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

PAIN ( 759 FDA reports)
ANXIETY ( 665 FDA reports)
ARTHRALGIA ( 639 FDA reports)
OSTEONECROSIS OF JAW ( 609 FDA reports)
BONE DISORDER ( 591 FDA reports)
FATIGUE ( 551 FDA reports)
OSTEONECROSIS ( 522 FDA reports)
METASTASES TO BONE ( 502 FDA reports)
DYSPNOEA ( 479 FDA reports)
INJURY ( 449 FDA reports)
OSTEOARTHRITIS ( 424 FDA reports)
BACK PAIN ( 422 FDA reports)
TOOTH EXTRACTION ( 401 FDA reports)
PAIN IN JAW ( 399 FDA reports)
ASTHENIA ( 368 FDA reports)
DEPRESSION ( 367 FDA reports)
ANAEMIA ( 362 FDA reports)
OSTEOMYELITIS ( 360 FDA reports)
WEIGHT DECREASED ( 316 FDA reports)
DIZZINESS ( 312 FDA reports)
HEADACHE ( 312 FDA reports)
PLEURAL EFFUSION ( 309 FDA reports)
ANHEDONIA ( 306 FDA reports)
FALL ( 306 FDA reports)
HYPERTENSION ( 306 FDA reports)
BONE PAIN ( 304 FDA reports)
OEDEMA PERIPHERAL ( 297 FDA reports)
IMPAIRED HEALING ( 296 FDA reports)
DIARRHOEA ( 292 FDA reports)
PAIN IN EXTREMITY ( 292 FDA reports)
NAUSEA ( 286 FDA reports)
SPINAL OSTEOARTHRITIS ( 285 FDA reports)
PYREXIA ( 275 FDA reports)
HYPOAESTHESIA ( 260 FDA reports)
CHEST PAIN ( 255 FDA reports)
EMOTIONAL DISTRESS ( 253 FDA reports)
ABDOMINAL PAIN ( 252 FDA reports)
INSOMNIA ( 240 FDA reports)
CONSTIPATION ( 239 FDA reports)
INTERVERTEBRAL DISC DEGENERATION ( 236 FDA reports)
NEOPLASM MALIGNANT ( 234 FDA reports)
METASTASES TO LIVER ( 231 FDA reports)
DEATH ( 229 FDA reports)
PRIMARY SEQUESTRUM ( 228 FDA reports)
INFECTION ( 225 FDA reports)
ATELECTASIS ( 223 FDA reports)
NEUROPATHY PERIPHERAL ( 216 FDA reports)
PARAESTHESIA ( 215 FDA reports)
GASTROOESOPHAGEAL REFLUX DISEASE ( 214 FDA reports)
PNEUMONIA ( 214 FDA reports)
GAIT DISTURBANCE ( 211 FDA reports)
MALAISE ( 207 FDA reports)
OSTEOPENIA ( 206 FDA reports)
OSTEOPOROSIS ( 204 FDA reports)
TOOTH LOSS ( 202 FDA reports)
PURULENT DISCHARGE ( 197 FDA reports)
BONE LESION ( 196 FDA reports)
HEPATIC STEATOSIS ( 193 FDA reports)
INTERVERTEBRAL DISC PROTRUSION ( 190 FDA reports)
SWELLING ( 187 FDA reports)
ERYTHEMA ( 185 FDA reports)
CHRONIC OBSTRUCTIVE PULMONARY DISEASE ( 180 FDA reports)
MYALGIA ( 177 FDA reports)
LUNG NEOPLASM ( 171 FDA reports)
DECREASED APPETITE ( 170 FDA reports)
DYSPHAGIA ( 170 FDA reports)
URINARY TRACT INFECTION ( 170 FDA reports)
VOMITING ( 170 FDA reports)
BRONCHITIS ( 166 FDA reports)
DEFORMITY ( 165 FDA reports)
GENERAL PHYSICAL HEALTH DETERIORATION ( 164 FDA reports)
HOT FLUSH ( 162 FDA reports)
TOOTHACHE ( 159 FDA reports)
OSTEOSCLEROSIS ( 158 FDA reports)
RASH ( 158 FDA reports)
ALOPECIA ( 157 FDA reports)
TOOTH DISORDER ( 155 FDA reports)
METASTASES TO SPINE ( 154 FDA reports)
BONE DEBRIDEMENT ( 153 FDA reports)
COUGH ( 150 FDA reports)
BREAST CANCER ( 143 FDA reports)
HYPOKALAEMIA ( 143 FDA reports)
SYNCOPE ( 142 FDA reports)
DENTAL CARIES ( 140 FDA reports)
HYPERLIPIDAEMIA ( 140 FDA reports)
HAEMORRHOIDS ( 139 FDA reports)
MUSCULAR WEAKNESS ( 139 FDA reports)
CHOLELITHIASIS ( 138 FDA reports)
CONFUSIONAL STATE ( 135 FDA reports)
WEIGHT INCREASED ( 135 FDA reports)
ARTHRITIS ( 134 FDA reports)
MALIGNANT NEOPLASM PROGRESSION ( 134 FDA reports)
SINUSITIS ( 134 FDA reports)
OSTEITIS ( 133 FDA reports)
VISION BLURRED ( 131 FDA reports)
NECK PAIN ( 130 FDA reports)
HIATUS HERNIA ( 129 FDA reports)
PRURITUS ( 129 FDA reports)
ATRIAL FIBRILLATION ( 127 FDA reports)
DIVERTICULUM INTESTINAL ( 127 FDA reports)
SCOLIOSIS ( 127 FDA reports)
DEEP VEIN THROMBOSIS ( 125 FDA reports)
JOINT SWELLING ( 123 FDA reports)
MUSCULOSKELETAL PAIN ( 123 FDA reports)
LYMPHADENOPATHY ( 121 FDA reports)
CHRONIC SINUSITIS ( 119 FDA reports)
BREAST CANCER METASTATIC ( 116 FDA reports)
DECREASED INTEREST ( 116 FDA reports)
DEHYDRATION ( 115 FDA reports)
DYSPNOEA EXERTIONAL ( 115 FDA reports)
HYPOPHAGIA ( 114 FDA reports)
METASTASES TO LUNG ( 113 FDA reports)
CARDIAC FAILURE CONGESTIVE ( 111 FDA reports)
MUSCLE SPASMS ( 110 FDA reports)
STOMATITIS ( 109 FDA reports)
FISTULA ( 108 FDA reports)
GINGIVAL SWELLING ( 108 FDA reports)
RIB FRACTURE ( 108 FDA reports)
TOOTH FRACTURE ( 107 FDA reports)
MITRAL VALVE INCOMPETENCE ( 106 FDA reports)
PULMONARY EMBOLISM ( 106 FDA reports)
ACTINOMYCOSIS ( 105 FDA reports)
COMPRESSION FRACTURE ( 105 FDA reports)
NEOPLASM PROGRESSION ( 105 FDA reports)
NEPHROLITHIASIS ( 105 FDA reports)
SWELLING FACE ( 105 FDA reports)
ASTHMA ( 103 FDA reports)
CATARACT ( 103 FDA reports)
CELLULITIS ( 103 FDA reports)
PHYSICAL DISABILITY ( 103 FDA reports)
TOOTH INFECTION ( 103 FDA reports)
METASTASES TO CENTRAL NERVOUS SYSTEM ( 102 FDA reports)
CENTRAL VENOUS CATHETERISATION ( 101 FDA reports)
SPINAL COMPRESSION FRACTURE ( 101 FDA reports)
BURSITIS ( 100 FDA reports)
CONDITION AGGRAVATED ( 99 FDA reports)
DEBRIDEMENT ( 98 FDA reports)
SPINAL COLUMN STENOSIS ( 98 FDA reports)
TOOTH ABSCESS ( 97 FDA reports)
EXPOSED BONE IN JAW ( 96 FDA reports)
HERPES ZOSTER ( 96 FDA reports)
INFLAMMATION ( 96 FDA reports)
DISABILITY ( 95 FDA reports)
SEBORRHOEIC KERATOSIS ( 95 FDA reports)
TENDERNESS ( 95 FDA reports)
LYMPHOEDEMA ( 94 FDA reports)
BLOOD CHOLESTEROL INCREASED ( 93 FDA reports)
RENAL CYST ( 92 FDA reports)
SCAR ( 91 FDA reports)
DYSGEUSIA ( 90 FDA reports)
GASTRITIS ( 90 FDA reports)
JAW DISORDER ( 90 FDA reports)
AMNESIA ( 89 FDA reports)
CYST ( 89 FDA reports)
LOOSE TOOTH ( 88 FDA reports)
NIGHT SWEATS ( 88 FDA reports)
SEQUESTRECTOMY ( 88 FDA reports)
CARDIOMEGALY ( 87 FDA reports)
DISCOMFORT ( 87 FDA reports)
PERIODONTITIS ( 87 FDA reports)
THROMBOCYTOPENIA ( 87 FDA reports)
CHILLS ( 86 FDA reports)
DISEASE PROGRESSION ( 86 FDA reports)
EXOSTOSIS ( 86 FDA reports)
JAW OPERATION ( 86 FDA reports)
MUSCULOSKELETAL CHEST PAIN ( 86 FDA reports)
PATHOLOGICAL FRACTURE ( 86 FDA reports)
KYPHOSIS ( 85 FDA reports)
ORAL PAIN ( 85 FDA reports)
RECTAL HAEMORRHAGE ( 85 FDA reports)
EAR PAIN ( 84 FDA reports)
PALPITATIONS ( 84 FDA reports)
BLOOD ALKALINE PHOSPHATASE INCREASED ( 83 FDA reports)
CONTUSION ( 83 FDA reports)
GINGIVITIS ( 83 FDA reports)
TACHYCARDIA ( 82 FDA reports)
MASS ( 80 FDA reports)
MUSCULOSKELETAL DISCOMFORT ( 80 FDA reports)
ABDOMINAL PAIN UPPER ( 79 FDA reports)
HYPOTENSION ( 79 FDA reports)
TRANSIENT ISCHAEMIC ATTACK ( 79 FDA reports)
ARTHROPATHY ( 78 FDA reports)
BONE SCAN ABNORMAL ( 78 FDA reports)
OEDEMA ( 78 FDA reports)
TRICUSPID VALVE INCOMPETENCE ( 78 FDA reports)
DYSURIA ( 76 FDA reports)
MOUTH ULCERATION ( 76 FDA reports)
LUNG INFILTRATION ( 75 FDA reports)
OROPHARYNGEAL PAIN ( 75 FDA reports)
ABSCESS JAW ( 74 FDA reports)
BLOOD GLUCOSE INCREASED ( 74 FDA reports)
ENDODONTIC PROCEDURE ( 74 FDA reports)
MIGRAINE ( 74 FDA reports)
CENTRAL NERVOUS SYSTEM LESION ( 73 FDA reports)
LIVER FUNCTION TEST ABNORMAL ( 72 FDA reports)
NEUTROPENIA ( 72 FDA reports)
DRY MOUTH ( 71 FDA reports)
DYSPEPSIA ( 71 FDA reports)
GINGIVAL PAIN ( 71 FDA reports)
VAGINAL HAEMORRHAGE ( 71 FDA reports)
BLOOD CREATININE INCREASED ( 70 FDA reports)
ORAL CAVITY FISTULA ( 70 FDA reports)
CARPAL TUNNEL SYNDROME ( 69 FDA reports)
HYPOAESTHESIA ORAL ( 69 FDA reports)
HYPOTHYROIDISM ( 69 FDA reports)
OSTEOLYSIS ( 69 FDA reports)
URINARY INCONTINENCE ( 69 FDA reports)
ARTERIOSCLEROSIS ( 68 FDA reports)
BLOOD PRESSURE INCREASED ( 67 FDA reports)
CARDIAC MURMUR ( 67 FDA reports)
CEREBROVASCULAR ACCIDENT ( 67 FDA reports)
DENTURE WEARER ( 67 FDA reports)
DIABETES MELLITUS ( 67 FDA reports)
EXCESSIVE GRANULATION TISSUE ( 67 FDA reports)
HYPERBARIC OXYGEN THERAPY ( 67 FDA reports)
ORAL DISORDER ( 67 FDA reports)
SURGERY ( 67 FDA reports)
URTICARIA ( 67 FDA reports)
SINUS DISORDER ( 66 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 65 FDA reports)
BONE DENSITY DECREASED ( 65 FDA reports)
FEELING ABNORMAL ( 65 FDA reports)
ORAL INFECTION ( 63 FDA reports)
TENDONITIS ( 63 FDA reports)
BREATH ODOUR ( 62 FDA reports)
CORONARY ARTERY DISEASE ( 62 FDA reports)
JOINT EFFUSION ( 62 FDA reports)
SLEEP APNOEA SYNDROME ( 62 FDA reports)
ABASIA ( 61 FDA reports)
ABDOMINAL DISTENSION ( 61 FDA reports)
SYNOVIAL CYST ( 61 FDA reports)
ASCITES ( 60 FDA reports)
BONE OPERATION ( 60 FDA reports)
METASTASES TO LYMPH NODES ( 60 FDA reports)
WALKING AID USER ( 60 FDA reports)
DEVICE RELATED INFECTION ( 59 FDA reports)
DIVERTICULUM ( 59 FDA reports)
PERICARDIAL EFFUSION ( 59 FDA reports)
PLATELET COUNT DECREASED ( 59 FDA reports)
BASAL CELL CARCINOMA ( 58 FDA reports)
FEMUR FRACTURE ( 58 FDA reports)
HAEMOGLOBIN DECREASED ( 58 FDA reports)
HEPATIC LESION ( 58 FDA reports)
HYPERCHOLESTEROLAEMIA ( 58 FDA reports)
ORAL DISCOMFORT ( 58 FDA reports)
RESPIRATORY FAILURE ( 58 FDA reports)
SEPSIS ( 58 FDA reports)
ABDOMINAL DISCOMFORT ( 57 FDA reports)
DRUG INEFFECTIVE ( 57 FDA reports)
PULMONARY FIBROSIS ( 57 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 56 FDA reports)
BALANCE DISORDER ( 56 FDA reports)
CARDIAC FAILURE ( 56 FDA reports)
EATING DISORDER ( 56 FDA reports)
GINGIVAL INFECTION ( 56 FDA reports)
GINGIVAL BLEEDING ( 55 FDA reports)
HAEMATOCHEZIA ( 55 FDA reports)
HYPERKERATOSIS ( 55 FDA reports)
JAW FRACTURE ( 55 FDA reports)
LOSS OF CONSCIOUSNESS ( 55 FDA reports)
ORAL CANDIDIASIS ( 55 FDA reports)
PNEUMOTHORAX ( 55 FDA reports)
RADICULOPATHY ( 55 FDA reports)
DENTAL OPERATION ( 54 FDA reports)
HYPERHIDROSIS ( 54 FDA reports)
HYPOCALCAEMIA ( 54 FDA reports)
MEMORY IMPAIRMENT ( 54 FDA reports)
PERIODONTAL DISEASE ( 54 FDA reports)
COMPUTERISED TOMOGRAM ABNORMAL ( 53 FDA reports)
SPONDYLOLISTHESIS ( 53 FDA reports)
STAPHYLOCOCCAL INFECTION ( 53 FDA reports)
UPPER RESPIRATORY TRACT INFECTION ( 53 FDA reports)
