HEPATOTOXICITY ( 4 FDA reports)
HILAR LYMPHADENOPATHY ( 4 FDA reports)
HYDROCHOLECYSTIS ( 4 FDA reports)
HYPERURICAEMIA ( 4 FDA reports)
HYPOMAGNESAEMIA ( 4 FDA reports)
INCREASED TENDENCY TO BRUISE ( 4 FDA reports)
INITIAL INSOMNIA ( 4 FDA reports)
INJECTION SITE ERYTHEMA ( 4 FDA reports)
INJECTION SITE PAIN ( 4 FDA reports)
INTERSTITIAL LUNG DISEASE ( 4 FDA reports)
JUGULAR VEIN THROMBOSIS ( 4 FDA reports)
LIP ULCERATION ( 4 FDA reports)
LIVER INJURY ( 4 FDA reports)
LUNG INFECTION ( 4 FDA reports)
LYMPHADENOPATHY ( 4 FDA reports)
LYMPHOPENIA ( 4 FDA reports)
MEDICATION ERROR ( 4 FDA reports)
MENTAL IMPAIRMENT ( 4 FDA reports)
METASTASES TO LYMPH NODES ( 4 FDA reports)
METASTASES TO OVARY ( 4 FDA reports)
METASTASES TO PERITONEUM ( 4 FDA reports)
NASAL CONGESTION ( 4 FDA reports)
NON-SMALL CELL LUNG CANCER METASTATIC ( 4 FDA reports)
NUCLEAR MAGNETIC RESONANCE IMAGING ABNORMAL ( 4 FDA reports)
OEDEMA MUCOSAL ( 4 FDA reports)
OPTIC NEURITIS ( 4 FDA reports)
ORGASM ABNORMAL ( 4 FDA reports)
OXYGEN SATURATION DECREASED ( 4 FDA reports)
PATHOLOGICAL FRACTURE ( 4 FDA reports)
PRIMARY SEQUESTRUM ( 4 FDA reports)
PULMONARY OEDEMA ( 4 FDA reports)
PULMONARY THROMBOSIS ( 4 FDA reports)
RASH PUSTULAR ( 4 FDA reports)
RAYNAUD'S PHENOMENON ( 4 FDA reports)
RESPIRATORY DISORDER ( 4 FDA reports)
RESTRICTIVE CARDIOMYOPATHY ( 4 FDA reports)
ROTATOR CUFF SYNDROME ( 4 FDA reports)
SECRETION DISCHARGE ( 4 FDA reports)
SEROSITIS ( 4 FDA reports)
SEROTONIN SYNDROME ( 4 FDA reports)
SKIN CHAPPED ( 4 FDA reports)
SKIN TOXICITY ( 4 FDA reports)
SOPOR ( 4 FDA reports)
SPEECH DISORDER ( 4 FDA reports)
STAPHYLOCOCCAL SEPSIS ( 4 FDA reports)
STRESS FRACTURE ( 4 FDA reports)
THERAPEUTIC RESPONSE DECREASED ( 4 FDA reports)
TONGUE NEOPLASM MALIGNANT STAGE UNSPECIFIED ( 4 FDA reports)
TOOTH LOSS ( 4 FDA reports)
TROPONIN ( 4 FDA reports)
UNEVALUABLE EVENT ( 4 FDA reports)
URINARY TRACT DISORDER ( 4 FDA reports)
VAGINAL HAEMORRHAGE ( 4 FDA reports)
VERTIGO ( 4 FDA reports)
WOUND ( 4 FDA reports)
ABNORMAL BEHAVIOUR ( 3 FDA reports)
ACUTE PROMYELOCYTIC LEUKAEMIA ( 3 FDA reports)
ADNEXA UTERI MASS ( 3 FDA reports)
AGEUSIA ( 3 FDA reports)
ANTICONVULSANT DRUG LEVEL INCREASED ( 3 FDA reports)
ANTINUCLEAR ANTIBODY POSITIVE ( 3 FDA reports)
APATHY ( 3 FDA reports)
ATRIAL FLUTTER ( 3 FDA reports)
AUTOIMMUNE HEPATITIS ( 3 FDA reports)
BILIARY DILATATION ( 3 FDA reports)
BIOPSY KIDNEY ABNORMAL ( 3 FDA reports)
BLOOD CULTURE POSITIVE ( 3 FDA reports)
BLOOD POTASSIUM DECREASED ( 3 FDA reports)
BLOOD PRESSURE DECREASED ( 3 FDA reports)
BRAIN OEDEMA ( 3 FDA reports)
BREAST CANCER IN SITU ( 3 FDA reports)
BREAST MASS ( 3 FDA reports)
BREATH ODOUR ( 3 FDA reports)
BRUXISM ( 3 FDA reports)
CARDIAC TAMPONADE ( 3 FDA reports)
CAROTID ARTERY OCCLUSION ( 3 FDA reports)
CEREBRAL DISORDER ( 3 FDA reports)
CEREBRAL HAEMORRHAGE ( 3 FDA reports)
CEREBRAL INFARCTION ( 3 FDA reports)
CEREBRAL ISCHAEMIA ( 3 FDA reports)
CEREBROVASCULAR DISORDER ( 3 FDA reports)
CHOLESTATIC LIVER INJURY ( 3 FDA reports)
COMA ( 3 FDA reports)
CYSTITIS ( 3 FDA reports)
DECREASED ACTIVITY ( 3 FDA reports)
DEPRESSED LEVEL OF CONSCIOUSNESS ( 3 FDA reports)
DRUG DEPENDENCE ( 3 FDA reports)
DRUG EFFECT DECREASED ( 3 FDA reports)
DRUG LEVEL DECREASED ( 3 FDA reports)
DRUG RESISTANCE ( 3 FDA reports)
DRUG TOXICITY ( 3 FDA reports)
DRY EYE ( 3 FDA reports)
EAR HAEMORRHAGE ( 3 FDA reports)
EATING DISORDER SYMPTOM ( 3 FDA reports)
ENCEPHALITIS ( 3 FDA reports)
ENTEROCOCCAL INFECTION ( 3 FDA reports)
EXFOLIATIVE RASH ( 3 FDA reports)
FACE OEDEMA ( 3 FDA reports)
FEBRILE INFECTION ( 3 FDA reports)
FEMALE ORGASMIC DISORDER ( 3 FDA reports)
FUNGAL INFECTION ( 3 FDA reports)
GASTRIC DISORDER ( 3 FDA reports)