GLAUCOMA ( 52 FDA reports)
HIP FRACTURE ( 52 FDA reports)
ORTHOSTATIC HYPOTENSION ( 52 FDA reports)
DISORIENTATION ( 51 FDA reports)
JOINT STIFFNESS ( 51 FDA reports)
PULMONARY HYPERTENSION ( 51 FDA reports)
PULMONARY MASS ( 51 FDA reports)
RENAL FAILURE CHRONIC ( 51 FDA reports)
AORTIC ARTERIOSCLEROSIS ( 50 FDA reports)
CHOLECYSTITIS ( 50 FDA reports)
FOOT FRACTURE ( 50 FDA reports)
GASTROINTESTINAL DISORDER ( 50 FDA reports)
HAEMATURIA ( 50 FDA reports)
LEUKOCYTOSIS ( 50 FDA reports)
CEREBRAL ATROPHY ( 49 FDA reports)
HYPERGLYCAEMIA ( 49 FDA reports)
MUSCULOSKELETAL STIFFNESS ( 49 FDA reports)
PANCYTOPENIA ( 49 FDA reports)
RENAL FAILURE ( 49 FDA reports)
VISUAL IMPAIRMENT ( 49 FDA reports)
BONE FRAGMENTATION ( 48 FDA reports)
GAMMA-GLUTAMYLTRANSFERASE INCREASED ( 48 FDA reports)
GLUCOSE TOLERANCE IMPAIRED ( 48 FDA reports)
GOITRE ( 48 FDA reports)
OTORRHOEA ( 48 FDA reports)
SLEEP DISORDER ( 48 FDA reports)
ACTINIC KERATOSIS ( 47 FDA reports)
DENTAL FISTULA ( 47 FDA reports)
DRY EYE ( 47 FDA reports)
IRON DEFICIENCY ANAEMIA ( 47 FDA reports)
RECTOCELE ( 47 FDA reports)
VAGINAL INFECTION ( 47 FDA reports)
VERTIGO ( 47 FDA reports)
FACET JOINT SYNDROME ( 46 FDA reports)
MENTAL STATUS CHANGES ( 46 FDA reports)
OESOPHAGITIS ( 46 FDA reports)
ORAL SURGERY ( 46 FDA reports)
RADIOTHERAPY ( 46 FDA reports)
THROMBOSIS ( 46 FDA reports)
BONE GRAFT ( 45 FDA reports)
CHEST DISCOMFORT ( 45 FDA reports)
DIPLOPIA ( 45 FDA reports)
DRUG INTERACTION ( 45 FDA reports)
FIBROSIS ( 45 FDA reports)
NEURALGIA ( 45 FDA reports)
OBESITY ( 45 FDA reports)
PALMAR-PLANTAR ERYTHRODYSAESTHESIA SYNDROME ( 45 FDA reports)
ABSCESS ORAL ( 44 FDA reports)
ACUTE SINUSITIS ( 44 FDA reports)
DEPRESSIVE SYMPTOM ( 44 FDA reports)
HAEMATOMA ( 44 FDA reports)
HEPATIC CYST ( 44 FDA reports)
HYPERCALCAEMIA ( 44 FDA reports)
INGROWING NAIL ( 44 FDA reports)
POLLAKIURIA ( 44 FDA reports)
UTERINE LEIOMYOMA ( 44 FDA reports)
WHITE BLOOD CELL COUNT DECREASED ( 44 FDA reports)
GINGIVAL DISORDER ( 43 FDA reports)
LIFE EXPECTANCY SHORTENED ( 43 FDA reports)
MYOPATHY ( 43 FDA reports)
NEURODERMATITIS ( 43 FDA reports)
ORAL MUCOSAL EXFOLIATION ( 43 FDA reports)
SUICIDAL IDEATION ( 43 FDA reports)
AGRANULOCYTOSIS ( 42 FDA reports)
GINGIVAL OEDEMA ( 42 FDA reports)
HEPATIC FUNCTION ABNORMAL ( 42 FDA reports)
VIRAL INFECTION ( 42 FDA reports)
AGITATION ( 41 FDA reports)
ALVEOLOPLASTY ( 41 FDA reports)
BLOOD CALCIUM INCREASED ( 41 FDA reports)
BONE FORMATION INCREASED ( 41 FDA reports)
DYSPHONIA ( 41 FDA reports)
PLEURAL FIBROSIS ( 41 FDA reports)
ROTATOR CUFF SYNDROME ( 41 FDA reports)
SEASONAL ALLERGY ( 41 FDA reports)
WOUND DRAINAGE ( 41 FDA reports)
ABSCESS DRAINAGE ( 40 FDA reports)
ARTIFICIAL CROWN PROCEDURE ( 40 FDA reports)
BONE SWELLING ( 40 FDA reports)
HEPATIC ENZYME INCREASED ( 40 FDA reports)
HYPERSENSITIVITY ( 40 FDA reports)
ONYCHOMYCOSIS ( 40 FDA reports)
OVARIAN CYST ( 40 FDA reports)
SOMNOLENCE ( 40 FDA reports)
URINARY RETENTION ( 40 FDA reports)
FACIAL PAIN ( 39 FDA reports)
HAEMORRHAGE ( 39 FDA reports)
HYDRONEPHROSIS ( 39 FDA reports)
LUNG DISORDER ( 39 FDA reports)
MASTICATION DISORDER ( 39 FDA reports)
RASH PRURITIC ( 39 FDA reports)
TENDON DISORDER ( 39 FDA reports)
TREMOR ( 39 FDA reports)
ANGER ( 38 FDA reports)
HEPATOMEGALY ( 38 FDA reports)
IMPLANTABLE DEFIBRILLATOR INSERTION ( 38 FDA reports)
INTERSTITIAL LUNG DISEASE ( 38 FDA reports)
PANCREATITIS ACUTE ( 38 FDA reports)
WHEEZING ( 38 FDA reports)
HUMERUS FRACTURE ( 37 FDA reports)
HYPOACUSIS ( 37 FDA reports)
INFLUENZA ( 37 FDA reports)
LOCAL SWELLING ( 37 FDA reports)
METASTATIC NEOPLASM ( 37 FDA reports)
MYOFASCIAL PAIN SYNDROME ( 37 FDA reports)
PELVIC PAIN ( 37 FDA reports)
RHINITIS ALLERGIC ( 37 FDA reports)
EYE PAIN ( 36 FDA reports)
FUNGAL INFECTION ( 36 FDA reports)
GRANULOMA ( 36 FDA reports)
LUMBAR RADICULOPATHY ( 36 FDA reports)
PARANASAL SINUS HYPERSECRETION ( 36 FDA reports)
POLYNEUROPATHY ( 36 FDA reports)
PULMONARY OEDEMA ( 36 FDA reports)
RENAL FAILURE ACUTE ( 36 FDA reports)
STOMATITIS NECROTISING ( 36 FDA reports)
BLOOD BILIRUBIN INCREASED ( 35 FDA reports)
FEBRILE NEUTROPENIA ( 35 FDA reports)
FLUID RETENTION ( 35 FDA reports)
HYPERKALAEMIA ( 35 FDA reports)
METASTATIC PAIN ( 35 FDA reports)
MITRAL VALVE PROLAPSE ( 35 FDA reports)
RESORPTION BONE INCREASED ( 35 FDA reports)
SKIN LESION ( 35 FDA reports)
TOOTH REPAIR ( 35 FDA reports)
VENOUS INSUFFICIENCY ( 35 FDA reports)
WOUND INFECTION STAPHYLOCOCCAL ( 35 FDA reports)
DENTAL CARE ( 34 FDA reports)
FAILURE TO THRIVE ( 34 FDA reports)
HEAD INJURY ( 34 FDA reports)
HYPERTROPHIC CARDIOMYOPATHY ( 34 FDA reports)
INTERVERTEBRAL DISC DISORDER ( 34 FDA reports)
INTERVERTEBRAL DISC SPACE NARROWING ( 34 FDA reports)
RENAL ATROPHY ( 34 FDA reports)
SPINAL CORD COMPRESSION ( 34 FDA reports)
BREAST CANCER RECURRENT ( 33 FDA reports)
COLONIC POLYP ( 33 FDA reports)
FACE OEDEMA ( 33 FDA reports)
FAECAL INCONTINENCE ( 33 FDA reports)
MYELOPATHY ( 33 FDA reports)
PERONEAL NERVE PALSY ( 33 FDA reports)
SMALL INTESTINAL OBSTRUCTION ( 33 FDA reports)
TINNITUS ( 33 FDA reports)
TRISMUS ( 33 FDA reports)
CARDIOMYOPATHY ( 32 FDA reports)
CYSTOCELE ( 32 FDA reports)
HAEMANGIOMA ( 32 FDA reports)
HAEMATEMESIS ( 32 FDA reports)
HEPATIC FAILURE ( 32 FDA reports)
HYPOXIA ( 32 FDA reports)
NOCTURIA ( 32 FDA reports)
ORTHOSIS USER ( 32 FDA reports)
RESTLESS LEGS SYNDROME ( 32 FDA reports)
TUMOUR MARKER INCREASED ( 32 FDA reports)
WOUND DEBRIDEMENT ( 32 FDA reports)
ABSCESS ( 31 FDA reports)
ALVEOLAR OSTEITIS ( 31 FDA reports)
ANOREXIA ( 31 FDA reports)
BIOPSY ( 31 FDA reports)
HYPOAESTHESIA FACIAL ( 31 FDA reports)
HYPOGLYCAEMIA ( 31 FDA reports)
LIVER DISORDER ( 31 FDA reports)
MALNUTRITION ( 31 FDA reports)
MYELODYSPLASTIC SYNDROME ( 31 FDA reports)
STREPTOCOCCAL INFECTION ( 31 FDA reports)
WHITE BLOOD CELL COUNT INCREASED ( 31 FDA reports)
BACTERIAL INFECTION ( 30 FDA reports)
CARDIAC DISORDER ( 30 FDA reports)
CYSTITIS ( 30 FDA reports)
GOUT ( 30 FDA reports)
NASAL MUCOSAL DISORDER ( 30 FDA reports)
SPINAL LAMINECTOMY ( 30 FDA reports)
THYROID NEOPLASM ( 30 FDA reports)
TRIGEMINAL NEURALGIA ( 30 FDA reports)
CRANIOTOMY ( 29 FDA reports)
FACE INJURY ( 29 FDA reports)
GASTROENTERITIS RADIATION ( 29 FDA reports)
GASTROINTESTINAL HAEMORRHAGE ( 29 FDA reports)
LEUKOPENIA ( 29 FDA reports)
LYMPHADENOPATHY MEDIASTINAL ( 29 FDA reports)
MACULAR DEGENERATION ( 29 FDA reports)
PARANOIA ( 29 FDA reports)
RHINORRHOEA ( 29 FDA reports)
SEROMA ( 29 FDA reports)
SINUS CONGESTION ( 29 FDA reports)
URINARY TRACT INFECTION ENTEROCOCCAL ( 29 FDA reports)
VARICOSE VEIN ( 29 FDA reports)
VITREOUS FLOATERS ( 29 FDA reports)
BLOOD TRIGLYCERIDES INCREASED ( 28 FDA reports)
CEREBRAL ISCHAEMIA ( 28 FDA reports)
COLITIS ( 28 FDA reports)
COSTOCHONDRITIS ( 28 FDA reports)
DEAFNESS ( 28 FDA reports)
DECUBITUS ULCER ( 28 FDA reports)
EYELID PTOSIS ( 28 FDA reports)
FOOT DEFORMITY ( 28 FDA reports)
FRACTURE ( 28 FDA reports)
GALLBLADDER DISORDER ( 28 FDA reports)
JOINT SPRAIN ( 28 FDA reports)
LOCALISED INFECTION ( 28 FDA reports)
MYOCARDIAL INFARCTION ( 28 FDA reports)
REFLUX OESOPHAGITIS ( 28 FDA reports)
RESPIRATORY DISORDER ( 28 FDA reports)
RHINITIS ( 28 FDA reports)
SCRATCH ( 28 FDA reports)
VOCAL CORD PARALYSIS ( 28 FDA reports)
ARTERIOSCLEROSIS CORONARY ARTERY ( 27 FDA reports)
ASPIRATION PLEURAL CAVITY ( 27 FDA reports)
BREAST CANCER FEMALE ( 27 FDA reports)
BRUXISM ( 27 FDA reports)
GROIN PAIN ( 27 FDA reports)
HEART RATE INCREASED ( 27 FDA reports)
INFLUENZA LIKE ILLNESS ( 27 FDA reports)
LARYNGEAL OEDEMA ( 27 FDA reports)
MENTAL DISORDER ( 27 FDA reports)
METAPLASIA ( 27 FDA reports)
MOUTH HAEMORRHAGE ( 27 FDA reports)
OPEN REDUCTION OF FRACTURE ( 27 FDA reports)
OVERDOSE ( 27 FDA reports)
PROTHROMBIN TIME PROLONGED ( 27 FDA reports)
SPINAL FUSION SURGERY ( 27 FDA reports)
ATROPHIC VULVOVAGINITIS ( 26 FDA reports)
BRAIN NEOPLASM ( 26 FDA reports)
COGNITIVE DISORDER ( 26 FDA reports)
DERMATITIS ( 26 FDA reports)
DRUG ABUSE ( 26 FDA reports)
HYPERTONIC BLADDER ( 26 FDA reports)
OBSTRUCTIVE AIRWAYS DISORDER ( 26 FDA reports)
PLANTAR FASCIITIS ( 26 FDA reports)
PSEUDOMONAS INFECTION ( 26 FDA reports)
SHOULDER ARTHROPLASTY ( 26 FDA reports)
SOFT TISSUE INFECTION ( 26 FDA reports)
SPINAL DISORDER ( 26 FDA reports)
THYROIDECTOMY ( 26 FDA reports)
VENTRICULAR SEPTAL DEFECT REPAIR ( 26 FDA reports)
ATRIAL FLUTTER ( 25 FDA reports)
BILE DUCT STENOSIS ( 25 FDA reports)
HYSTERECTOMY ( 25 FDA reports)
LUMBAR SPINAL STENOSIS ( 25 FDA reports)
NODULE ( 25 FDA reports)
NUCLEAR MAGNETIC RESONANCE IMAGING ABNORMAL ( 25 FDA reports)
PHARYNGEAL ERYTHEMA ( 25 FDA reports)
POLYP ( 25 FDA reports)
RESTLESSNESS ( 25 FDA reports)
RETINAL HAEMORRHAGE ( 25 FDA reports)
SENSORY LOSS ( 25 FDA reports)
UTERINE HAEMORRHAGE ( 25 FDA reports)
ADENOCARCINOMA ( 24 FDA reports)
ARRHYTHMIA ( 24 FDA reports)
ASEPTIC NECROSIS BONE ( 24 FDA reports)
BURNING SENSATION ( 24 FDA reports)
CERVICAL SPINAL STENOSIS ( 24 FDA reports)
DEPRESSED MOOD ( 24 FDA reports)
ECCHYMOSIS ( 24 FDA reports)
FIBULA FRACTURE ( 24 FDA reports)
GINGIVAL ERYTHEMA ( 24 FDA reports)
GINGIVAL RECESSION ( 24 FDA reports)
LACRIMATION INCREASED ( 24 FDA reports)
MASTECTOMY ( 24 FDA reports)
NASOPHARYNGITIS ( 24 FDA reports)
OPEN WOUND ( 24 FDA reports)
POSTURE ABNORMAL ( 24 FDA reports)
PURULENCE ( 24 FDA reports)
RASH MACULAR ( 24 FDA reports)
RHEUMATOID ARTHRITIS ( 24 FDA reports)
TEMPORAL ARTERITIS ( 24 FDA reports)
TEMPOROMANDIBULAR JOINT SYNDROME ( 24 FDA reports)
THYROID CANCER ( 24 FDA reports)
TYPE 2 DIABETES MELLITUS ( 24 FDA reports)
ANKLE FRACTURE ( 23 FDA reports)
FLUID OVERLOAD ( 23 FDA reports)
GASTROINTESTINAL PAIN ( 23 FDA reports)
HEART RATE IRREGULAR ( 23 FDA reports)
HERPES SIMPLEX ( 23 FDA reports)
HYPERPLASIA ( 23 FDA reports)
LACERATION ( 23 FDA reports)
LYMPHOMA ( 23 FDA reports)
NODAL OSTEOARTHRITIS ( 23 FDA reports)
RASH MACULO-PAPULAR ( 23 FDA reports)
RETINAL TEAR ( 23 FDA reports)
SPINAL FRACTURE ( 23 FDA reports)
THROMBOPHLEBITIS ( 23 FDA reports)
VERTEBROPLASTY ( 23 FDA reports)
AREFLEXIA ( 22 FDA reports)
BLOOD LACTATE DEHYDROGENASE INCREASED ( 22 FDA reports)
BONE CYST ( 22 FDA reports)
CACHEXIA ( 22 FDA reports)
CLOSTRIDIUM DIFFICILE COLITIS ( 22 FDA reports)
CONJUNCTIVITIS ( 22 FDA reports)
CONVULSION ( 22 FDA reports)
DYSARTHRIA ( 22 FDA reports)
EYE IRRITATION ( 22 FDA reports)
HAEMANGIOMA OF LIVER ( 22 FDA reports)
HEPATIC CIRRHOSIS ( 22 FDA reports)
HYPERCOAGULATION ( 22 FDA reports)
HYPONATRAEMIA ( 22 FDA reports)
JAUNDICE ( 22 FDA reports)
LIBIDO DECREASED ( 22 FDA reports)
LUNG NEOPLASM MALIGNANT ( 22 FDA reports)
MICTURITION URGENCY ( 22 FDA reports)
NERVE BLOCK ( 22 FDA reports)
OSTEOMYELITIS CHRONIC ( 22 FDA reports)
PROCTALGIA ( 22 FDA reports)
RENAL DISORDER ( 22 FDA reports)
SINUS HEADACHE ( 22 FDA reports)
TRANSAMINASES INCREASED ( 22 FDA reports)
VENTRICULAR EXTRASYSTOLES ( 22 FDA reports)
WALKING DISABILITY ( 22 FDA reports)
BACTERAEMIA ( 21 FDA reports)
BENIGN COLONIC NEOPLASM ( 21 FDA reports)
BLADDER CANCER RECURRENT ( 21 FDA reports)
BONE MARROW FAILURE ( 21 FDA reports)
CATARACT NUCLEAR ( 21 FDA reports)
CONNECTIVE TISSUE DISORDER ( 21 FDA reports)
DEVICE FAILURE ( 21 FDA reports)
HAEMOPTYSIS ( 21 FDA reports)
HIRSUTISM ( 21 FDA reports)
METASTASES TO PLEURA ( 21 FDA reports)
MUSCLE STRAIN ( 21 FDA reports)
POSTMENOPAUSAL HAEMORRHAGE ( 21 FDA reports)
PYOGENIC GRANULOMA ( 21 FDA reports)
SKIN ULCER ( 21 FDA reports)
SOFT TISSUE DISORDER ( 21 FDA reports)
SPINAL DECOMPRESSION ( 21 FDA reports)
SPLENOMEGALY ( 21 FDA reports)
SUPRAVENTRICULAR TACHYCARDIA ( 21 FDA reports)
UTERINE PROLAPSE ( 21 FDA reports)
ABDOMINAL HERNIA ( 20 FDA reports)
ADRENAL MASS ( 20 FDA reports)
ANGINA PECTORIS ( 20 FDA reports)
AORTIC VALVE INCOMPETENCE ( 20 FDA reports)
ASPIRATION ( 20 FDA reports)
BONE LOSS ( 20 FDA reports)
CAROTID BRUIT ( 20 FDA reports)
CATHETER PLACEMENT ( 20 FDA reports)
CHOLECYSTECTOMY ( 20 FDA reports)
DUODENITIS ( 20 FDA reports)
ECZEMA ( 20 FDA reports)
EJECTION FRACTION DECREASED ( 20 FDA reports)
EMPHYSEMA ( 20 FDA reports)
HAEMATOCRIT DECREASED ( 20 FDA reports)
HEPATIC NEOPLASM MALIGNANT ( 20 FDA reports)
HYPERMETABOLISM ( 20 FDA reports)
HYPERSOMNIA ( 20 FDA reports)
LEFT VENTRICULAR DYSFUNCTION ( 20 FDA reports)
MAJOR DEPRESSION ( 20 FDA reports)
MALIGNANT PLEURAL EFFUSION ( 20 FDA reports)
MAXILLOFACIAL OPERATION ( 20 FDA reports)
METASTASIS ( 20 FDA reports)
METRORRHAGIA ( 20 FDA reports)
NASAL CONGESTION ( 20 FDA reports)
OESOPHAGEAL CANDIDIASIS ( 20 FDA reports)
PALATAL DISORDER ( 20 FDA reports)
PERIPHERAL VASCULAR DISORDER ( 20 FDA reports)
PULMONARY GRANULOMA ( 20 FDA reports)
RADIUS FRACTURE ( 20 FDA reports)
RED BLOOD CELL COUNT DECREASED ( 20 FDA reports)
SPEECH DISORDER ( 20 FDA reports)
TOOTH DEPOSIT ( 20 FDA reports)
TUBERCULOSIS ( 20 FDA reports)
VASOGENIC CEREBRAL OEDEMA ( 20 FDA reports)
VERTEBRAL FORAMINAL STENOSIS ( 20 FDA reports)
ACTIVITIES OF DAILY LIVING IMPAIRED ( 19 FDA reports)
APHTHOUS STOMATITIS ( 19 FDA reports)
BIPOLAR I DISORDER ( 19 FDA reports)
BLOOD CALCIUM DECREASED ( 19 FDA reports)
BLOOD CREATINE PHOSPHOKINASE INCREASED ( 19 FDA reports)
BONE NEOPLASM MALIGNANT ( 19 FDA reports)
BONE TRIMMING ( 19 FDA reports)
BREAST PAIN ( 19 FDA reports)
CEREBRAL INFARCTION ( 19 FDA reports)
DYSLIPIDAEMIA ( 19 FDA reports)
FACE AND MOUTH X-RAY ABNORMAL ( 19 FDA reports)
FISTULA REPAIR ( 19 FDA reports)
HYPOALBUMINAEMIA ( 19 FDA reports)
LEFT ATRIAL DILATATION ( 19 FDA reports)
LOBAR PNEUMONIA ( 19 FDA reports)
LUNG INFECTION ( 19 FDA reports)
MALIGNANT MELANOMA ( 19 FDA reports)
MENINGIOMA ( 19 FDA reports)
MENOPAUSE ( 19 FDA reports)
METASTASES TO PELVIS ( 19 FDA reports)
MOOD ALTERED ( 19 FDA reports)
NERVOUSNESS ( 19 FDA reports)
PROCEDURAL PAIN ( 19 FDA reports)
PSORIASIS ( 19 FDA reports)
RECTAL ABSCESS ( 19 FDA reports)
RECTAL FISSURE ( 19 FDA reports)
ROAD TRAFFIC ACCIDENT ( 19 FDA reports)
TOTAL LUNG CAPACITY DECREASED ( 19 FDA reports)
AORTIC VALVE SCLEROSIS ( 18 FDA reports)
BREAST MASS ( 18 FDA reports)
CANDIDIASIS ( 18 FDA reports)
CARBOHYDRATE ANTIGEN 27.29 INCREASED ( 18 FDA reports)
CATARACT OPERATION ( 18 FDA reports)
DRUG DEPENDENCE ( 18 FDA reports)
FIBROMYALGIA ( 18 FDA reports)
HEPATITIS ( 18 FDA reports)
KIDNEY INFECTION ( 18 FDA reports)
KLEBSIELLA INFECTION ( 18 FDA reports)
METASTASES TO MENINGES ( 18 FDA reports)
METASTASES TO SKIN ( 18 FDA reports)
MORGANELLA INFECTION ( 18 FDA reports)
ORAL DISCHARGE ( 18 FDA reports)
OTITIS EXTERNA ( 18 FDA reports)
PERIODONTAL OPERATION ( 18 FDA reports)
PULMONARY CONGESTION ( 18 FDA reports)
RENAL IMPAIRMENT ( 18 FDA reports)
SINUS OPERATION ( 18 FDA reports)
SKIN DISORDER ( 18 FDA reports)
TONGUE ULCERATION ( 18 FDA reports)
ACCIDENTAL OVERDOSE ( 17 FDA reports)
ANGIOEDEMA ( 17 FDA reports)
BIOPSY BONE ABNORMAL ( 17 FDA reports)
BREAST CALCIFICATIONS ( 17 FDA reports)
BREAST NECROSIS ( 17 FDA reports)
BREAST RECONSTRUCTION ( 17 FDA reports)
BULLOUS LUNG DISEASE ( 17 FDA reports)
ENTERITIS ( 17 FDA reports)
EPISTAXIS ( 17 FDA reports)
EXCORIATION ( 17 FDA reports)
ILEUS PARALYTIC ( 17 FDA reports)
KNEE ARTHROPLASTY ( 17 FDA reports)
LICHENOID KERATOSIS ( 17 FDA reports)
LIGAMENT SPRAIN ( 17 FDA reports)
LUNG HYPERINFLATION ( 17 FDA reports)
MUCOSAL INFLAMMATION ( 17 FDA reports)
MYOPIA ( 17 FDA reports)
PANCREATITIS ( 17 FDA reports)
PAPILLOMA ( 17 FDA reports)
PERIPHERAL SENSORY NEUROPATHY ( 17 FDA reports)
PERSONALITY DISORDER ( 17 FDA reports)
PRODUCTIVE COUGH ( 17 FDA reports)
PROTEINURIA ( 17 FDA reports)
SEPTIC SHOCK ( 17 FDA reports)
SQUAMOUS CELL CARCINOMA ( 17 FDA reports)
STRESS ( 17 FDA reports)
SYNOVITIS ( 17 FDA reports)
THIRST ( 17 FDA reports)
URINE ODOUR ABNORMAL ( 17 FDA reports)
UTERINE CERVICAL SQUAMOUS METAPLASIA ( 17 FDA reports)
VISUAL ACUITY REDUCED ( 17 FDA reports)
ANGIOFIBROMA ( 16 FDA reports)
BODY HEIGHT DECREASED ( 16 FDA reports)
BREAST LUMP REMOVAL ( 16 FDA reports)
BRONCHIAL HYPERREACTIVITY ( 16 FDA reports)
CARTILAGE INJURY ( 16 FDA reports)
DERMAL CYST ( 16 FDA reports)
DRY SKIN ( 16 FDA reports)
FEELING HOT ( 16 FDA reports)
FLATULENCE ( 16 FDA reports)
GLYCOSYLATED HAEMOGLOBIN INCREASED ( 16 FDA reports)
HALLUCINATION ( 16 FDA reports)
HAND FRACTURE ( 16 FDA reports)
HORNER'S SYNDROME ( 16 FDA reports)
JOINT INJURY ( 16 FDA reports)
MEDICAL DEVICE COMPLICATION ( 16 FDA reports)
MEDICAL DEVICE REMOVAL ( 16 FDA reports)
MULTIPLE INJURIES ( 16 FDA reports)
ODYNOPHAGIA ( 16 FDA reports)
PALLOR ( 16 FDA reports)
PATELLOFEMORAL PAIN SYNDROME ( 16 FDA reports)
POOR QUALITY SLEEP ( 16 FDA reports)
RETROPERITONEAL LYMPHADENOPATHY ( 16 FDA reports)
SIGMOIDITIS ( 16 FDA reports)
SKIN CANCER ( 16 FDA reports)
SKIN PAPILLOMA ( 16 FDA reports)
SLEEP TERROR ( 16 FDA reports)
SOMNAMBULISM ( 16 FDA reports)
SPINAL DEFORMITY ( 16 FDA reports)
TRANSITIONAL CELL CARCINOMA ( 16 FDA reports)
UROSEPSIS ( 16 FDA reports)
ADRENAL ADENOMA ( 15 FDA reports)
ADRENAL INSUFFICIENCY ( 15 FDA reports)
APPENDICECTOMY ( 15 FDA reports)
APPENDICITIS PERFORATED ( 15 FDA reports)
BLINDNESS TRANSIENT ( 15 FDA reports)
BLISTER ( 15 FDA reports)
BLOOD TESTOSTERONE DECREASED ( 15 FDA reports)
BREAST PROSTHESIS USER ( 15 FDA reports)
BUNDLE BRANCH BLOCK LEFT ( 15 FDA reports)
CEREBRAL ARTERY STENOSIS ( 15 FDA reports)
COLON POLYPECTOMY ( 15 FDA reports)
CROHN'S DISEASE ( 15 FDA reports)
DRUG INTOLERANCE ( 15 FDA reports)
ERECTILE DYSFUNCTION ( 15 FDA reports)
ESCHERICHIA INFECTION ( 15 FDA reports)
LACUNAR INFARCTION ( 15 FDA reports)
OSTEITIS DEFORMANS ( 15 FDA reports)
PERIOSTITIS ( 15 FDA reports)
PNEUMONITIS ( 15 FDA reports)
PROCEDURAL HYPERTENSION ( 15 FDA reports)
PROSTATE CANCER METASTATIC ( 15 FDA reports)
PROSTATE CANCER RECURRENT ( 15 FDA reports)
PROSTATIC SPECIFIC ANTIGEN INCREASED ( 15 FDA reports)
RETCHING ( 15 FDA reports)
SALPINGO-OOPHORECTOMY BILATERAL ( 15 FDA reports)
SENSITIVITY OF TEETH ( 15 FDA reports)
SERUM FERRITIN INCREASED ( 15 FDA reports)
SMEAR CERVIX ABNORMAL ( 15 FDA reports)
SWOLLEN TONGUE ( 15 FDA reports)
UTERINE CANCER ( 15 FDA reports)
WHEELCHAIR USER ( 15 FDA reports)
WOUND DEHISCENCE ( 15 FDA reports)
ANOSMIA ( 14 FDA reports)
AORTIC CALCIFICATION ( 14 FDA reports)
APICECTOMY ( 14 FDA reports)
APPENDICITIS ( 14 FDA reports)
BIOPSY BONE ( 14 FDA reports)
BLOOD PRESSURE DECREASED ( 14 FDA reports)
BLOOD PRESSURE SYSTOLIC INCREASED ( 14 FDA reports)
BLOOD UREA INCREASED ( 14 FDA reports)
BONE ATROPHY ( 14 FDA reports)
BONE MARROW OEDEMA ( 14 FDA reports)
BREAST CYST ( 14 FDA reports)
CERVIX CARCINOMA ( 14 FDA reports)
CHEST WALL OPERATION ( 14 FDA reports)
CULTURE POSITIVE ( 14 FDA reports)
DEMENTIA ( 14 FDA reports)
DIASTOLIC DYSFUNCTION ( 14 FDA reports)
GASTROSTOMY TUBE INSERTION ( 14 FDA reports)
HIP SURGERY ( 14 FDA reports)
HORDEOLUM ( 14 FDA reports)
HYPERPARATHYROIDISM ( 14 FDA reports)
HYPERTHYROIDISM ( 14 FDA reports)
HYPOKINESIA ( 14 FDA reports)
INCISIONAL DRAINAGE ( 14 FDA reports)
INFUSION RELATED REACTION ( 14 FDA reports)