GASTROINTESTINAL TOXICITY ( 3 FDA reports)
GINGIVAL OPERATION ( 3 FDA reports)
HAEMARTHROSIS ( 3 FDA reports)
HAEMOPTYSIS ( 3 FDA reports)
HAEMORRHAGE INTRACRANIAL ( 3 FDA reports)
HALLUCINATION, AUDITORY ( 3 FDA reports)
HEPATIC FIBROSIS ( 3 FDA reports)
HEPATIC NECROSIS ( 3 FDA reports)
HEPATIC NEOPLASM ( 3 FDA reports)
HEPATOMEGALY ( 3 FDA reports)
HYPOCALCAEMIA ( 3 FDA reports)
IMPETIGO ( 3 FDA reports)
INFARCTION ( 3 FDA reports)
INFUSION RELATED REACTION ( 3 FDA reports)
INJECTION SITE INFLAMMATION ( 3 FDA reports)
INJECTION SITE SWELLING ( 3 FDA reports)
INJECTION SITE WARMTH ( 3 FDA reports)
INTRAOCULAR PRESSURE INCREASED ( 3 FDA reports)
IRON DEFICIENCY ANAEMIA ( 3 FDA reports)
KIDNEY ENLARGEMENT ( 3 FDA reports)
LACUNAR INFARCTION ( 3 FDA reports)
LATEX ALLERGY ( 3 FDA reports)
LEFT VENTRICULAR DYSFUNCTION ( 3 FDA reports)
LEFT VENTRICULAR HYPERTROPHY ( 3 FDA reports)
LISTLESS ( 3 FDA reports)
LOW DENSITY LIPOPROTEIN INCREASED ( 3 FDA reports)
LYMPHOCYTE COUNT DECREASED ( 3 FDA reports)
MALIGNANT PLEURAL EFFUSION ( 3 FDA reports)
MICTURITION DISORDER ( 3 FDA reports)
MUCOSAL ULCERATION ( 3 FDA reports)
MUSCULOSKELETAL DISCOMFORT ( 3 FDA reports)
MYOPIA ( 3 FDA reports)
NEPHROGENIC ANAEMIA ( 3 FDA reports)
NERVOUS SYSTEM DISORDER ( 3 FDA reports)
NEURALGIA ( 3 FDA reports)
NEUTROPENIC INFECTION ( 3 FDA reports)
NEUTROPHIL COUNT DECREASED ( 3 FDA reports)
NO THERAPEUTIC RESPONSE ( 3 FDA reports)
NORMOCHROMIC NORMOCYTIC ANAEMIA ( 3 FDA reports)
OBESITY ( 3 FDA reports)
OLIGURIA ( 3 FDA reports)
ORAL SURGERY ( 3 FDA reports)
OSTEOMYELITIS CHRONIC ( 3 FDA reports)
OTITIS EXTERNA ( 3 FDA reports)
PANCREATITIS ACUTE ( 3 FDA reports)
PANIC ATTACK ( 3 FDA reports)
PARAESTHESIA ORAL ( 3 FDA reports)
PARONYCHIA ( 3 FDA reports)
PERICARDIAL RUB ( 3 FDA reports)
PHARYNGOLARYNGEAL PAIN ( 3 FDA reports)
PRESBYOPIA ( 3 FDA reports)
PRESYNCOPE ( 3 FDA reports)
PSEUDOMONAL SEPSIS ( 3 FDA reports)
PSORIASIS ( 3 FDA reports)
PURULENCE ( 3 FDA reports)
REACTION TO DRUG EXCIPIENTS ( 3 FDA reports)
RENAL TUBULAR NECROSIS ( 3 FDA reports)
RESTLESSNESS ( 3 FDA reports)
RIGHT VENTRICULAR FAILURE ( 3 FDA reports)
SCOLIOSIS ( 3 FDA reports)
SERRATIA SEPSIS ( 3 FDA reports)
SOFT TISSUE INFECTION ( 3 FDA reports)
SPINAL FRACTURE ( 3 FDA reports)
SPINAL PAIN ( 3 FDA reports)
TARDIVE DYSKINESIA ( 3 FDA reports)
TENOSYNOVITIS ( 3 FDA reports)
THERAPEUTIC RESPONSE UNEXPECTED ( 3 FDA reports)
THROAT CANCER ( 3 FDA reports)
THROMBOCYTOSIS ( 3 FDA reports)
TOOTH REPAIR ( 3 FDA reports)
TOXIC EPIDERMAL NECROLYSIS ( 3 FDA reports)
TRANSIENT ISCHAEMIC ATTACK ( 3 FDA reports)
TREATMENT NONCOMPLIANCE ( 3 FDA reports)
TROPONIN INCREASED ( 3 FDA reports)
TYMPANIC MEMBRANE HYPERAEMIA ( 3 FDA reports)
UPPER GASTROINTESTINAL HAEMORRHAGE ( 3 FDA reports)
URINARY INCONTINENCE ( 3 FDA reports)
URINE ODOUR ABNORMAL ( 3 FDA reports)
VASCULITIS ( 3 FDA reports)
VENTRICULAR EXTRASYSTOLES ( 3 FDA reports)
VENTRICULAR HYPOKINESIA ( 3 FDA reports)
WOUND SECRETION ( 3 FDA reports)
WRONG TECHNIQUE IN DRUG USAGE PROCESS ( 3 FDA reports)
ABDOMINAL INFECTION ( 2 FDA reports)
ABDOMINAL MASS ( 2 FDA reports)
ABDOMINAL NEOPLASM ( 2 FDA reports)
ABDOMINAL PAIN LOWER ( 2 FDA reports)
ABSCESS ORAL ( 2 FDA reports)
ACANTHOSIS ( 2 FDA reports)
ACCESSORY SPLEEN ( 2 FDA reports)
ACUTE PULMONARY OEDEMA ( 2 FDA reports)
AGE-RELATED MACULAR DEGENERATION ( 2 FDA reports)
AGNOSIA ( 2 FDA reports)
ALBUMIN GLOBULIN RATIO DECREASED ( 2 FDA reports)
ANAEMIA HAEMOLYTIC AUTOIMMUNE ( 2 FDA reports)
ANOREXIA ( 2 FDA reports)
AORTIC VALVE STENOSIS ( 2 FDA reports)
APHASIA ( 2 FDA reports)
ARTERIOSCLEROSIS CORONARY ARTERY ( 2 FDA reports)
ATAXIA ( 2 FDA reports)
ATRIOVENTRICULAR BLOCK FIRST DEGREE ( 2 FDA reports)