INTENTIONAL DRUG MISUSE ( 14 FDA reports)
IRRITABLE BOWEL SYNDROME ( 14 FDA reports)
KERATOCONJUNCTIVITIS SICCA ( 14 FDA reports)
LEFT VENTRICULAR HYPERTROPHY ( 14 FDA reports)
LIP BLISTER ( 14 FDA reports)
MACROCYTOSIS ( 14 FDA reports)
METABOLIC ACIDOSIS ( 14 FDA reports)
MITRAL VALVE CALCIFICATION ( 14 FDA reports)
MITRAL VALVE DISEASE ( 14 FDA reports)
MONOCYTE COUNT INCREASED ( 14 FDA reports)
MOOD SWINGS ( 14 FDA reports)
NERVOUS SYSTEM DISORDER ( 14 FDA reports)
ORTHOPEDIC PROCEDURE ( 14 FDA reports)
OSTEOSYNTHESIS ( 14 FDA reports)
PANCREATIC CYST ( 14 FDA reports)
PELVI-URETERIC OBSTRUCTION ( 14 FDA reports)
PERICARDIAL DISEASE ( 14 FDA reports)
PLATELET COUNT INCREASED ( 14 FDA reports)
PNEUMONIA ASPIRATION ( 14 FDA reports)
RADIATION INJURY ( 14 FDA reports)
RADICULITIS ( 14 FDA reports)
SENSATION OF FOREIGN BODY ( 14 FDA reports)
SPINAL HAEMANGIOMA ( 14 FDA reports)
TENOSYNOVITIS STENOSANS ( 14 FDA reports)
UNRESPONSIVE TO STIMULI ( 14 FDA reports)
UPPER LIMB FRACTURE ( 14 FDA reports)
WOUND TREATMENT ( 14 FDA reports)
ACETABULUM FRACTURE ( 13 FDA reports)
ADENOMA BENIGN ( 13 FDA reports)
AGEUSIA ( 13 FDA reports)
ANAEMIA OF MALIGNANT DISEASE ( 13 FDA reports)
APHASIA ( 13 FDA reports)
BLADDER DISORDER ( 13 FDA reports)
BLADDER OPERATION ( 13 FDA reports)
BLINDNESS ( 13 FDA reports)
BRAIN NATRIURETIC PEPTIDE INCREASED ( 13 FDA reports)
BUNION ( 13 FDA reports)
CAROTID ARTERY STENOSIS ( 13 FDA reports)
CERVICAL CORD COMPRESSION ( 13 FDA reports)
CERVIX HAEMORRHAGE UTERINE ( 13 FDA reports)
COMA ( 13 FDA reports)
DENTAL IMPLANTATION ( 13 FDA reports)
ELECTROCARDIOGRAM QT PROLONGED ( 13 FDA reports)
ENDOCRINE OPHTHALMOPATHY ( 13 FDA reports)
EPICONDYLITIS ( 13 FDA reports)
EYELID OEDEMA ( 13 FDA reports)
FACIAL BONES FRACTURE ( 13 FDA reports)
FAECES DISCOLOURED ( 13 FDA reports)
GASTRIC ULCER ( 13 FDA reports)
HEPATIC MASS ( 13 FDA reports)
HEPATITIS CHOLESTATIC ( 13 FDA reports)
HIGH DENSITY LIPOPROTEIN DECREASED ( 13 FDA reports)
HILAR LYMPHADENOPATHY ( 13 FDA reports)
HYDROCEPHALUS ( 13 FDA reports)
INTRAOCULAR LENS IMPLANT ( 13 FDA reports)
ISCHAEMIA ( 13 FDA reports)
MALOCCLUSION ( 13 FDA reports)
METASTASES TO ADRENALS ( 13 FDA reports)
MULTI-ORGAN FAILURE ( 13 FDA reports)
MYOSITIS ( 13 FDA reports)
NEUTROPHIL COUNT INCREASED ( 13 FDA reports)
OESOPHAGEAL MASS ( 13 FDA reports)
OVERWEIGHT ( 13 FDA reports)
PELVIC FRACTURE ( 13 FDA reports)
PHLEBITIS ( 13 FDA reports)
PLASTIC SURGERY ( 13 FDA reports)
PROGESTERONE RECEPTOR ASSAY POSITIVE ( 13 FDA reports)
PROSTHESIS IMPLANTATION ( 13 FDA reports)
RASH ERYTHEMATOUS ( 13 FDA reports)
RECTAL POLYP ( 13 FDA reports)
SKIN INFECTION ( 13 FDA reports)
SPINAL CORPECTOMY ( 13 FDA reports)
STEVENS-JOHNSON SYNDROME ( 13 FDA reports)
SUBDURAL HAEMATOMA ( 13 FDA reports)
SUICIDE ATTEMPT ( 13 FDA reports)
SUTURE INSERTION ( 13 FDA reports)
TENDON INJURY ( 13 FDA reports)
TIC ( 13 FDA reports)
TRANSFUSION ( 13 FDA reports)
TRIGGER FINGER ( 13 FDA reports)
VASCULAR CALCIFICATION ( 13 FDA reports)
VENOUS OCCLUSION ( 13 FDA reports)
VERTEBRAL WEDGING ( 13 FDA reports)
VITAMIN D DECREASED ( 13 FDA reports)
ADNEXA UTERI CYST ( 12 FDA reports)
AORTIC VALVE STENOSIS ( 12 FDA reports)
BLADDER CATHETERISATION ( 12 FDA reports)
BLADDER DYSFUNCTION ( 12 FDA reports)
BLADDER MASS ( 12 FDA reports)
BLINDNESS UNILATERAL ( 12 FDA reports)
CAROTID BODY TUMOUR ( 12 FDA reports)
CEREBELLAR ATROPHY ( 12 FDA reports)
CHOLECYSTITIS CHRONIC ( 12 FDA reports)
CIRCULATORY COLLAPSE ( 12 FDA reports)
CYANOSIS ( 12 FDA reports)
CYST RUPTURE ( 12 FDA reports)
DEPRESSED LEVEL OF CONSCIOUSNESS ( 12 FDA reports)
DIABETES MELLITUS INADEQUATE CONTROL ( 12 FDA reports)
EMOTIONAL DISORDER ( 12 FDA reports)
EUSTACHIAN TUBE DYSFUNCTION ( 12 FDA reports)
EYE DISORDER ( 12 FDA reports)
FACIAL OPERATION ( 12 FDA reports)
FEELING COLD ( 12 FDA reports)
FIBROCYSTIC BREAST DISEASE ( 12 FDA reports)
FISTULA DISCHARGE ( 12 FDA reports)
FOLLICULITIS ( 12 FDA reports)
HAND DEFORMITY ( 12 FDA reports)
INTERVERTEBRAL DISC OPERATION ( 12 FDA reports)
KERATOMILEUSIS ( 12 FDA reports)
MELANOCYTIC NAEVUS ( 12 FDA reports)
METASTASES TO NASAL SINUSES ( 12 FDA reports)
NERVE COMPRESSION ( 12 FDA reports)
OEDEMA MOUTH ( 12 FDA reports)
PANCREATIC CALCIFICATION ( 12 FDA reports)
PHARYNGITIS ( 12 FDA reports)
PLASTIC SURGERY TO THE FACE ( 12 FDA reports)
PSEUDOMEMBRANOUS COLITIS ( 12 FDA reports)
RHABDOMYOLYSIS ( 12 FDA reports)
RHINOPLASTY ( 12 FDA reports)
SCOTOMA ( 12 FDA reports)
SINUS BRADYCARDIA ( 12 FDA reports)
SPLEEN DISORDER ( 12 FDA reports)
TONGUE NEOPLASM MALIGNANT STAGE UNSPECIFIED ( 12 FDA reports)
TRACHEOSTOMY ( 12 FDA reports)
VISUAL DISTURBANCE ( 12 FDA reports)
VULVOVAGINAL PAIN ( 12 FDA reports)
ABDOMINAL SEPSIS ( 11 FDA reports)
ABNORMAL BEHAVIOUR ( 11 FDA reports)
ANOGENITAL WARTS ( 11 FDA reports)
BEDRIDDEN ( 11 FDA reports)
BLOOD PRESSURE FLUCTUATION ( 11 FDA reports)
BONE INFARCTION ( 11 FDA reports)
BUNDLE BRANCH BLOCK RIGHT ( 11 FDA reports)
CARDIAC FLUTTER ( 11 FDA reports)
CEREBROVASCULAR DISORDER ( 11 FDA reports)
DERMATITIS CONTACT ( 11 FDA reports)
DEVICE MALFUNCTION ( 11 FDA reports)
DIFFICULTY IN WALKING ( 11 FDA reports)
DRUG HYPERSENSITIVITY ( 11 FDA reports)
DYSAESTHESIA ( 11 FDA reports)
ELECTROCARDIOGRAM ABNORMAL ( 11 FDA reports)
ENDOTRACHEAL INTUBATION ( 11 FDA reports)
ESSENTIAL HYPERTENSION ( 11 FDA reports)
FEAR ( 11 FDA reports)
FOREIGN BODY ( 11 FDA reports)
HEMIPARESIS ( 11 FDA reports)
HEPATOTOXICITY ( 11 FDA reports)
HIP ARTHROPLASTY ( 11 FDA reports)
HYPERTRIGLYCERIDAEMIA ( 11 FDA reports)
JOINT RANGE OF MOTION DECREASED ( 11 FDA reports)
LACTOSE INTOLERANCE ( 11 FDA reports)
LARYNGITIS ( 11 FDA reports)
LENTIGO ( 11 FDA reports)
LESION EXCISION ( 11 FDA reports)
LIGAMENT INJURY ( 11 FDA reports)
LOW DENSITY LIPOPROTEIN INCREASED ( 11 FDA reports)
METASTASES TO ABDOMINAL CAVITY ( 11 FDA reports)
METASTATIC RENAL CELL CARCINOMA ( 11 FDA reports)
MUMPS ( 11 FDA reports)
MUSCULOSKELETAL DISORDER ( 11 FDA reports)
NAIL DISORDER ( 11 FDA reports)
NASAL DISORDER ( 11 FDA reports)
NECK INJURY ( 11 FDA reports)
NEOPLASM ( 11 FDA reports)
NEPHRITIC SYNDROME ( 11 FDA reports)
OCULAR HYPERAEMIA ( 11 FDA reports)
OSTEORADIONECROSIS ( 11 FDA reports)
PAINFUL RESPIRATION ( 11 FDA reports)
PETECHIAE ( 11 FDA reports)
PLEURODESIS ( 11 FDA reports)
PNEUMOCEPHALUS ( 11 FDA reports)
PRESYNCOPE ( 11 FDA reports)
PRURITUS GENERALISED ( 11 FDA reports)
PYELONEPHRITIS ACUTE ( 11 FDA reports)
RADICAL MASTECTOMY ( 11 FDA reports)
RENAL TUBULAR ACIDOSIS ( 11 FDA reports)
RUBELLA ( 11 FDA reports)
SCARLET FEVER ( 11 FDA reports)
SECRETION DISCHARGE ( 11 FDA reports)
SKIN LACERATION ( 11 FDA reports)
SYSTEMIC LUPUS ERYTHEMATOSUS ( 11 FDA reports)
VENOUS THROMBOSIS LIMB ( 11 FDA reports)
X-RAY ABNORMAL ( 11 FDA reports)
ACQUIRED DIAPHRAGMATIC EVENTRATION ( 10 FDA reports)
ACROCHORDON ( 10 FDA reports)
ANEURYSM ( 10 FDA reports)
ANIMAL BITE ( 10 FDA reports)
APHAGIA ( 10 FDA reports)
ASTIGMATISM ( 10 FDA reports)
BILE DUCT CANCER ( 10 FDA reports)
BIPOLAR DISORDER ( 10 FDA reports)
BLOOD SODIUM DECREASED ( 10 FDA reports)
BLOOD URINE PRESENT ( 10 FDA reports)
BONE DEVELOPMENT ABNORMAL ( 10 FDA reports)
BREAST ABSCESS ( 10 FDA reports)
CARDIAC ARREST ( 10 FDA reports)
CAROTID ARTERY DISEASE ( 10 FDA reports)
CERUMEN IMPACTION ( 10 FDA reports)
COLITIS ISCHAEMIC ( 10 FDA reports)
CRANIAL NERVE DISORDER ( 10 FDA reports)
DENTAL NECROSIS ( 10 FDA reports)
DIARRHOEA HAEMORRHAGIC ( 10 FDA reports)
DYSPHORIA ( 10 FDA reports)
DYSPLASTIC NAEVUS ( 10 FDA reports)
ENDOMETRIAL HYPERTROPHY ( 10 FDA reports)
ERUCTATION ( 10 FDA reports)
EYE PRURITUS ( 10 FDA reports)
GLIOSIS ( 10 FDA reports)
GRANULOMATOUS LIVER DISEASE ( 10 FDA reports)
GROIN ABSCESS ( 10 FDA reports)
HEPATITIS C ( 10 FDA reports)
HYPOVOLAEMIA ( 10 FDA reports)
ILL-DEFINED DISORDER ( 10 FDA reports)
INTERNATIONAL NORMALISED RATIO INCREASED ( 10 FDA reports)
ISCHAEMIC CEREBRAL INFARCTION ( 10 FDA reports)
JOINT ARTHROPLASTY ( 10 FDA reports)
LUNG CONSOLIDATION ( 10 FDA reports)
MACROPHAGES INCREASED ( 10 FDA reports)
MELANOSIS COLI ( 10 FDA reports)
MENORRHAGIA ( 10 FDA reports)
METATARSUS PRIMUS VARUS ( 10 FDA reports)
NECROSIS ( 10 FDA reports)
OEDEMA MUCOSAL ( 10 FDA reports)
OESOPHAGEAL ULCER ( 10 FDA reports)
OOPHORECTOMY ( 10 FDA reports)
ORAL SOFT TISSUE DISORDER ( 10 FDA reports)
ORAL TORUS ( 10 FDA reports)
ORTHOPNOEA ( 10 FDA reports)
OSTECTOMY ( 10 FDA reports)
PARAESTHESIA ORAL ( 10 FDA reports)
PERIARTHRITIS ( 10 FDA reports)
PHOTOSENSITIVITY REACTION ( 10 FDA reports)
POLYARTHRITIS ( 10 FDA reports)
PROLAPSE REPAIR ( 10 FDA reports)
RALES ( 10 FDA reports)
RENAL LIPOMATOSIS ( 10 FDA reports)
RIGHT ATRIAL DILATATION ( 10 FDA reports)
ROSACEA ( 10 FDA reports)
SALPINGO-OOPHORECTOMY ( 10 FDA reports)
SCIATICA ( 10 FDA reports)
SEBORRHOEIC DERMATITIS ( 10 FDA reports)
SELF INJURIOUS BEHAVIOUR ( 10 FDA reports)
SKIN PLAQUE ( 10 FDA reports)
SNORING ( 10 FDA reports)
SPINAL CLAUDICATION ( 10 FDA reports)
STERNOTOMY ( 10 FDA reports)
TACHYARRHYTHMIA ( 10 FDA reports)
ULCERATIVE KERATITIS ( 10 FDA reports)
UTERINE PROLAPSE REPAIR ( 10 FDA reports)
WOUND INFECTION ( 10 FDA reports)
ACNE ( 9 FDA reports)
ANAL FISSURE EXCISION ( 9 FDA reports)
ANOPLASTY ( 9 FDA reports)
BACTERIAL TEST POSITIVE ( 9 FDA reports)
BLADDER TRANSITIONAL CELL CARCINOMA ( 9 FDA reports)
BODY TEMPERATURE INCREASED ( 9 FDA reports)
BRAIN OPERATION ( 9 FDA reports)
BREAST TENDERNESS ( 9 FDA reports)
BRONCHIECTASIS ( 9 FDA reports)
C-REACTIVE PROTEIN INCREASED ( 9 FDA reports)
CERVICAL DYSPLASIA ( 9 FDA reports)
CHROMATURIA ( 9 FDA reports)
CONGENITAL CYSTIC KIDNEY DISEASE ( 9 FDA reports)
CORNEAL DYSTROPHY ( 9 FDA reports)
CRYING ( 9 FDA reports)
CYST DRAINAGE ( 9 FDA reports)
DELIRIUM ( 9 FDA reports)
DUODENAL POLYP ( 9 FDA reports)
EDENTULOUS ( 9 FDA reports)
ENDOMETRIOSIS ( 9 FDA reports)
ENTEROCELE ( 9 FDA reports)
FIBROMA ( 9 FDA reports)
FLUSHING ( 9 FDA reports)
GASTRIC POLYPS ( 9 FDA reports)
GASTROENTERITIS ( 9 FDA reports)
GASTROENTERITIS CLOSTRIDIAL ( 9 FDA reports)
GLUCOSE TOLERANCE TEST ABNORMAL ( 9 FDA reports)
GRAM STAIN POSITIVE ( 9 FDA reports)
HAEMATOCRIT ABNORMAL ( 9 FDA reports)
HYDROURETER ( 9 FDA reports)
INCONTINENCE ( 9 FDA reports)
LOCALISED OEDEMA ( 9 FDA reports)
MACROGLOSSIA ( 9 FDA reports)
MONARTHRITIS ( 9 FDA reports)
MUCOSAL EROSION ( 9 FDA reports)
MYOMECTOMY ( 9 FDA reports)
OCCULT BLOOD POSITIVE ( 9 FDA reports)
OESOPHAGEAL STENOSIS ( 9 FDA reports)
ONYCHOGRYPHOSIS ( 9 FDA reports)
ORAL HERPES ( 9 FDA reports)
PERIPHERAL ARTERIAL OCCLUSIVE DISEASE ( 9 FDA reports)
PHYSIOTHERAPY ( 9 FDA reports)
PLATELET DISORDER ( 9 FDA reports)
POLYCYTHAEMIA ( 9 FDA reports)
RED BLOOD CELL ABNORMALITY ( 9 FDA reports)
RENAL CANCER ( 9 FDA reports)
SCINTIGRAPHY ( 9 FDA reports)
SENSATION OF PRESSURE ( 9 FDA reports)
SINUS TACHYCARDIA ( 9 FDA reports)
SKIN DISCOLOURATION ( 9 FDA reports)
SKIN EXFOLIATION ( 9 FDA reports)
STASIS DERMATITIS ( 9 FDA reports)
STENT PLACEMENT ( 9 FDA reports)
THORACOSTOMY ( 9 FDA reports)
THROAT CANCER ( 9 FDA reports)
TONGUE PARALYSIS ( 9 FDA reports)
TOOTH INJURY ( 9 FDA reports)
TOOTH RESORPTION ( 9 FDA reports)
ULCER ( 9 FDA reports)
ULTRASOUND PELVIS ABNORMAL ( 9 FDA reports)
URETERIC OBSTRUCTION ( 9 FDA reports)
URINE CYTOLOGY ABNORMAL ( 9 FDA reports)
URINE OUTPUT DECREASED ( 9 FDA reports)
VIITH NERVE PARALYSIS ( 9 FDA reports)
VIRAL LABYRINTHITIS ( 9 FDA reports)
VULVOVAGINAL DRYNESS ( 9 FDA reports)
WHITE BLOOD CELL DISORDER ( 9 FDA reports)
ACCELERATED HYPERTENSION ( 8 FDA reports)
ADRENAL NEOPLASM ( 8 FDA reports)
ANTINUCLEAR ANTIBODY POSITIVE ( 8 FDA reports)
AORTIC VALVE DISEASE ( 8 FDA reports)
ARTIFICIAL MENOPAUSE ( 8 FDA reports)
ATRIAL TACHYCARDIA ( 8 FDA reports)
ATRIOVENTRICULAR BLOCK ( 8 FDA reports)
ATRIOVENTRICULAR BLOCK COMPLETE ( 8 FDA reports)
AUTONOMIC NEUROPATHY ( 8 FDA reports)
BLADDER PROLAPSE ( 8 FDA reports)
BLOOD COUNT ABNORMAL ( 8 FDA reports)
BLOOD POTASSIUM DECREASED ( 8 FDA reports)
BREAST ENLARGEMENT ( 8 FDA reports)
CARCINOEMBRYONIC ANTIGEN INCREASED ( 8 FDA reports)
CHEMOTHERAPY ( 8 FDA reports)
COLONOSCOPY ABNORMAL ( 8 FDA reports)
CONTRALATERAL BREAST CANCER ( 8 FDA reports)
CREPITATIONS ( 8 FDA reports)
DEAFNESS NEUROSENSORY ( 8 FDA reports)
DENTAL PROSTHESIS PLACEMENT ( 8 FDA reports)
DENTAL TREATMENT ( 8 FDA reports)
DISEASE RECURRENCE ( 8 FDA reports)
DISTURBANCE IN ATTENTION ( 8 FDA reports)
DIVERTICULITIS ( 8 FDA reports)
DYSPHEMIA ( 8 FDA reports)
DYSTHYMIC DISORDER ( 8 FDA reports)
EAR DISCOMFORT ( 8 FDA reports)
ECONOMIC PROBLEM ( 8 FDA reports)
EMBOLISM ( 8 FDA reports)
EROSIVE OESOPHAGITIS ( 8 FDA reports)
ERYTHEMA MULTIFORME ( 8 FDA reports)
FOOT OPERATION ( 8 FDA reports)
GINGIVAL ABSCESS ( 8 FDA reports)
GINGIVAL ULCERATION ( 8 FDA reports)
GRAND MAL CONVULSION ( 8 FDA reports)
HEART RATE DECREASED ( 8 FDA reports)
HELICOBACTER GASTRITIS ( 8 FDA reports)
HEPATIC NEOPLASM ( 8 FDA reports)
HEPATOCELLULAR DAMAGE ( 8 FDA reports)
HYPERALBUMINAEMIA ( 8 FDA reports)
HYPERTRANSAMINASAEMIA ( 8 FDA reports)
HYPOMAGNESAEMIA ( 8 FDA reports)
ISCHAEMIC STROKE ( 8 FDA reports)
JOINT DISLOCATION ( 8 FDA reports)
KYPHOSCOLIOSIS ( 8 FDA reports)
LIMB DISCOMFORT ( 8 FDA reports)
LUNG CANCER METASTATIC ( 8 FDA reports)
LYMPHADENECTOMY ( 8 FDA reports)
LYMPHANGIOSIS CARCINOMATOSA ( 8 FDA reports)
LYMPHOCYTE COUNT DECREASED ( 8 FDA reports)
MAMMOPLASTY ( 8 FDA reports)
METABOLIC SYNDROME ( 8 FDA reports)
METASTASES TO BONE MARROW ( 8 FDA reports)
METASTASES TO EYE ( 8 FDA reports)
METASTASES TO HEART ( 8 FDA reports)
METASTASES TO STOMACH ( 8 FDA reports)
MUCOSAL ULCERATION ( 8 FDA reports)
NAIL OPERATION ( 8 FDA reports)
NEOPLASM SKIN ( 8 FDA reports)
NO ADVERSE EVENT ( 8 FDA reports)
OESTROGEN RECEPTOR ASSAY POSITIVE ( 8 FDA reports)
OPTIC NEUROPATHY ( 8 FDA reports)
OROANTRAL FISTULA ( 8 FDA reports)
OTITIS MEDIA ACUTE ( 8 FDA reports)
OXYGEN SATURATION DECREASED ( 8 FDA reports)
PANIC ATTACK ( 8 FDA reports)
PERIODONTAL INFECTION ( 8 FDA reports)
PHAEOCHROMOCYTOMA ( 8 FDA reports)
PHOTODERMATOSIS ( 8 FDA reports)
PHOTOPHOBIA ( 8 FDA reports)
POST PROCEDURAL COMPLICATION ( 8 FDA reports)
PROCTITIS ( 8 FDA reports)
PYURIA ( 8 FDA reports)
RED CELL DISTRIBUTION WIDTH INCREASED ( 8 FDA reports)
REGURGITATION ( 8 FDA reports)
RESPIRATORY DISTRESS ( 8 FDA reports)
RESPIRATORY TRACT CONGESTION ( 8 FDA reports)
RETINAL DETACHMENT ( 8 FDA reports)
RIB DEFORMITY ( 8 FDA reports)
RIGHT VENTRICULAR FAILURE ( 8 FDA reports)
SALIVARY HYPERSECRETION ( 8 FDA reports)
SENSATION OF HEAVINESS ( 8 FDA reports)
SEROSITIS ( 8 FDA reports)
SINGLE FUNCTIONAL KIDNEY ( 8 FDA reports)
SINUS ARRHYTHMIA ( 8 FDA reports)
SKIN REACTION ( 8 FDA reports)
VASOMOTOR RHINITIS ( 8 FDA reports)
VENA CAVA INJURY ( 8 FDA reports)
VENTRICULAR HYPERTROPHY ( 8 FDA reports)
VITAMIN B12 DEFICIENCY ( 8 FDA reports)
WOUND ( 8 FDA reports)
XANTHOGRANULOMA ( 8 FDA reports)
ABDOMINAL PAIN LOWER ( 7 FDA reports)
ACUTE MYELOID LEUKAEMIA ( 7 FDA reports)
AGGRESSION ( 7 FDA reports)
ANGIOPATHY ( 7 FDA reports)
AORTIC ANEURYSM ( 7 FDA reports)
APICAL GRANULOMA ( 7 FDA reports)
ARRHYTHMIA SUPRAVENTRICULAR ( 7 FDA reports)
AXILLARY MASS ( 7 FDA reports)
BILE DUCT OBSTRUCTION ( 7 FDA reports)
BILIARY DILATATION ( 7 FDA reports)
BONE CALLUS EXCESSIVE ( 7 FDA reports)
BREAST CANCER STAGE I ( 7 FDA reports)
CARDIAC PACEMAKER INSERTION ( 7 FDA reports)
CEREBRAL ARTERIOSCLEROSIS ( 7 FDA reports)
CHEST TUBE INSERTION ( 7 FDA reports)
CHOLESTASIS ( 7 FDA reports)
CYTOLYTIC HEPATITIS ( 7 FDA reports)
DIALYSIS ( 7 FDA reports)
DYSFUNCTIONAL UTERINE BLEEDING ( 7 FDA reports)
EFFUSION ( 7 FDA reports)
ENCEPHALOMALACIA ( 7 FDA reports)
ENDOMETRIAL DISORDER ( 7 FDA reports)
ETHMOID SINUS SURGERY ( 7 FDA reports)
GAMMA-GLUTAMYLTRANSFERASE DECREASED ( 7 FDA reports)
GASTROINTESTINAL OBSTRUCTION ( 7 FDA reports)
GASTROINTESTINAL TOXICITY ( 7 FDA reports)
GLOSSODYNIA ( 7 FDA reports)
HAIR GROWTH ABNORMAL ( 7 FDA reports)
HEPATIC FIBROSIS ( 7 FDA reports)
HYPERTENSIVE HEART DISEASE ( 7 FDA reports)
IMPAIRED DRIVING ABILITY ( 7 FDA reports)
LETHARGY ( 7 FDA reports)
LICHEN PLANUS ( 7 FDA reports)
LIPOMA ( 7 FDA reports)
LYMPHADENITIS ( 7 FDA reports)
MALIGNANT BREAST LUMP REMOVAL ( 7 FDA reports)
MOBILITY DECREASED ( 7 FDA reports)
MULTIPLE SCLEROSIS ( 7 FDA reports)
NASAL DISCOMFORT ( 7 FDA reports)
NASAL SEPTUM DEVIATION ( 7 FDA reports)
ORAL FUNGAL INFECTION ( 7 FDA reports)
ORAL PAPILLOMA ( 7 FDA reports)
OVARIAN CANCER ( 7 FDA reports)
PAIN OF SKIN ( 7 FDA reports)
PARALYSIS ( 7 FDA reports)
PARKINSONISM ( 7 FDA reports)
PEPTIC ULCER ( 7 FDA reports)
PERCUSSION TEST ABNORMAL ( 7 FDA reports)
PITUITARY TUMOUR BENIGN ( 7 FDA reports)
POST PROCEDURAL DISCHARGE ( 7 FDA reports)
PRODUCT QUALITY ISSUE ( 7 FDA reports)
PULMONARY HILUM MASS ( 7 FDA reports)
RADICULAR PAIN ( 7 FDA reports)
RECURRENT CANCER ( 7 FDA reports)
RESIDUAL URINE ( 7 FDA reports)
RESIDUAL URINE VOLUME ( 7 FDA reports)
SARCOIDOSIS ( 7 FDA reports)
SINUS ANTROSTOMY ( 7 FDA reports)
SKELETAL INJURY ( 7 FDA reports)
STAPHYLOCOCCAL SEPSIS ( 7 FDA reports)
SUBCLAVIAN VEIN THROMBOSIS ( 7 FDA reports)
THERAPY NON-RESPONDER ( 7 FDA reports)
THORACIC VERTEBRAL FRACTURE ( 7 FDA reports)
TONSILLAR DISORDER ( 7 FDA reports)
TRACHEO-OESOPHAGEAL FISTULA ( 7 FDA reports)
UNEVALUABLE EVENT ( 7 FDA reports)
VARICES OESOPHAGEAL ( 7 FDA reports)
VULVOVAGINAL CANDIDIASIS ( 7 FDA reports)
ADRENAL CARCINOMA ( 6 FDA reports)
ALLERGIC SINUSITIS ( 6 FDA reports)
AMAUROSIS FUGAX ( 6 FDA reports)
ANGINA UNSTABLE ( 6 FDA reports)
APHONIA ( 6 FDA reports)
APPETITE DISORDER ( 6 FDA reports)
AZOTAEMIA ( 6 FDA reports)
BACK DISORDER ( 6 FDA reports)
BENIGN BONE NEOPLASM ( 6 FDA reports)
BENIGN NEOPLASM OF THYROID GLAND ( 6 FDA reports)
BILE DUCT STONE ( 6 FDA reports)
BILIARY COLIC ( 6 FDA reports)
BIOPSY BREAST ABNORMAL ( 6 FDA reports)
BLOOD PRESSURE INADEQUATELY CONTROLLED ( 6 FDA reports)
BONE FISTULA ( 6 FDA reports)
BONE MARROW DISORDER ( 6 FDA reports)
BORDERLINE PERSONALITY DISORDER ( 6 FDA reports)
BRACHIAL PLEXOPATHY ( 6 FDA reports)
BRAIN OEDEMA ( 6 FDA reports)
BREAST CANCER IN SITU ( 6 FDA reports)
CARDIAC TAMPONADE ( 6 FDA reports)
CARDIO-RESPIRATORY ARREST ( 6 FDA reports)
CARDIOVASCULAR DISORDER ( 6 FDA reports)
CATHETER SITE RELATED REACTION ( 6 FDA reports)
CELLULITIS STREPTOCOCCAL ( 6 FDA reports)
CERVICAL NEURITIS ( 6 FDA reports)
CHEST WALL PAIN ( 6 FDA reports)
CHOLANGIECTASIS ACQUIRED ( 6 FDA reports)
CHRONIC TONSILLITIS ( 6 FDA reports)
COLON NEOPLASM ( 6 FDA reports)
DEFAECATION URGENCY ( 6 FDA reports)
DENTAL CLEANING ( 6 FDA reports)
DIAPHRAGMATIC HERNIA ( 6 FDA reports)
DIAPHRAGMATIC PARALYSIS ( 6 FDA reports)
DISSEMINATED INTRAVASCULAR COAGULATION ( 6 FDA reports)
DISTURBANCE IN SOCIAL BEHAVIOUR ( 6 FDA reports)
DRUG WITHDRAWAL SYNDROME ( 6 FDA reports)
DYSPLASTIC NAEVUS SYNDROME ( 6 FDA reports)
DYSSTASIA ( 6 FDA reports)
ENCEPHALOPATHY ( 6 FDA reports)
ENDOMETRIAL HYPERPLASIA ( 6 FDA reports)