AXILLARY PAIN ( 2 FDA reports)
BACTERAEMIA ( 2 FDA reports)
BEDRIDDEN ( 2 FDA reports)
BENIGN INTRACRANIAL HYPERTENSION ( 2 FDA reports)
BINGE EATING ( 2 FDA reports)
BIOPSY SKIN ( 2 FDA reports)
BIPOLAR DISORDER ( 2 FDA reports)
BLADDER MASS ( 2 FDA reports)
BLISTER ( 2 FDA reports)
BLOOD CALCIUM INCREASED ( 2 FDA reports)
BLOOD CHLORIDE DECREASED ( 2 FDA reports)
BLOOD CREATINE PHOSPHOKINASE MB INCREASED ( 2 FDA reports)
BODY HEIGHT DECREASED ( 2 FDA reports)
BONE DENSITY DECREASED ( 2 FDA reports)
BONE MARROW DEPRESSION ( 2 FDA reports)
BREAST CALCIFICATIONS ( 2 FDA reports)
BREAST CANCER STAGE IV ( 2 FDA reports)
BREAST INFECTION ( 2 FDA reports)
BREAST LUMP REMOVAL ( 2 FDA reports)
BREAST OPERATION ( 2 FDA reports)
BREAST SWELLING ( 2 FDA reports)
CALCIFICATION METASTATIC ( 2 FDA reports)
CARBOHYDRATE ANTIGEN 27.29 INCREASED ( 2 FDA reports)
CARBON DIOXIDE INCREASED ( 2 FDA reports)
CARDIOGENIC SHOCK ( 2 FDA reports)
CEREBELLAR HAEMORRHAGE ( 2 FDA reports)
CEREBRAL CYST ( 2 FDA reports)
CIRCULATORY COLLAPSE ( 2 FDA reports)
CLONUS ( 2 FDA reports)
COLD SWEAT ( 2 FDA reports)
COLON CANCER ( 2 FDA reports)
CONGENITAL CORONARY ARTERY MALFORMATION ( 2 FDA reports)
CONGESTIVE CARDIOMYOPATHY ( 2 FDA reports)
CORNEAL TRANSPLANT ( 2 FDA reports)
CORONARY ARTERIAL STENT INSERTION ( 2 FDA reports)
COSTOCHONDRITIS ( 2 FDA reports)
CYTOLYTIC HEPATITIS ( 2 FDA reports)
DENTAL FISTULA ( 2 FDA reports)
DIABETES MELLITUS INADEQUATE CONTROL ( 2 FDA reports)
DIABETIC RETINOPATHY ( 2 FDA reports)
DIVERTICULITIS ( 2 FDA reports)
DRUG LEVEL BELOW THERAPEUTIC ( 2 FDA reports)
DRUG LEVEL INCREASED ( 2 FDA reports)
DYSPLASIA ( 2 FDA reports)
DYSSTASIA ( 2 FDA reports)
EMBOLISM ( 2 FDA reports)
EMOTIONAL DISORDER ( 2 FDA reports)
ENCEPHALITIS HERPES ( 2 FDA reports)
ENTERITIS ( 2 FDA reports)
EOSINOPHIL COUNT DECREASED ( 2 FDA reports)
EOSINOPHILIA ( 2 FDA reports)
EPILEPSY ( 2 FDA reports)
EROSIVE OESOPHAGITIS ( 2 FDA reports)
ERUCTATION ( 2 FDA reports)
ERYTHEMA NODOSUM ( 2 FDA reports)
EYE ROLLING ( 2 FDA reports)
FAILURE OF IMPLANT ( 2 FDA reports)
FAT NECROSIS ( 2 FDA reports)
FEBRILE CONVULSION ( 2 FDA reports)
FEELING GUILTY ( 2 FDA reports)
FEELING HOT ( 2 FDA reports)
FEELING OF DESPAIR ( 2 FDA reports)
FIBRIN INCREASED ( 2 FDA reports)
FOLATE DEFICIENCY ( 2 FDA reports)
FUNGAEMIA ( 2 FDA reports)
GASTROINTESTINAL DISORDER ( 2 FDA reports)
GENERALISED OEDEMA ( 2 FDA reports)
GINGIVAL ABSCESS ( 2 FDA reports)
GINGIVAL BLEEDING ( 2 FDA reports)
GLOBULINS INCREASED ( 2 FDA reports)
GRAND MAL CONVULSION ( 2 FDA reports)
GRIP STRENGTH DECREASED ( 2 FDA reports)
GYNAECOMASTIA ( 2 FDA reports)
HAEMODIALYSIS ( 2 FDA reports)
HAIR GROWTH ABNORMAL ( 2 FDA reports)
HEARING IMPAIRED ( 2 FDA reports)
HEPATOCELLULAR INJURY ( 2 FDA reports)
HIGH DENSITY LIPOPROTEIN DECREASED ( 2 FDA reports)
HOSPITALISATION ( 2 FDA reports)
HUMERUS FRACTURE ( 2 FDA reports)
HYPERPARATHYROIDISM ( 2 FDA reports)
HYPERSOMNIA ( 2 FDA reports)
HYPERTONIA ( 2 FDA reports)
HYPERTRICHOSIS ( 2 FDA reports)
HYPOAESTHESIA ORAL ( 2 FDA reports)
HYPOALBUMINAEMIA ( 2 FDA reports)
HYPOMENORRHOEA ( 2 FDA reports)
HYPOTHYROIDISM ( 2 FDA reports)
HYPOTONIA ( 2 FDA reports)
ILEOSTOMY ( 2 FDA reports)
IMMUNODEFICIENCY ( 2 FDA reports)
INCORRECT DOSE ADMINISTERED ( 2 FDA reports)
INDURATION ( 2 FDA reports)
INFECTED CYST ( 2 FDA reports)
INJURY ASSOCIATED WITH DEVICE ( 2 FDA reports)
INTESTINAL PERFORATION ( 2 FDA reports)
INTRA-ABDOMINAL HAEMATOMA ( 2 FDA reports)
JAUNDICE CHOLESTATIC ( 2 FDA reports)
JAW OPERATION ( 2 FDA reports)
JOINT INJURY ( 2 FDA reports)
JOINT IRRIGATION ( 2 FDA reports)
LACERATION ( 2 FDA reports)
LEFT VENTRICULAR FAILURE ( 2 FDA reports)
LEUKOCYTOCLASTIC VASCULITIS ( 2 FDA reports)
LEUKODYSTROPHY ( 2 FDA reports)
LOGORRHOEA ( 2 FDA reports)
LYMPH NODE PALPABLE ( 2 FDA reports)
MACULAR DEGENERATION ( 2 FDA reports)
MALIGNANT BREAST LUMP REMOVAL ( 2 FDA reports)
MENTAL DISORDER ( 2 FDA reports)
METASTASES TO HEART ( 2 FDA reports)
METASTASES TO PLEURA ( 2 FDA reports)
MICROANGIOPATHIC HAEMOLYTIC ANAEMIA ( 2 FDA reports)
MICTURITION URGENCY ( 2 FDA reports)
MONOCYTE COUNT DECREASED ( 2 FDA reports)
MONOPLEGIA ( 2 FDA reports)
MUCOSAL INFLAMMATION ( 2 FDA reports)
MULTIPLE INJURIES ( 2 FDA reports)
MULTIPLE MYELOMA ( 2 FDA reports)
MUSCLE CRAMP ( 2 FDA reports)
MUSCLE INJURY ( 2 FDA reports)
MYELOFIBROSIS ( 2 FDA reports)
NASAL DISORDER ( 2 FDA reports)
NECK MASS ( 2 FDA reports)
NEPHRITIS INTERSTITIAL ( 2 FDA reports)
NEPHROGENIC FIBROSING DERMOPATHY ( 2 FDA reports)
NEURITIS ( 2 FDA reports)
NEUTROPHIL COUNT INCREASED ( 2 FDA reports)
NO ADVERSE EVENT ( 2 FDA reports)
NODULE ( 2 FDA reports)
NYSTAGMUS ( 2 FDA reports)
OBSTRUCTIVE AIRWAYS DISORDER ( 2 FDA reports)
ONYCHOCLASIS ( 2 FDA reports)
OPEN WOUND ( 2 FDA reports)
OPTIC ISCHAEMIC NEUROPATHY ( 2 FDA reports)
ORAL DISORDER ( 2 FDA reports)
ORAL INTAKE REDUCED ( 2 FDA reports)
ORAL SOFT TISSUE DISORDER ( 2 FDA reports)
OROANTRAL FISTULA ( 2 FDA reports)
ORTHOSTATIC HYPOTENSION ( 2 FDA reports)
OSTEOPOROTIC FRACTURE ( 2 FDA reports)
OVARIAN DISORDER ( 2 FDA reports)
PAIN OF SKIN ( 2 FDA reports)
PANCREATIC CYST ( 2 FDA reports)
PANIC REACTION ( 2 FDA reports)
PAPULE ( 2 FDA reports)
PARADOXICAL DRUG REACTION ( 2 FDA reports)
PARAKERATOSIS ( 2 FDA reports)
PERITONITIS ( 2 FDA reports)
PERIVASCULAR DERMATITIS ( 2 FDA reports)
PNEUMONIA ASPIRATION ( 2 FDA reports)
POLLAKIURIA ( 2 FDA reports)
POLYARTHRITIS ( 2 FDA reports)
POLYDIPSIA ( 2 FDA reports)
POLYNEUROPATHY TOXIC ( 2 FDA reports)
PROGRESSIVE MULTIFOCAL LEUKOENCEPHALOPATHY ( 2 FDA reports)
PULMONARY HAEMORRHAGE ( 2 FDA reports)
QUALITY OF LIFE DECREASED ( 2 FDA reports)
RADIOTHERAPY ( 2 FDA reports)
RASH GENERALISED ( 2 FDA reports)
RED BLOOD CELL SEDIMENTATION RATE INCREASED ( 2 FDA reports)
RETCHING ( 2 FDA reports)
RHINORRHOEA ( 2 FDA reports)
SARCOIDOSIS ( 2 FDA reports)
SCIATICA ( 2 FDA reports)
SCINTIGRAPHY ( 2 FDA reports)
SECONDARY HYPOGONADISM ( 2 FDA reports)
SELF ESTEEM DECREASED ( 2 FDA reports)
SELF-MEDICATION ( 2 FDA reports)
SEPTIC SHOCK ( 2 FDA reports)
SKIN DISCOLOURATION ( 2 FDA reports)
SKIN FISSURES ( 2 FDA reports)
SKIN OEDEMA ( 2 FDA reports)
SKIN REACTION ( 2 FDA reports)
STEVENS-JOHNSON SYNDROME ( 2 FDA reports)
SUBARACHNOID HAEMORRHAGE ( 2 FDA reports)
SYNCOPE VASOVAGAL ( 2 FDA reports)
THERAPY NON-RESPONDER ( 2 FDA reports)
THORACIC CAVITY DRAINAGE ( 2 FDA reports)
THROMBOCYTHAEMIA ( 2 FDA reports)
THROMBOCYTOPENIC PURPURA ( 2 FDA reports)
THROMBOTIC MICROANGIOPATHY ( 2 FDA reports)
THROMBOTIC THROMBOCYTOPENIC PURPURA ( 2 FDA reports)
TOOTH FRACTURE ( 2 FDA reports)
TOOTH INFECTION ( 2 FDA reports)
TOOTH INJURY ( 2 FDA reports)
TUBERCULIN TEST POSITIVE ( 2 FDA reports)
UPPER RESPIRATORY TRACT CONGESTION ( 2 FDA reports)
UTERINE LEIOMYOMA ( 2 FDA reports)
VERY LOW DENSITY LIPOPROTEIN INCREASED ( 2 FDA reports)
VITREOUS FLOATERS ( 2 FDA reports)
WITHDRAWAL SYNDROME ( 2 FDA reports)
WOUND DRAINAGE ( 2 FDA reports)
ABNORMAL SENSATION IN EYE ( 1 FDA reports)
ACCIDENTAL EXPOSURE ( 1 FDA reports)
ACIDOSIS ( 1 FDA reports)
ACNE ( 1 FDA reports)
ACTINOMYCOTIC SKIN INFECTION ( 1 FDA reports)
ACUTE ABDOMEN ( 1 FDA reports)
ACUTE LEUKAEMIA ( 1 FDA reports)
ACUTE PRERENAL FAILURE ( 1 FDA reports)
ACUTE RESPIRATORY DISTRESS SYNDROME ( 1 FDA reports)
ACUTE RESPIRATORY FAILURE ( 1 FDA reports)
ADRENAL INSUFFICIENCY ( 1 FDA reports)
ADVERSE REACTION ( 1 FDA reports)