ENTEROCOCCAL INFECTION ( 6 FDA reports)
EOSINOPHILIA ( 6 FDA reports)
EPILEPSY ( 6 FDA reports)
ERYSIPELAS ( 6 FDA reports)
ESCHERICHIA SEPSIS ( 6 FDA reports)
FEMORAL NECK FRACTURE ( 6 FDA reports)
FINGER DEFORMITY ( 6 FDA reports)
FRACTURED SACRUM ( 6 FDA reports)
GANGRENE ( 6 FDA reports)
GASTRITIS EROSIVE ( 6 FDA reports)
GASTROINTESTINAL TUBE INSERTION ( 6 FDA reports)
GENERALISED ANXIETY DISORDER ( 6 FDA reports)
GENITAL HERPES ( 6 FDA reports)
GIANT CELL EPULIS ( 6 FDA reports)
GINGIVAL BLISTER ( 6 FDA reports)
HAEMODIALYSIS ( 6 FDA reports)
ILEAL STENOSIS ( 6 FDA reports)
ILEUS ( 6 FDA reports)
IMPLANT SITE REACTION ( 6 FDA reports)
INSPIRATORY CAPACITY DECREASED ( 6 FDA reports)
INTERMITTENT CLAUDICATION ( 6 FDA reports)
INTESTINAL ULCER ( 6 FDA reports)
INTRACRANIAL ANEURYSM ( 6 FDA reports)
INTRAOCULAR PRESSURE INCREASED ( 6 FDA reports)
LARGE INTESTINAL ULCER ( 6 FDA reports)
LEIOMYOMA ( 6 FDA reports)
LIP AND/OR ORAL CAVITY CANCER ( 6 FDA reports)
LIP NEOPLASM ( 6 FDA reports)
LIP SWELLING ( 6 FDA reports)
LOWER EXTREMITY MASS ( 6 FDA reports)
LUMBAR VERTEBRAL FRACTURE ( 6 FDA reports)
MALIGNANT ASCITES ( 6 FDA reports)
MELAENA ( 6 FDA reports)
MENINGEAL DISORDER ( 6 FDA reports)
MENINGITIS ( 6 FDA reports)
MENISCUS LESION ( 6 FDA reports)
METASTASES TO SOFT TISSUE ( 6 FDA reports)
MICROCYTIC ANAEMIA ( 6 FDA reports)
MODIFIED RADICAL MASTECTOMY ( 6 FDA reports)
MOVEMENT DISORDER ( 6 FDA reports)
MUSCLE DISORDER ( 6 FDA reports)
NEPHROGENIC ANAEMIA ( 6 FDA reports)
NEUROGENIC BLADDER ( 6 FDA reports)
NEUTROPHIL COUNT DECREASED ( 6 FDA reports)
OBSTRUCTION ( 6 FDA reports)
OFF LABEL USE ( 6 FDA reports)
ONYCHOLYSIS ( 6 FDA reports)
ORAL INTAKE REDUCED ( 6 FDA reports)
OVARIAN FAILURE ( 6 FDA reports)
PANCREATIC NEOPLASM ( 6 FDA reports)
PARACENTESIS ( 6 FDA reports)
PARANASAL SINUS MUCOSAL HYPERTROPHY ( 6 FDA reports)
PERITONSILLAR ABSCESS ( 6 FDA reports)
PHARYNGEAL MASS ( 6 FDA reports)
PHARYNGEAL OEDEMA ( 6 FDA reports)
POOR DENTAL CONDITION ( 6 FDA reports)
POOR PERSONAL HYGIENE ( 6 FDA reports)
POST PROCEDURAL HAEMORRHAGE ( 6 FDA reports)
PSEUDOEPITHELIOMATOUS HYPERPLASIA ( 6 FDA reports)
REHABILITATION THERAPY ( 6 FDA reports)
RESPIRATORY TRACT INFECTION ( 6 FDA reports)
RETINAL VEIN OCCLUSION ( 6 FDA reports)
SKIN NECROSIS ( 6 FDA reports)
SKIN NEOPLASM EXCISION ( 6 FDA reports)
TAENIASIS ( 6 FDA reports)
TEETH BRITTLE ( 6 FDA reports)
THROMBOCYTOSIS ( 6 FDA reports)
THYROID DISORDER ( 6 FDA reports)
TOXIC SKIN ERUPTION ( 6 FDA reports)
TRANSFERRIN DECREASED ( 6 FDA reports)
TRAUMATIC HAEMATOMA ( 6 FDA reports)
UMBILICAL HERNIA ( 6 FDA reports)
URINE ANALYSIS ABNORMAL ( 6 FDA reports)
UTERINE ATONY ( 6 FDA reports)
UTERINE POLYP ( 6 FDA reports)
VASOSPASM ( 6 FDA reports)
VENTRICULAR TACHYCARDIA ( 6 FDA reports)
VISUAL PATHWAY DISORDER ( 6 FDA reports)
ANAEMIA POSTOPERATIVE ( 5 FDA reports)
ANAL SPHINCTER ATONY ( 5 FDA reports)
ANASTOMOTIC LEAK ( 5 FDA reports)
ATRIAL SEPTAL DEFECT ( 5 FDA reports)
BILIARY DYSKINESIA ( 5 FDA reports)
BIOPSY SITE UNSPECIFIED ABNORMAL ( 5 FDA reports)
BLADDER DIVERTICULUM ( 5 FDA reports)
BLOOD ALBUMIN DECREASED ( 5 FDA reports)
BLOOD GLUCOSE ABNORMAL ( 5 FDA reports)
BLOOD URIC ACID INCREASED ( 5 FDA reports)
BRADYCARDIA ( 5 FDA reports)
BREAST DISORDER ( 5 FDA reports)
BRONCHOSPASM ( 5 FDA reports)
BURNS FIRST DEGREE ( 5 FDA reports)
CALCULUS URETERIC ( 5 FDA reports)
CEREBROSPINAL FLUID RESERVOIR PLACEMENT ( 5 FDA reports)
CERVICAL POLYP ( 5 FDA reports)
CERVICITIS ( 5 FDA reports)
CHORIORETINOPATHY ( 5 FDA reports)
CLAVICLE FRACTURE ( 5 FDA reports)
COELIAC DISEASE ( 5 FDA reports)
COLITIS ULCERATIVE ( 5 FDA reports)
COLON CANCER ( 5 FDA reports)
COLONIC OBSTRUCTION ( 5 FDA reports)
DEMYELINATION ( 5 FDA reports)
DENTAL DISCOMFORT ( 5 FDA reports)
DERMATITIS ALLERGIC ( 5 FDA reports)
DIABETIC FOOT INFECTION ( 5 FDA reports)
DIPLEGIA ( 5 FDA reports)
DRUG DOSE OMISSION ( 5 FDA reports)
DYSKINESIA OESOPHAGEAL ( 5 FDA reports)
EAR CANAL ERYTHEMA ( 5 FDA reports)
ELECTROCARDIOGRAM T WAVE INVERSION ( 5 FDA reports)
ENDOMETRIAL CANCER ( 5 FDA reports)
EYE INFLAMMATION ( 5 FDA reports)
FAECALOMA ( 5 FDA reports)
FURUNCLE ( 5 FDA reports)
GASTRIC DISORDER ( 5 FDA reports)
GINGIVAL HYPERPLASIA ( 5 FDA reports)
GINGIVAL OPERATION ( 5 FDA reports)
HAEMOLYTIC ANAEMIA ( 5 FDA reports)
HALLUCINATION, VISUAL ( 5 FDA reports)
HEPATITIS FULMINANT ( 5 FDA reports)
HEPATITIS TOXIC ( 5 FDA reports)
HISTOPLASMOSIS ( 5 FDA reports)
HYPERTHERMIA ( 5 FDA reports)
HYPERTRICHOSIS ( 5 FDA reports)
HYPOGAMMAGLOBULINAEMIA ( 5 FDA reports)
IMMUNOSUPPRESSION ( 5 FDA reports)
INCORRECT DOSE ADMINISTERED ( 5 FDA reports)
INGUINAL HERNIA STRANGULATED ( 5 FDA reports)
INTESTINAL FUNCTIONAL DISORDER ( 5 FDA reports)
JOINT CREPITATION ( 5 FDA reports)
LYMPH NODE FIBROSIS ( 5 FDA reports)
MECHANICAL VENTILATION ( 5 FDA reports)
METASTASES TO PERITONEUM ( 5 FDA reports)
METASTASES TO THE MEDIASTINUM ( 5 FDA reports)
MIDDLE INSOMNIA ( 5 FDA reports)
MONOPARESIS ( 5 FDA reports)
MUCOUS MEMBRANE DISORDER ( 5 FDA reports)
MUSCLE TWITCHING ( 5 FDA reports)
NERVE INJURY ( 5 FDA reports)
OCULAR ICTERUS ( 5 FDA reports)
OPTIC NEURITIS ( 5 FDA reports)
ORBITAL OEDEMA ( 5 FDA reports)
OSTEOMYELITIS ACUTE ( 5 FDA reports)
OSTEOSARCOMA METASTATIC ( 5 FDA reports)
PARAPARESIS ( 5 FDA reports)
PAROTITIS ( 5 FDA reports)
PELVIC NEOPLASM ( 5 FDA reports)
PHARMACEUTICAL PRODUCT COMPLAINT ( 5 FDA reports)
PNEUMONITIS CHEMICAL ( 5 FDA reports)
PUBIS FRACTURE ( 5 FDA reports)
PURPURA ( 5 FDA reports)
RADIATION OESOPHAGITIS ( 5 FDA reports)
RESPIRATORY ARREST ( 5 FDA reports)
RETINAL MELANOMA ( 5 FDA reports)
RETINAL PIGMENT EPITHELIOPATHY ( 5 FDA reports)
SEXUALLY TRANSMITTED DISEASE ( 5 FDA reports)
SKIN HYPERPIGMENTATION ( 5 FDA reports)
SPUTUM DISCOLOURED ( 5 FDA reports)
STAPHYLOCOCCAL SKIN INFECTION ( 5 FDA reports)
SUPRAVENTRICULAR EXTRASYSTOLES ( 5 FDA reports)
THERAPEUTIC RESPONSE DECREASED ( 5 FDA reports)
THORACIC CAVITY DRAINAGE ( 5 FDA reports)
THORACIC OUTLET SYNDROME ( 5 FDA reports)
THYROID CYST ( 5 FDA reports)
TOOTH IMPACTED ( 5 FDA reports)
TRACHEAL STENOSIS ( 5 FDA reports)
TREATMENT NONCOMPLIANCE ( 5 FDA reports)
TUMOUR PAIN ( 5 FDA reports)
TYPE V HYPERLIPIDAEMIA ( 5 FDA reports)
UPPER-AIRWAY COUGH SYNDROME ( 5 FDA reports)
URETERIC DILATATION ( 5 FDA reports)
URETHRAL DISORDER ( 5 FDA reports)
VAGINAL DISCHARGE ( 5 FDA reports)
VIRAL UPPER RESPIRATORY TRACT INFECTION ( 5 FDA reports)
VOCAL CORD DISORDER ( 5 FDA reports)
VULVAL ABSCESS ( 5 FDA reports)
VULVOVAGINAL PRURITUS ( 5 FDA reports)
WOUND SECRETION ( 5 FDA reports)
X-RAY ( 5 FDA reports)
ABDOMINAL TENDERNESS ( 4 FDA reports)
ABSCESS MANAGEMENT ( 4 FDA reports)
ABSCESS RUPTURE ( 4 FDA reports)
ACUTE RESPIRATORY DISTRESS SYNDROME ( 4 FDA reports)
ALPHA HAEMOLYTIC STREPTOCOCCAL INFECTION ( 4 FDA reports)
ALVEOLITIS ( 4 FDA reports)
ANTIMITOCHONDRIAL ANTIBODY POSITIVE ( 4 FDA reports)
ATRIOVENTRICULAR BLOCK SECOND DEGREE ( 4 FDA reports)
ATROPHY ( 4 FDA reports)
BACTERIAL DISEASE CARRIER ( 4 FDA reports)
BENIGN NEOPLASM OF ADRENAL GLAND ( 4 FDA reports)
BLOOD TEST ABNORMAL ( 4 FDA reports)
BODY TEMPERATURE DECREASED ( 4 FDA reports)
BRAIN CANCER METASTATIC ( 4 FDA reports)
BREATH SOUNDS ABNORMAL ( 4 FDA reports)
BRONCHIAL DISORDER ( 4 FDA reports)
BUNION OPERATION ( 4 FDA reports)
CAROTID ARTERY OCCLUSION ( 4 FDA reports)
CATARACT CORTICAL ( 4 FDA reports)
CATHETER REMOVAL ( 4 FDA reports)
CEREBRAL CYST ( 4 FDA reports)
CEREBRAL HAEMORRHAGE ( 4 FDA reports)
CHEILITIS ( 4 FDA reports)
CLOSTRIDIAL INFECTION ( 4 FDA reports)
CLUMSINESS ( 4 FDA reports)
COMPLETED SUICIDE ( 4 FDA reports)
CONGESTIVE CARDIOMYOPATHY ( 4 FDA reports)
CORNEAL DEPOSITS ( 4 FDA reports)
CORONARY ARTERY STENOSIS ( 4 FDA reports)
CUTIS LAXA ( 4 FDA reports)
CYSTITIS BACTERIAL ( 4 FDA reports)
DENTAL PULP DISORDER ( 4 FDA reports)
DILATATION VENTRICULAR ( 4 FDA reports)
DRUG DISPENSING ERROR ( 4 FDA reports)
DRUG INEFFECTIVE FOR UNAPPROVED INDICATION ( 4 FDA reports)
DRUG PRESCRIBING ERROR ( 4 FDA reports)
DRUG TOXICITY ( 4 FDA reports)
ENTHESOPATHY ( 4 FDA reports)
EPSTEIN-BARR VIRUS INFECTION ( 4 FDA reports)
ERYTHROMELALGIA ( 4 FDA reports)
EXTREMITY NECROSIS ( 4 FDA reports)
FACIAL PALSY ( 4 FDA reports)
FACIAL PARESIS ( 4 FDA reports)
FEELING DRUNK ( 4 FDA reports)
FOOD POISONING ( 4 FDA reports)
FRACTURE TREATMENT ( 4 FDA reports)
GASTRIC BYPASS ( 4 FDA reports)
GASTROENTERITIS VIRAL ( 4 FDA reports)
GASTROINTESTINAL STROMAL TUMOUR ( 4 FDA reports)
GENE MUTATION IDENTIFICATION TEST POSITIVE ( 4 FDA reports)
GENERAL ANAESTHESIA ( 4 FDA reports)
GENERALISED OEDEMA ( 4 FDA reports)
GLOSSITIS ( 4 FDA reports)
HAEMOLYSIS ( 4 FDA reports)
HAEMORRHAGE SUBCUTANEOUS ( 4 FDA reports)
HAIR TEXTURE ABNORMAL ( 4 FDA reports)
HEPATIC ENCEPHALOPATHY ( 4 FDA reports)
HEPATIC PAIN ( 4 FDA reports)
HERNIA OBSTRUCTIVE ( 4 FDA reports)
HIGH DENSITY LIPOPROTEIN INCREASED ( 4 FDA reports)
IMPAIRED GASTRIC EMPTYING ( 4 FDA reports)
INADEQUATE ANALGESIA ( 4 FDA reports)
INAPPROPRIATE SCHEDULE OF DRUG ADMINISTRATION ( 4 FDA reports)
INCREASED APPETITE ( 4 FDA reports)
INFUSION SITE SWELLING ( 4 FDA reports)
INSULINOMA ( 4 FDA reports)
INTESTINAL ISCHAEMIA ( 4 FDA reports)
IRIS ADHESIONS ( 4 FDA reports)
JAW CYST ( 4 FDA reports)
LEUKOENCEPHALOPATHY ( 4 FDA reports)
LIVER INJURY ( 4 FDA reports)
LOWER LIMB FRACTURE ( 4 FDA reports)
MACULAR HOLE ( 4 FDA reports)
MACULOPATHY ( 4 FDA reports)
MASTOID DISORDER ( 4 FDA reports)
METASTASES TO CHEST WALL ( 4 FDA reports)
METASTASES TO NECK ( 4 FDA reports)
METASTASES TO SPLEEN ( 4 FDA reports)
MIXED HYPERLIPIDAEMIA ( 4 FDA reports)
NAIL DISCOLOURATION ( 4 FDA reports)
NEPHRITIS ( 4 FDA reports)
NEPHROPATHY ( 4 FDA reports)
NEUROFIBROMA ( 4 FDA reports)
NIGHTMARE ( 4 FDA reports)
NODAL RHYTHM ( 4 FDA reports)
NUCLEAR MAGNETIC RESONANCE IMAGING BRAIN ABNORMAL ( 4 FDA reports)
OBSESSIVE-COMPULSIVE DISORDER ( 4 FDA reports)
OCULAR HYPERTENSION ( 4 FDA reports)
OESOPHAGEAL PAIN ( 4 FDA reports)
ONYCHOCLASIS ( 4 FDA reports)
ONYCHOMADESIS ( 4 FDA reports)
PAPILLOEDEMA ( 4 FDA reports)
PARACENTESIS ABDOMEN ( 4 FDA reports)
PARANEOPLASTIC SYNDROME ( 4 FDA reports)
PERFORMANCE STATUS DECREASED ( 4 FDA reports)
PERSONALITY CHANGE ( 4 FDA reports)
PHARYNGOLARYNGEAL PAIN ( 4 FDA reports)
PIGMENTATION DISORDER ( 4 FDA reports)
PNEUMOCYSTIS JIROVECI PNEUMONIA ( 4 FDA reports)
PO2 DECREASED ( 4 FDA reports)
POLYCYSTIC OVARIES ( 4 FDA reports)
POLYURIA ( 4 FDA reports)
POSTOPERATIVE WOUND INFECTION ( 4 FDA reports)
PSYCHOSOMATIC DISEASE ( 4 FDA reports)
PULMONARY VALVE INCOMPETENCE ( 4 FDA reports)
RADIATION SKIN INJURY ( 4 FDA reports)
RASH GENERALISED ( 4 FDA reports)
RENAL MASS ( 4 FDA reports)
SHOULDER OPERATION ( 4 FDA reports)
SKIN BURNING SENSATION ( 4 FDA reports)
SPHINGOMONAS PAUCIMOBILIS INFECTION ( 4 FDA reports)
SPINAL OPERATION ( 4 FDA reports)
SUBCUTANEOUS EMPHYSEMA ( 4 FDA reports)
SUTURE REMOVAL ( 4 FDA reports)
TENDON RUPTURE ( 4 FDA reports)
TENOSYNOVITIS ( 4 FDA reports)
THERAPEUTIC PROCEDURE ( 4 FDA reports)
THINKING ABNORMAL ( 4 FDA reports)
TOOTH DISCOLOURATION ( 4 FDA reports)
TRANSPLANT ( 4 FDA reports)
URETHRAL HAEMORRHAGE ( 4 FDA reports)
URINARY BLADDER HAEMORRHAGE ( 4 FDA reports)
UTERINE DISORDER ( 4 FDA reports)
VENOUS ANGIOMA OF BRAIN ( 4 FDA reports)
VITH NERVE PARALYSIS ( 4 FDA reports)
WEIGHT ABNORMAL ( 4 FDA reports)
WEIGHT FLUCTUATION ( 4 FDA reports)
WEIGHT LOSS POOR ( 4 FDA reports)
WOUND COMPLICATION ( 4 FDA reports)
ABDOMINAL SYMPTOM ( 3 FDA reports)
ACUTE GENERALISED EXANTHEMATOUS PUSTULOSIS ( 3 FDA reports)
ACUTE PULMONARY OEDEMA ( 3 FDA reports)
ADENOMATOUS POLYPOSIS COLI ( 3 FDA reports)
AGE-RELATED MACULAR DEGENERATION ( 3 FDA reports)
ALBUMIN GLOBULIN RATIO DECREASED ( 3 FDA reports)
ALVEOLITIS ALLERGIC ( 3 FDA reports)
ANORECTAL DISORDER ( 3 FDA reports)
ANTIBIOTIC RESISTANT STAPHYLOCOCCUS TEST POSITIVE ( 3 FDA reports)
APATHY ( 3 FDA reports)
ARTERIAL CATHETERISATION ( 3 FDA reports)
AUTOIMMUNE DISORDER ( 3 FDA reports)
AVULSION FRACTURE ( 3 FDA reports)
BARRETT'S OESOPHAGUS ( 3 FDA reports)
BLEPHARITIS ( 3 FDA reports)
BLOOD AMYLASE INCREASED ( 3 FDA reports)
BLOOD CREATINE PHOSPHOKINASE MM INCREASED ( 3 FDA reports)
BLOOD GLUCOSE DECREASED ( 3 FDA reports)
BLOOD OESTROGEN DECREASED ( 3 FDA reports)
BLOOD UREA DECREASED ( 3 FDA reports)
BONE DENSITY INCREASED ( 3 FDA reports)
BRACHIOCEPHALIC VEIN STENOSIS ( 3 FDA reports)
BREAST HAEMORRHAGE ( 3 FDA reports)
CANCER PAIN ( 3 FDA reports)
CAROTID ARTERY INSUFFICIENCY ( 3 FDA reports)
CATHETER THROMBOSIS ( 3 FDA reports)
CATHETERISATION CARDIAC ( 3 FDA reports)
CEREBRAL THROMBOSIS ( 3 FDA reports)
CHANGE OF BOWEL HABIT ( 3 FDA reports)
CHEST WALL MASS ( 3 FDA reports)
CHOLESTATIC LIVER INJURY ( 3 FDA reports)
CHONDROPATHY ( 3 FDA reports)
CHRONIC LYMPHOCYTIC LEUKAEMIA ( 3 FDA reports)
CLAUSTROPHOBIA ( 3 FDA reports)
COLLAGEN-VASCULAR DISEASE ( 3 FDA reports)
COLPORRHAPHY ( 3 FDA reports)
COORDINATION ABNORMAL ( 3 FDA reports)
CUTANEOUS LUPUS ERYTHEMATOSUS ( 3 FDA reports)
CYCLOTHYMIC DISORDER ( 3 FDA reports)
CYSTITIS NONINFECTIVE ( 3 FDA reports)
DACRYOSTENOSIS ACQUIRED ( 3 FDA reports)
DELUSION ( 3 FDA reports)
DENTAL PLAQUE ( 3 FDA reports)
DERMATOMYOSITIS ( 3 FDA reports)
DEVICE DISLOCATION ( 3 FDA reports)
DIABETIC ENTEROPATHY ( 3 FDA reports)
DIABETIC ULCER ( 3 FDA reports)
DRUG ADMINISTRATION ERROR ( 3 FDA reports)
DYSHIDROSIS ( 3 FDA reports)
DYSTROPHIC CALCIFICATION ( 3 FDA reports)
EAR PRURITUS ( 3 FDA reports)
ELECTROENCEPHALOGRAM ABNORMAL ( 3 FDA reports)
ENTEROCOLITIS ( 3 FDA reports)
EOSINOPHIL COUNT INCREASED ( 3 FDA reports)
EPIGLOTTIC OEDEMA ( 3 FDA reports)
EXTRASYSTOLES ( 3 FDA reports)
FAECES PALE ( 3 FDA reports)
FIBROUS HISTIOCYTOMA ( 3 FDA reports)
FOCAL NODULAR HYPERPLASIA ( 3 FDA reports)
FREQUENT BOWEL MOVEMENTS ( 3 FDA reports)
FUNGAL PARONYCHIA ( 3 FDA reports)
GASTRIC CANCER ( 3 FDA reports)
GASTROINTESTINAL SURGERY ( 3 FDA reports)
GENERAL PHYSICAL CONDITION ABNORMAL ( 3 FDA reports)
GENERALISED ERYTHEMA ( 3 FDA reports)
GENITAL HAEMORRHAGE ( 3 FDA reports)
HAEMATOCRIT INCREASED ( 3 FDA reports)
HAEMATOTOXICITY ( 3 FDA reports)
HAEMORRHAGIC DIATHESIS ( 3 FDA reports)
HEARING IMPAIRED ( 3 FDA reports)
HEPATIC NECROSIS ( 3 FDA reports)
HEPATITIS A ANTIBODY POSITIVE ( 3 FDA reports)
HYPERAMMONAEMIA ( 3 FDA reports)
HYPERTENSIVE CRISIS ( 3 FDA reports)
HYPOTRICHOSIS ( 3 FDA reports)
INJECTION SITE ERYTHEMA ( 3 FDA reports)
INJECTION SITE NODULE ( 3 FDA reports)
INNER EAR DISORDER ( 3 FDA reports)
INTESTINAL POLYP ( 3 FDA reports)
INTRADUCTAL PAPILLOMA OF BREAST ( 3 FDA reports)
IRON DEFICIENCY ( 3 FDA reports)
JUGULAR VEIN THROMBOSIS ( 3 FDA reports)
KNEE DEFORMITY ( 3 FDA reports)
KNEE OPERATION ( 3 FDA reports)
LACK OF SPONTANEOUS SPEECH ( 3 FDA reports)
LARGE INTESTINE FIBROMA ( 3 FDA reports)
LICHEN SCLEROSUS ( 3 FDA reports)
LIGAMENT DISORDER ( 3 FDA reports)
LIPASE INCREASED ( 3 FDA reports)
LUNG WEDGE RESECTION ( 3 FDA reports)
LYMPH NODE PALPABLE ( 3 FDA reports)
LYMPHANGITIS ( 3 FDA reports)
LYMPHOCYTE PERCENTAGE INCREASED ( 3 FDA reports)
MAMMARY DUCT ECTASIA ( 3 FDA reports)
MEDICATION ERROR ( 3 FDA reports)
MENINGITIS ASEPTIC ( 3 FDA reports)
MENOPAUSAL SYMPTOMS ( 3 FDA reports)
METAMORPHOPSIA ( 3 FDA reports)
MONOCYTE PERCENTAGE INCREASED ( 3 FDA reports)
MUSCLE CONTRACTIONS INVOLUNTARY ( 3 FDA reports)
MYELOID LEUKAEMIA ( 3 FDA reports)
MYELOMALACIA ( 3 FDA reports)
NAIL AVULSION ( 3 FDA reports)
NAIL DYSTROPHY ( 3 FDA reports)
NECK MASS ( 3 FDA reports)
NEPHROTIC SYNDROME ( 3 FDA reports)
NEUROLEPTIC MALIGNANT SYNDROME ( 3 FDA reports)
NIPPLE EXUDATE BLOODY ( 3 FDA reports)
NIPPLE PAIN ( 3 FDA reports)
NO THERAPEUTIC RESPONSE ( 3 FDA reports)
NON-SMALL CELL LUNG CANCER METASTATIC ( 3 FDA reports)
NON-SMALL CELL LUNG CANCER RECURRENT ( 3 FDA reports)
OCULAR NEOPLASM ( 3 FDA reports)
OPTIC ISCHAEMIC NEUROPATHY ( 3 FDA reports)
ORAL MUCOSA EROSION ( 3 FDA reports)
ORAL MUCOSAL ERYTHEMA ( 3 FDA reports)
OVARIAN ENLARGEMENT ( 3 FDA reports)
PALLIATIVE CARE ( 3 FDA reports)
PARANASAL CYST ( 3 FDA reports)
PARONYCHIA ( 3 FDA reports)
PECTUS EXCAVATUM ( 3 FDA reports)
PERIORBITAL HAEMATOMA ( 3 FDA reports)
PERIPHERAL COLDNESS ( 3 FDA reports)
PORTAL VEIN THROMBOSIS ( 3 FDA reports)
POSTMENOPAUSE ( 3 FDA reports)
PRECANCEROUS CELLS PRESENT ( 3 FDA reports)
PRESBYACUSIS ( 3 FDA reports)
PRESBYOPIA ( 3 FDA reports)
PROTEUS INFECTION ( 3 FDA reports)
PROTHROMBIN TIME SHORTENED ( 3 FDA reports)
PULMONARY ARTERY THROMBOSIS ( 3 FDA reports)
PYELOCALIECTASIS ( 3 FDA reports)
RADIATION FIBROSIS ( 3 FDA reports)
RED BLOOD CELL SEDIMENTATION RATE INCREASED ( 3 FDA reports)
RENAL ANEURYSM ( 3 FDA reports)
RETINAL DISORDER ( 3 FDA reports)
RETINAL ISCHAEMIA ( 3 FDA reports)
RETROPERITONEAL HAEMATOMA ( 3 FDA reports)
SCAPULA FRACTURE ( 3 FDA reports)
SECONDARY SEQUESTRUM ( 3 FDA reports)
SENSORY DISTURBANCE ( 3 FDA reports)
SINUS POLYP ( 3 FDA reports)
SKIN INJURY ( 3 FDA reports)
SKIN IRRITATION ( 3 FDA reports)
SKIN NODULE ( 3 FDA reports)
SPLENIC ARTERY ANEURYSM ( 3 FDA reports)
SPLENIC CYST ( 3 FDA reports)
SQUAMOUS CELL CARCINOMA OF SKIN ( 3 FDA reports)
STERNAL FRACTURE ( 3 FDA reports)
THROAT IRRITATION ( 3 FDA reports)
THROMBOPHLEBITIS SUPERFICIAL ( 3 FDA reports)
TOOTH HYPOPLASIA ( 3 FDA reports)
TUBULOINTERSTITIAL NEPHRITIS ( 3 FDA reports)
UVEITIS ( 3 FDA reports)
VAGINITIS BACTERIAL ( 3 FDA reports)
VAGINOPLASTY ( 3 FDA reports)
VASCULAR OCCLUSION ( 3 FDA reports)
VASCULITIC RASH ( 3 FDA reports)
VEIN DISORDER ( 3 FDA reports)
VENA CAVA THROMBOSIS ( 3 FDA reports)
VULVAL LEUKOPLAKIA ( 3 FDA reports)
VULVOVAGINAL DISCOMFORT ( 3 FDA reports)
VULVOVAGINAL MYCOTIC INFECTION ( 3 FDA reports)
WRONG TECHNIQUE IN DRUG USAGE PROCESS ( 3 FDA reports)
ABNORMAL DREAMS ( 2 FDA reports)
ABNORMAL FAECES ( 2 FDA reports)
ACANTHOSIS ( 2 FDA reports)
ACUTE MYOCARDIAL INFARCTION ( 2 FDA reports)
ACUTE RESPIRATORY FAILURE ( 2 FDA reports)
ADJUSTMENT DISORDER ( 2 FDA reports)
ADVERSE DRUG REACTION ( 2 FDA reports)
ANAEMIA HAEMOLYTIC AUTOIMMUNE ( 2 FDA reports)
ANAL POLYP ( 2 FDA reports)
ANGIONEUROTIC OEDEMA ( 2 FDA reports)
ANTIDIURETIC HORMONE ABNORMALITY ( 2 FDA reports)
ANTINUCLEAR ANTIBODY INCREASED ( 2 FDA reports)
APLASIA ( 2 FDA reports)
APNOEIC ATTACK ( 2 FDA reports)
APPARENT DEATH ( 2 FDA reports)
ASPERGILLOSIS ( 2 FDA reports)
ASTERIXIS ( 2 FDA reports)
ATRIOVENTRICULAR BLOCK FIRST DEGREE ( 2 FDA reports)
AZYGOS LOBE ( 2 FDA reports)
B-CELL LYMPHOMA ( 2 FDA reports)
BASILAR ARTERY STENOSIS ( 2 FDA reports)
BENIGN BREAST NEOPLASM ( 2 FDA reports)
BILE DUCT STENT INSERTION ( 2 FDA reports)
BILIARY TRACT DISORDER ( 2 FDA reports)
BILIRUBIN CONJUGATED ( 2 FDA reports)
BIOPSY STOMACH ( 2 FDA reports)
BLADDER CANCER ( 2 FDA reports)
BLOOD CALCIUM ABNORMAL ( 2 FDA reports)
BLOOD CORTISOL INCREASED ( 2 FDA reports)
BLOOD PRESSURE ( 2 FDA reports)
BLOOD PRESSURE ABNORMAL ( 2 FDA reports)
BLOOD PRESSURE DIASTOLIC INCREASED ( 2 FDA reports)