AGGRESSION ( 1 FDA reports)
ALVEOLITIS ALLERGIC ( 1 FDA reports)
ANAESTHETIC COMPLICATION ( 1 FDA reports)
ANAPHYLACTOID SHOCK ( 1 FDA reports)
ANGIOEDEMA ( 1 FDA reports)
ANGIONEUROTIC OEDEMA ( 1 FDA reports)
ANGIOPLASTY ( 1 FDA reports)
ANGLE CLOSURE GLAUCOMA ( 1 FDA reports)
ANOSMIA ( 1 FDA reports)
ANOXIC ENCEPHALOPATHY ( 1 FDA reports)
ANTIBODY TEST POSITIVE ( 1 FDA reports)
AORTIC ANEURYSM ( 1 FDA reports)
AORTIC ANEURYSM RUPTURE ( 1 FDA reports)
AORTIC BRUIT ( 1 FDA reports)
AORTIC DISSECTION ( 1 FDA reports)
APHAGIA ( 1 FDA reports)
APHONIA ( 1 FDA reports)
ARTERIAL STENOSIS ( 1 FDA reports)
ARTERIOVENOUS SHUNT OPERATION ( 1 FDA reports)
ARTHRITIS REACTIVE ( 1 FDA reports)
ASTHENOPIA ( 1 FDA reports)
ATRIAL THROMBOSIS ( 1 FDA reports)
ATRIOVENTRICULAR BLOCK ( 1 FDA reports)
ATRIOVENTRICULAR BLOCK SECOND DEGREE ( 1 FDA reports)
AURA ( 1 FDA reports)
AUTOIMMUNE THYROIDITIS ( 1 FDA reports)
AXONAL NEUROPATHY ( 1 FDA reports)
AZOOSPERMIA ( 1 FDA reports)
BACTERIA BLOOD IDENTIFIED ( 1 FDA reports)
BACTERIA URINE IDENTIFIED ( 1 FDA reports)
BENIGN NEOPLASM OF EYE ( 1 FDA reports)
BILIRUBIN CONJUGATED INCREASED ( 1 FDA reports)
BIOPSY MUCOSA ABNORMAL ( 1 FDA reports)
BIOPSY SITE UNSPECIFIED ABNORMAL ( 1 FDA reports)
BITE ( 1 FDA reports)
BLADDER CANCER ( 1 FDA reports)
BLADDER PAIN ( 1 FDA reports)
BLINDNESS UNILATERAL ( 1 FDA reports)
BLOOD CHOLESTEROL ABNORMAL ( 1 FDA reports)
BLOOD FIBRINOGEN INCREASED ( 1 FDA reports)
BLOOD IRON DECREASED ( 1 FDA reports)
BLOOD PARATHYROID HORMONE INCREASED ( 1 FDA reports)
BLOOD PRESSURE SYSTOLIC INCREASED ( 1 FDA reports)
BLOOD URINE ( 1 FDA reports)
BODY TEMPERATURE INCREASED ( 1 FDA reports)
BONE CANCER METASTATIC ( 1 FDA reports)
BONE EROSION ( 1 FDA reports)
BONE MARROW DISORDER ( 1 FDA reports)
BONE NEOPLASM ( 1 FDA reports)
BONE SWELLING ( 1 FDA reports)
BREAST CANCER STAGE I ( 1 FDA reports)
BREAST DISCOLOURATION ( 1 FDA reports)
BREAST ENLARGEMENT ( 1 FDA reports)
BREAST HYPERPLASIA ( 1 FDA reports)
BREAST NECROSIS ( 1 FDA reports)
BREAST RECONSTRUCTION ( 1 FDA reports)
BREAST TENDERNESS ( 1 FDA reports)
BRONCHOALVEOLAR LAVAGE ABNORMAL ( 1 FDA reports)
CAECITIS ( 1 FDA reports)
CALCINOSIS ( 1 FDA reports)
CALCIPHYLAXIS ( 1 FDA reports)
CANDIDIASIS ( 1 FDA reports)
CARCINOMA ( 1 FDA reports)
CARDIAC FAILURE CHRONIC ( 1 FDA reports)
CARDIAC FLUTTER ( 1 FDA reports)
CARDIAC OUTPUT DECREASED ( 1 FDA reports)
CARDIOACTIVE DRUG LEVEL INCREASED ( 1 FDA reports)
CARDIOTHORACIC RATIO INCREASED ( 1 FDA reports)
CAROTID ARTERIAL EMBOLUS ( 1 FDA reports)
CAROTID ARTERY STENOSIS ( 1 FDA reports)
CAROTID BRUIT ( 1 FDA reports)
CATARACT OPERATION ( 1 FDA reports)
CATATONIA ( 1 FDA reports)
CATHETER SITE INFLAMMATION ( 1 FDA reports)
CHEMOTHERAPY ( 1 FDA reports)
CHEST TUBE INSERTION ( 1 FDA reports)
CHEST X-RAY ABNORMAL ( 1 FDA reports)
CIRCUMSTANCE OR INFORMATION CAPABLE OF LEADING TO MEDICATION ERROR ( 1 FDA reports)
CLOSTRIDIUM COLITIS ( 1 FDA reports)
CLOSTRIDIUM TEST POSITIVE ( 1 FDA reports)
COLITIS ISCHAEMIC ( 1 FDA reports)
COLITIS ULCERATIVE ( 1 FDA reports)
COMA SCALE ABNORMAL ( 1 FDA reports)
COMMUNICATION DISORDER ( 1 FDA reports)
COMPLETED SUICIDE ( 1 FDA reports)
COMPLICATIONS OF TRANSPLANTED HEART ( 1 FDA reports)
CONVERSION DISORDER ( 1 FDA reports)
CRANIOTOMY ( 1 FDA reports)
CULTURE URINE POSITIVE ( 1 FDA reports)
CUTANEOUS LUPUS ERYTHEMATOSUS ( 1 FDA reports)
CYST REMOVAL ( 1 FDA reports)
CYTOGENETIC ABNORMALITY ( 1 FDA reports)
DEAFNESS ( 1 FDA reports)
DEAFNESS BILATERAL ( 1 FDA reports)
DENTAL ALVEOLAR ANOMALY ( 1 FDA reports)
DENTAL DISCOMFORT ( 1 FDA reports)
DERMATITIS CONTACT ( 1 FDA reports)
DEVICE DIFFICULT TO USE ( 1 FDA reports)
DIABETES INSIPIDUS ( 1 FDA reports)
DIPLOPIA ( 1 FDA reports)
DISSOCIATION ( 1 FDA reports)
DISTURBANCE IN SEXUAL AROUSAL ( 1 FDA reports)
DIVERTICULAR PERFORATION ( 1 FDA reports)
DIZZINESS POSTURAL ( 1 FDA reports)
DRUG ABUSE ( 1 FDA reports)
DRUG ADMINISTRATION ERROR ( 1 FDA reports)
DRUG PRESCRIBING ERROR ( 1 FDA reports)
DRUG SCREEN FALSE POSITIVE ( 1 FDA reports)
DRUG THERAPY CHANGED ( 1 FDA reports)
DRUG TOLERANCE ( 1 FDA reports)
DRUG TOLERANCE INCREASED ( 1 FDA reports)
DUODENAL ULCER ( 1 FDA reports)
DUODENAL ULCER PERFORATION ( 1 FDA reports)
DUPUYTREN'S CONTRACTURE ( 1 FDA reports)
DYSGRAPHIA ( 1 FDA reports)
ECONOMIC PROBLEM ( 1 FDA reports)
EMBOLIC STROKE ( 1 FDA reports)
ENDOPHTHALMITIS ( 1 FDA reports)
ENDOSCOPY ( 1 FDA reports)
ENTEROCOLITIS VIRAL ( 1 FDA reports)
EPIGLOTTIC MASS ( 1 FDA reports)
ERECTILE DYSFUNCTION ( 1 FDA reports)
EUPHORIC MOOD ( 1 FDA reports)
EYE DISORDER ( 1 FDA reports)
EYE HAEMORRHAGE ( 1 FDA reports)
EYE PRURITUS ( 1 FDA reports)
EYE SWELLING ( 1 FDA reports)
EYELID FUNCTION DISORDER ( 1 FDA reports)
EYELID OEDEMA ( 1 FDA reports)
FACET JOINT SYNDROME ( 1 FDA reports)
FACIAL PALSY ( 1 FDA reports)
FAECAL INCONTINENCE ( 1 FDA reports)
FAILURE TO THRIVE ( 1 FDA reports)
FALLOPIAN TUBE DISORDER ( 1 FDA reports)
FASCIITIS ( 1 FDA reports)
FEELING COLD ( 1 FDA reports)
FEELING DRUNK ( 1 FDA reports)
FEELING JITTERY ( 1 FDA reports)
FOOD AVERSION ( 1 FDA reports)
FOREIGN BODY ( 1 FDA reports)
FRACTURE ( 1 FDA reports)
FRACTURED SACRUM ( 1 FDA reports)
FRUSTRATION ( 1 FDA reports)
GASTRECTOMY ( 1 FDA reports)
GASTRIC HAEMORRHAGE ( 1 FDA reports)
GENERAL SYMPTOM ( 1 FDA reports)
GENITAL DISORDER MALE ( 1 FDA reports)
GLOMERULONEPHRITIS ( 1 FDA reports)
GLOMERULONEPHRITIS FOCAL ( 1 FDA reports)
GLOSSITIS ( 1 FDA reports)
GLYCOSYLATED HAEMOGLOBIN INCREASED ( 1 FDA reports)
HAEMATOMA ( 1 FDA reports)
HAEMORRHOID OPERATION ( 1 FDA reports)
HALLUCINATIONS, MIXED ( 1 FDA reports)
HEART TRANSPLANT REJECTION ( 1 FDA reports)
HENOCH-SCHONLEIN PURPURA ( 1 FDA reports)
HEPARIN-INDUCED THROMBOCYTOPENIA ( 1 FDA reports)
HEPATIC ATROPHY ( 1 FDA reports)
HEPATIC LESION ( 1 FDA reports)
HEPATIC VEIN THROMBOSIS ( 1 FDA reports)
HEPATITIS C ( 1 FDA reports)
HERPES SIMPLEX ( 1 FDA reports)
HIP ARTHROPLASTY ( 1 FDA reports)
HIRSUTISM ( 1 FDA reports)
HOMOSEXUALITY ( 1 FDA reports)
HYPERADRENALISM ( 1 FDA reports)
HYPERAEMIA ( 1 FDA reports)
HYPERGAMMAGLOBULINAEMIA ( 1 FDA reports)
HYPERPHAGIA ( 1 FDA reports)
HYPERTENSIVE HEART DISEASE ( 1 FDA reports)
HYPERTHYROIDISM ( 1 FDA reports)
HYPERVIGILANCE ( 1 FDA reports)
HYPOTRICHOSIS ( 1 FDA reports)
HYPOVENTILATION ( 1 FDA reports)
IDIOPATHIC URTICARIA ( 1 FDA reports)
ILL-DEFINED DISORDER ( 1 FDA reports)
IMMUNE SYSTEM DISORDER ( 1 FDA reports)
INAPPROPRIATE ANTIDIURETIC HORMONE SECRETION ( 1 FDA reports)
INCONTINENCE ( 1 FDA reports)
INCORRECT DRUG ADMINISTRATION DURATION ( 1 FDA reports)
INCORRECT ROUTE OF DRUG ADMINISTRATION ( 1 FDA reports)
INHIBITORY DRUG INTERACTION ( 1 FDA reports)
INJECTION SITE EXTRAVASATION ( 1 FDA reports)
INJECTION SITE IRRITATION ( 1 FDA reports)
INJECTION SITE PRURITUS ( 1 FDA reports)
INJECTION SITE RASH ( 1 FDA reports)
INJECTION SITE SCAB ( 1 FDA reports)
INTENTIONAL OVERDOSE ( 1 FDA reports)
INTERVERTEBRAL DISC DISORDER ( 1 FDA reports)
INTESTINAL OBSTRUCTION ( 1 FDA reports)
INTRACRANIAL ANEURYSM ( 1 FDA reports)
JOINT CREPITATION ( 1 FDA reports)
JOINT RECONSTRUCTION ( 1 FDA reports)
JUDGEMENT IMPAIRED ( 1 FDA reports)
KLEBSIELLA INFECTION ( 1 FDA reports)
KNEE ARTHROPLASTY ( 1 FDA reports)
LABILE BLOOD PRESSURE ( 1 FDA reports)
LABILE HYPERTENSION ( 1 FDA reports)
LAPAROTOMY ( 1 FDA reports)
LARGE INTESTINAL ULCER ( 1 FDA reports)
LARYNGEAL OEDEMA ( 1 FDA reports)
LASER THERAPY ( 1 FDA reports)
LIBIDO DECREASED ( 1 FDA reports)
LICHENOID KERATOSIS ( 1 FDA reports)
LIGAMENT DISORDER ( 1 FDA reports)
LIGAMENT RUPTURE ( 1 FDA reports)
LIMB INJURY ( 1 FDA reports)
LIP AND/OR ORAL CAVITY CANCER ( 1 FDA reports)
LIP BLISTER ( 1 FDA reports)
LOCALISED OEDEMA ( 1 FDA reports)
LOW DENSITY LIPOPROTEIN DECREASED ( 1 FDA reports)
LOWER LIMB FRACTURE ( 1 FDA reports)
LOWER RESPIRATORY TRACT INFECTION ( 1 FDA reports)
LUNG INFILTRATION ( 1 FDA reports)
LUNG LOBECTOMY ( 1 FDA reports)
LUPUS-LIKE SYNDROME ( 1 FDA reports)
LYMPHADENECTOMY ( 1 FDA reports)
LYMPHANGIOSIS CARCINOMATOSA ( 1 FDA reports)
LYMPHOCYTE PERCENTAGE INCREASED ( 1 FDA reports)
LYMPHOCYTE STIMULATION TEST POSITIVE ( 1 FDA reports)
MACULAR HOLE ( 1 FDA reports)
MADAROSIS ( 1 FDA reports)
MALABSORPTION ( 1 FDA reports)
MALIGNANT HYPERTENSION ( 1 FDA reports)
MALIGNANT TUMOUR EXCISION ( 1 FDA reports)
MANDIBULECTOMY ( 1 FDA reports)
MASTECTOMY ( 1 FDA reports)
MEDIASTINOSCOPY ( 1 FDA reports)
MEDICAL DEVICE COMPLICATION ( 1 FDA reports)
MEDICATION RESIDUE ( 1 FDA reports)
MELAENA ( 1 FDA reports)
MENINGIOMA ( 1 FDA reports)
MENISCUS LESION ( 1 FDA reports)
MENOPAUSE ( 1 FDA reports)
MERYCISM ( 1 FDA reports)
METABOLIC ACIDOSIS ( 1 FDA reports)
METASTASES TO RETROPERITONEUM ( 1 FDA reports)
METASTATIC PAIN ( 1 FDA reports)
METHICILLIN-RESISTANT STAPHYLOCOCCAL AUREUS TEST POSITIVE ( 1 FDA reports)
MITRAL VALVE DISEASE ( 1 FDA reports)
MOVEMENT DISORDER ( 1 FDA reports)
MUCOSAL MEMBRANE HYPERPLASIA ( 1 FDA reports)
MULTI-ORGAN DISORDER ( 1 FDA reports)
MULTIPLE DRUG OVERDOSE ( 1 FDA reports)
MULTIPLE DRUG OVERDOSE INTENTIONAL ( 1 FDA reports)
MULTIPLE FRACTURES ( 1 FDA reports)
MUSCLE HAEMORRHAGE ( 1 FDA reports)
MUSCLE SWELLING ( 1 FDA reports)
MUSCLE TIGHTNESS ( 1 FDA reports)
MUSCULOSKELETAL DISORDER ( 1 FDA reports)
MYELOID LEUKAEMIA ( 1 FDA reports)
NAIL INFECTION ( 1 FDA reports)
NASAL SEPTUM PERFORATION ( 1 FDA reports)
NASOPHARYNGITIS ( 1 FDA reports)
NEGATIVE THOUGHTS ( 1 FDA reports)
NEOPLASM ( 1 FDA reports)
NEPHROLITHIASIS ( 1 FDA reports)
NEPHROPATHY ( 1 FDA reports)
NEPHROTIC SYNDROME ( 1 FDA reports)
NERVE COMPRESSION ( 1 FDA reports)
NEUROPATHY ( 1 FDA reports)
NEUTROPENIC SEPSIS ( 1 FDA reports)
NOCTURIA ( 1 FDA reports)
OCULAR ICTERUS ( 1 FDA reports)
OESOPHAGEAL DISORDER ( 1 FDA reports)
OESOPHAGEAL PAIN ( 1 FDA reports)
ONYCHALGIA ( 1 FDA reports)
OPTIC ATROPHY ( 1 FDA reports)
OPTIC DISC DISORDER ( 1 FDA reports)
OPTIC NEUROPATHY ( 1 FDA reports)
ORAL FUNGAL INFECTION ( 1 FDA reports)
ORGANIC ERECTILE DYSFUNCTION ( 1 FDA reports)
OSTECTOMY ( 1 FDA reports)
OSTEOMYELITIS ACUTE ( 1 FDA reports)
PAINFUL RESPIRATION ( 1 FDA reports)
PALATAL DISORDER ( 1 FDA reports)
PARANEOPLASTIC SYNDROME ( 1 FDA reports)
PELVIC DISCOMFORT ( 1 FDA reports)
PENILE PAIN ( 1 FDA reports)
PEPTIC ULCER PERFORATION ( 1 FDA reports)
PERIODONTAL DISEASE ( 1 FDA reports)
PERIPHERAL NERVE OPERATION ( 1 FDA reports)
PERIPHERAL SENSORY NEUROPATHY ( 1 FDA reports)
PERSONALITY CHANGE ( 1 FDA reports)
PHARMACEUTICAL PRODUCT COMPLAINT ( 1 FDA reports)
PHARYNGEAL OEDEMA ( 1 FDA reports)
PHOTOPSIA ( 1 FDA reports)
PITUITARY HAEMORRHAGE ( 1 FDA reports)
PLATELET COUNT INCREASED ( 1 FDA reports)
PLATELET TRANSFUSION ( 1 FDA reports)
PNEUMONIA VIRAL ( 1 FDA reports)
PNEUMONITIS ( 1 FDA reports)
PNEUMOPERITONEUM ( 1 FDA reports)
POLYP ( 1 FDA reports)
POLYPECTOMY ( 1 FDA reports)
POLYURIA ( 1 FDA reports)
POOR PERIPHERAL CIRCULATION ( 1 FDA reports)
POST GASTRIC SURGERY SYNDROME ( 1 FDA reports)
POST PROCEDURAL HAEMORRHAGE ( 1 FDA reports)
POSTERIOR REVERSIBLE ENCEPHALOPATHY SYNDROME ( 1 FDA reports)
POSTOPERATIVE INFECTION ( 1 FDA reports)
PROCTALGIA ( 1 FDA reports)
PRODUCT SIZE ISSUE ( 1 FDA reports)
PROTEIN TOTAL INCREASED ( 1 FDA reports)
PROTHROMBIN TIME PROLONGED ( 1 FDA reports)
PSEUDOMONAS INFECTION ( 1 FDA reports)
PSYCHOMOTOR HYPERACTIVITY ( 1 FDA reports)
PSYCHOTIC DISORDER ( 1 FDA reports)
PULMONARY ARTERIAL WEDGE PRESSURE INCREASED ( 1 FDA reports)
PULMONARY HYPERTENSION ( 1 FDA reports)
PULMONARY MASS ( 1 FDA reports)
PULSE ABNORMAL ( 1 FDA reports)
RADIATION PNEUMONITIS ( 1 FDA reports)
RADIATION SKIN INJURY ( 1 FDA reports)
RECTOCELE REPAIR ( 1 FDA reports)
RECURRENT CANCER ( 1 FDA reports)
REFUSAL OF TREATMENT BY PATIENT ( 1 FDA reports)
REGURGITATION ( 1 FDA reports)
RENAL COLIC ( 1 FDA reports)
RENAL FAILURE CHRONIC ( 1 FDA reports)
RESPIRATORY ARREST ( 1 FDA reports)
RESPIRATORY TRACT CONGESTION ( 1 FDA reports)
RETINAL DEGENERATION ( 1 FDA reports)
RETINITIS PIGMENTOSA ( 1 FDA reports)
RHABDOMYOLYSIS ( 1 FDA reports)
RHABDOMYOSARCOMA ( 1 FDA reports)
RIGHT VENTRICULAR DYSFUNCTION ( 1 FDA reports)
SACROILIITIS ( 1 FDA reports)
SCAR ( 1 FDA reports)
SCLERODERMA ( 1 FDA reports)
SCROTAL VARICOSE VEINS ( 1 FDA reports)
SECONDARY HYPERTENSION ( 1 FDA reports)
SENILE PRURITUS ( 1 FDA reports)
SENSATION OF HEAVINESS ( 1 FDA reports)
SEXUAL DYSFUNCTION ( 1 FDA reports)
SIALOADENITIS ( 1 FDA reports)
SICCA SYNDROME ( 1 FDA reports)
SKIN BURNING SENSATION ( 1 FDA reports)
SKIN HYPERTROPHY ( 1 FDA reports)
SKIN PAPILLOMA ( 1 FDA reports)
SKIN SENSITISATION ( 1 FDA reports)
SLEEP APNOEA SYNDROME ( 1 FDA reports)
SMALL INTESTINAL OBSTRUCTION ( 1 FDA reports)
SNEEZING ( 1 FDA reports)
SPLENIC CALCIFICATION ( 1 FDA reports)
SPLENOMEGALY ( 1 FDA reports)
STAPHYLOCOCCAL SCALDED SKIN SYNDROME ( 1 FDA reports)
STAPHYLOCOCCUS TEST POSITIVE ( 1 FDA reports)
STASIS DERMATITIS ( 1 FDA reports)
STOMACH DISCOMFORT ( 1 FDA reports)
STRABISMUS ( 1 FDA reports)
STREPTOCOCCAL SEPSIS ( 1 FDA reports)
SURGICAL PROCEDURE REPEATED ( 1 FDA reports)
SYNOVITIS ( 1 FDA reports)
SYSTEMIC LUPUS ERYTHEMATOSUS ( 1 FDA reports)
SYSTEMIC MASTOCYTOSIS ( 1 FDA reports)
TEARFULNESS ( 1 FDA reports)
TEETH BRITTLE ( 1 FDA reports)
TESTICULAR ATROPHY ( 1 FDA reports)
TESTICULAR PAIN ( 1 FDA reports)
THERAPEUTIC RESPONSE UNEXPECTED WITH DRUG SUBSTITUTION ( 1 FDA reports)
THINKING ABNORMAL ( 1 FDA reports)
THIRST ( 1 FDA reports)
THROAT IRRITATION ( 1 FDA reports)
THROAT TIGHTNESS ( 1 FDA reports)
TOBACCO USER ( 1 FDA reports)
TOBACCO WITHDRAWAL SYMPTOMS ( 1 FDA reports)
TOE OPERATION ( 1 FDA reports)
TONGUE DYSPLASIA ( 1 FDA reports)
TREATMENT RELATED SECONDARY MALIGNANCY ( 1 FDA reports)
TUBULOINTERSTITIAL NEPHRITIS ( 1 FDA reports)
UPPER LIMB FRACTURE ( 1 FDA reports)
URGE INCONTINENCE ( 1 FDA reports)
URINARY HESITATION ( 1 FDA reports)
URINE ABNORMALITY ( 1 FDA reports)
URINE COLOUR ABNORMAL ( 1 FDA reports)
URTICARIA GENERALISED ( 1 FDA reports)
UTERINE ATROPHY ( 1 FDA reports)
UTERINE PROLAPSE ( 1 FDA reports)
VASCULAR PURPURA ( 1 FDA reports)
VASOCONSTRICTION ( 1 FDA reports)
VASODILATATION ( 1 FDA reports)
VASOSPASM ( 1 FDA reports)
VENA CAVA EMBOLISM ( 1 FDA reports)
VENTRICULAR DYSFUNCTION ( 1 FDA reports)
VENTRICULAR HYPERTROPHY ( 1 FDA reports)
VENTRICULAR TACHYCARDIA ( 1 FDA reports)
VERTIGO POSITIONAL ( 1 FDA reports)
VIRAL INFECTION ( 1 FDA reports)
VITREOUS DISORDER ( 1 FDA reports)
VITREOUS HAEMORRHAGE ( 1 FDA reports)
VULVOVAGINAL DISCOMFORT ( 1 FDA reports)
WALKING AID USER ( 1 FDA reports)
WALKING DISABILITY ( 1 FDA reports)
WOUND COMPLICATION ( 1 FDA reports)
WOUND INFECTION ( 1 FDA reports)
WRIST FRACTURE ( 1 FDA reports)
X-RAY OF PELVIS AND HIP ABNORMAL ( 1 FDA reports)
XANTHOPSIA ( 1 FDA reports)
XEROSIS ( 1 FDA reports)

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