BLOOD PRESSURE SYSTOLIC DECREASED ( 2 FDA reports)
BONE NEOPLASM ( 2 FDA reports)
BOWEL MOVEMENT IRREGULARITY ( 2 FDA reports)
BREAST CANCER STAGE II ( 2 FDA reports)
BREAST CELLULITIS ( 2 FDA reports)
BREAST INDURATION ( 2 FDA reports)
BURNS THIRD DEGREE ( 2 FDA reports)
BUTTOCK PAIN ( 2 FDA reports)
CALCIFIC DEPOSITS REMOVAL ( 2 FDA reports)
CARBOHYDRATE ANTIGEN 125 INCREASED ( 2 FDA reports)
CARDIAC OPERATION ( 2 FDA reports)
CARDIAC VALVE DISEASE ( 2 FDA reports)
CARDIOGENIC SHOCK ( 2 FDA reports)
CARDIOPULMONARY FAILURE ( 2 FDA reports)
CATHETER SITE PAIN ( 2 FDA reports)
CELL MARKER INCREASED ( 2 FDA reports)
CEREBELLAR ATAXIA ( 2 FDA reports)
CHOKING ( 2 FDA reports)
CHOLANGITIS ( 2 FDA reports)
CHONDROMALACIA ( 2 FDA reports)
CHORIORETINAL ATROPHY ( 2 FDA reports)
CHRONIC HEPATITIS ( 2 FDA reports)
CHRONIC OBSTRUCTIVE AIRWAYS DISEASE ( 2 FDA reports)
CLONUS ( 2 FDA reports)
COAGULOPATHY ( 2 FDA reports)
COLITIS EROSIVE ( 2 FDA reports)
COLLAGEN DISORDER ( 2 FDA reports)
COLONOSCOPY ( 2 FDA reports)
COMA HEPATIC ( 2 FDA reports)
CONJUNCTIVAL HAEMORRHAGE ( 2 FDA reports)
CONVERSION DISORDER ( 2 FDA reports)
CORONARY ARTERY OCCLUSION ( 2 FDA reports)
CRANIOCEREBRAL INJURY ( 2 FDA reports)
CREATININE RENAL CLEARANCE DECREASED ( 2 FDA reports)
DECREASED ACTIVITY ( 2 FDA reports)
DERMATITIS ACNEIFORM ( 2 FDA reports)
DERMATITIS EXFOLIATIVE ( 2 FDA reports)
DIABETIC RETINOPATHY ( 2 FDA reports)
DILATATION ATRIAL ( 2 FDA reports)
DROP ATTACKS ( 2 FDA reports)
DRUG ADMINISTERED AT INAPPROPRIATE SITE ( 2 FDA reports)
DRUG EFFECT DECREASED ( 2 FDA reports)
DYSKINESIA ( 2 FDA reports)
EATING DISORDER SYMPTOM ( 2 FDA reports)
ECHOCARDIOGRAM ABNORMAL ( 2 FDA reports)
ENANTHEMA ( 2 FDA reports)
ENTEROCOLITIS HAEMORRHAGIC ( 2 FDA reports)
ENTEROVESICAL FISTULA ( 2 FDA reports)
EPIDERMOLYSIS ( 2 FDA reports)
ERYTHROPENIA ( 2 FDA reports)
EXERCISE TOLERANCE DECREASED ( 2 FDA reports)
EYE HAEMORRHAGE ( 2 FDA reports)
EYE OEDEMA ( 2 FDA reports)
FIBROADENOMA OF BREAST ( 2 FDA reports)
FINE MOTOR DELAY ( 2 FDA reports)
FLANK PAIN ( 2 FDA reports)
FRUCTOSAMINE INCREASED ( 2 FDA reports)
FUNCTIONAL GASTROINTESTINAL DISORDER ( 2 FDA reports)
GASTRIC HAEMORRHAGE ( 2 FDA reports)
GINGIVECTOMY ( 2 FDA reports)
GRANULOCYTOPENIA ( 2 FDA reports)
HAEMOGLOBIN INCREASED ( 2 FDA reports)
HAEMORRHAGIC CEREBRAL INFARCTION ( 2 FDA reports)
HAEMORRHOIDAL HAEMORRHAGE ( 2 FDA reports)
HAIR DISORDER ( 2 FDA reports)
HEAD DISCOMFORT ( 2 FDA reports)
HEAD TITUBATION ( 2 FDA reports)
HEART INJURY ( 2 FDA reports)
HEMIPLEGIA ( 2 FDA reports)
HEPATIC ENZYME ABNORMAL ( 2 FDA reports)
HEPATITIS ACUTE ( 2 FDA reports)
HEPATOCELLULAR INJURY ( 2 FDA reports)
HYPERAEMIA ( 2 FDA reports)
HYPERCAPNIA ( 2 FDA reports)
HYPERMETROPIA ( 2 FDA reports)
HYPOCHROMIC ANAEMIA ( 2 FDA reports)
HYPOPROTEINAEMIA ( 2 FDA reports)
HYPOTONIA ( 2 FDA reports)
IMPAIRED SELF-CARE ( 2 FDA reports)
IMPAIRED WORK ABILITY ( 2 FDA reports)
INCISION SITE COMPLICATION ( 2 FDA reports)
INCISION SITE ERYTHEMA ( 2 FDA reports)
INCISION SITE OEDEMA ( 2 FDA reports)
INCORRECT DRUG ADMINISTRATION DURATION ( 2 FDA reports)
INCREASED UPPER AIRWAY SECRETION ( 2 FDA reports)
INFECTIOUS PERITONITIS ( 2 FDA reports)
INFUSION SITE REACTION ( 2 FDA reports)
INJECTION SITE HAEMORRHAGE ( 2 FDA reports)
INJECTION SITE PAIN ( 2 FDA reports)
INTERNATIONAL NORMALISED RATIO ( 2 FDA reports)
INTERTRIGO ( 2 FDA reports)
INTESTINAL OBSTRUCTION ( 2 FDA reports)
INTESTINAL PERFORATION ( 2 FDA reports)
INTRACRANIAL HYPOTENSION ( 2 FDA reports)
INTRAMEDULLARY ROD INSERTION ( 2 FDA reports)
INTRAOCULAR PRESSURE FLUCTUATION ( 2 FDA reports)
ISCHAEMIC CARDIOMYOPATHY ( 2 FDA reports)
JAW LESION EXCISION ( 2 FDA reports)
KERATITIS ( 2 FDA reports)
LABORATORY TEST ABNORMAL ( 2 FDA reports)
LEFT VENTRICULAR FAILURE ( 2 FDA reports)
LEUKOARAIOSIS ( 2 FDA reports)
LIBIDO INCREASED ( 2 FDA reports)
LIMB INJURY ( 2 FDA reports)
LIP DISORDER ( 2 FDA reports)
LOSS OF EMPLOYMENT ( 2 FDA reports)
LYMPH NODE CANCER METASTATIC ( 2 FDA reports)
LYMPHOPENIA ( 2 FDA reports)
MACROSOMIA ( 2 FDA reports)
MACULAR CYST ( 2 FDA reports)
MALIGNANT MESENTERIC NEOPLASM ( 2 FDA reports)
MARITAL PROBLEM ( 2 FDA reports)
MENINGISM ( 2 FDA reports)
MENTAL IMPAIRMENT ( 2 FDA reports)
METASTASES TO RETROPERITONEUM ( 2 FDA reports)
MONOPLEGIA ( 2 FDA reports)
MUCOUS STOOLS ( 2 FDA reports)
MYELOPROLIFERATIVE DISORDER ( 2 FDA reports)
MYOCARDIAL ISCHAEMIA ( 2 FDA reports)
MYOCLONUS ( 2 FDA reports)
NECROTISING SCLERITIS ( 2 FDA reports)
NEPHROGENIC DIABETES INSIPIDUS ( 2 FDA reports)
NEURITIS ( 2 FDA reports)
NOCTURNAL DYSPNOEA ( 2 FDA reports)
NORMOCHROMIC NORMOCYTIC ANAEMIA ( 2 FDA reports)
OCCIPITAL NEURALGIA ( 2 FDA reports)
OEDEMA DUE TO CARDIAC DISEASE ( 2 FDA reports)
OESTROGEN DEFICIENCY ( 2 FDA reports)
OLIGURIA ( 2 FDA reports)
OMENTECTOMY ( 2 FDA reports)
OMENTUM NEOPLASM ( 2 FDA reports)
ONYCHALGIA ( 2 FDA reports)
OPEN ANGLE GLAUCOMA ( 2 FDA reports)
ORAL BACTERIAL INFECTION ( 2 FDA reports)
ORAL DYSAESTHESIA ( 2 FDA reports)
ORAL PUSTULE ( 2 FDA reports)
ORGAN FAILURE ( 2 FDA reports)
OSTEOPOROTIC FRACTURE ( 2 FDA reports)
OTOTOXICITY ( 2 FDA reports)
OVARIAN ADENOMA ( 2 FDA reports)
OVARIAN HAEMATOMA ( 2 FDA reports)
PANCREATIC INSUFFICIENCY ( 2 FDA reports)
PARAPSORIASIS ( 2 FDA reports)
PARTIAL SEIZURES ( 2 FDA reports)
PARTNER STRESS ( 2 FDA reports)
PATHOGEN RESISTANCE ( 2 FDA reports)
PERIANAL ERYTHEMA ( 2 FDA reports)
PERITONEAL CYST ( 2 FDA reports)
PHOTOPSIA ( 2 FDA reports)
PNEUMONECTOMY ( 2 FDA reports)
POST INFLAMMATORY PIGMENTATION CHANGE ( 2 FDA reports)
PRESENILE DEMENTIA ( 2 FDA reports)
PRODUCT SUBSTITUTION ISSUE ( 2 FDA reports)
PROTEIN TOTAL ABNORMAL ( 2 FDA reports)
PROTHROMBIN TIME ABNORMAL ( 2 FDA reports)
PSYCHOMOTOR HYPERACTIVITY ( 2 FDA reports)
PSYCHOTIC DISORDER DUE TO A GENERAL MEDICAL CONDITION ( 2 FDA reports)
PULMONARY ALVEOLAR HAEMORRHAGE ( 2 FDA reports)
PULMONARY ARTERIAL HYPERTENSION ( 2 FDA reports)
PULMONARY INFARCTION ( 2 FDA reports)
RADIATION NECROSIS ( 2 FDA reports)
RASH PAPULAR ( 2 FDA reports)
RASH PUSTULAR ( 2 FDA reports)
RED BLOOD CELL COUNT INCREASED ( 2 FDA reports)
REFLUX GASTRITIS ( 2 FDA reports)
REFUSAL OF TREATMENT BY PATIENT ( 2 FDA reports)
RENAL CELL CARCINOMA STAGE UNSPECIFIED ( 2 FDA reports)
RETROPERITONEAL FIBROSIS ( 2 FDA reports)
RIGHT VENTRICULAR DYSFUNCTION ( 2 FDA reports)
SCAB ( 2 FDA reports)
SCAN LYMPH NODES ( 2 FDA reports)
SCLERODERMA ( 2 FDA reports)
SHOCK ( 2 FDA reports)
SINUS ARREST ( 2 FDA reports)
SINUSITIS FUNGAL ( 2 FDA reports)
SKIN FISSURES ( 2 FDA reports)
SKIN FLAP NECROSIS ( 2 FDA reports)
SKIN HAEMORRHAGE ( 2 FDA reports)
SKIN WARM ( 2 FDA reports)
SLEEP TALKING ( 2 FDA reports)
SMALL INTESTINAL PERFORATION ( 2 FDA reports)
SPINAL CORD DISORDER ( 2 FDA reports)
SPINAL MENINGEAL CYST ( 2 FDA reports)
SPLEEN SCAN ABNORMAL ( 2 FDA reports)
STREPTOCOCCAL SEPSIS ( 2 FDA reports)
STRESS FRACTURE ( 2 FDA reports)
SUBARACHNOID HAEMORRHAGE ( 2 FDA reports)
SUDDEN DEATH ( 2 FDA reports)
SUDDEN HEARING LOSS ( 2 FDA reports)
SUPERINFECTION ( 2 FDA reports)
SYMBOLIC DYSFUNCTION ( 2 FDA reports)
SYNOVIAL DISORDER ( 2 FDA reports)
SYRINGOMYELIA ( 2 FDA reports)
TEMPERATURE INTOLERANCE ( 2 FDA reports)
TERMINAL STATE ( 2 FDA reports)
THORACOTOMY ( 2 FDA reports)
THROMBOSIS IN DEVICE ( 2 FDA reports)
TIBIA FRACTURE ( 2 FDA reports)
TONGUE DISCOLOURATION ( 2 FDA reports)
TOXIC ENCEPHALOPATHY ( 2 FDA reports)
TOXICITY TO VARIOUS AGENTS ( 2 FDA reports)
TYPE 1 DIABETES MELLITUS ( 2 FDA reports)
VASCULAR PURPURA ( 2 FDA reports)
VEIN PAIN ( 2 FDA reports)
VENOUS ANEURYSM ( 2 FDA reports)
VERTIGO POSITIONAL ( 2 FDA reports)
VESTIBULITIS ( 2 FDA reports)
VISUAL FIELD DEFECT ( 2 FDA reports)
VITAMIN D DEFICIENCY ( 2 FDA reports)
VITREOUS HAEMORRHAGE ( 2 FDA reports)
VOCAL CORD POLYP ( 2 FDA reports)
VULVAL HAEMORRHAGE ( 2 FDA reports)
VULVOVAGINAL BURNING SENSATION ( 2 FDA reports)
WHOLE BLOOD TRANSFUSION ( 2 FDA reports)
WITHDRAWAL SYNDROME ( 2 FDA reports)
XEROSIS ( 2 FDA reports)
ABDOMINAL MASS ( 1 FDA reports)
ABDOMINAL NEOPLASM ( 1 FDA reports)
ABDOMINAL OPERATION ( 1 FDA reports)
ABDOMINAL WALL CYST ( 1 FDA reports)
ABSCESS LIMB ( 1 FDA reports)
ACCIDENT ( 1 FDA reports)
ACCIDENT AT HOME ( 1 FDA reports)
ACCOMMODATION DISORDER ( 1 FDA reports)
ACIDOSIS ( 1 FDA reports)
ACNE CYSTIC ( 1 FDA reports)
ACUTE ABDOMEN ( 1 FDA reports)
ACUTE CORONARY SYNDROME ( 1 FDA reports)
ACUTE LEUKAEMIA ( 1 FDA reports)
ACUTE MONOCYTIC LEUKAEMIA ( 1 FDA reports)
ADENOCARCINOMA PANCREAS ( 1 FDA reports)
ADENOMYOSIS ( 1 FDA reports)
ADRENAL CORTICAL INSUFFICIENCY ( 1 FDA reports)
ADRENOCORTICAL INSUFFICIENCY CHRONIC ( 1 FDA reports)
ADVERSE EVENT ( 1 FDA reports)
ADVERSE REACTION ( 1 FDA reports)
ALANINE AMINOTRANSFERASE ( 1 FDA reports)
ALBUMIN GLOBULIN RATIO INCREASED ( 1 FDA reports)
ALCOHOL USE ( 1 FDA reports)
AMMONIA INCREASED ( 1 FDA reports)
AMYOTROPHIC LATERAL SCLEROSIS ( 1 FDA reports)
ANAL FISSURE ( 1 FDA reports)
ANAPHYLACTIC REACTION ( 1 FDA reports)
ANGIOGRAM ABNORMAL ( 1 FDA reports)
ANORECTAL DISCOMFORT ( 1 FDA reports)
ANTIPHOSPHOLIPID ANTIBODIES ( 1 FDA reports)
ANXIETY DISORDER ( 1 FDA reports)
APNOEA ( 1 FDA reports)
ARTERIAL DISORDER ( 1 FDA reports)
ARTERIAL OCCLUSIVE DISEASE ( 1 FDA reports)
ARTERIAL THROMBOSIS ( 1 FDA reports)
ARTERIAL THROMBOSIS LIMB ( 1 FDA reports)
ARTERIOVENOUS MALFORMATION ( 1 FDA reports)
ASPARTATE AMINOTRANSFERASE ( 1 FDA reports)
ASPIRATION BONE MARROW ABNORMAL ( 1 FDA reports)
ASPIRATION JOINT ( 1 FDA reports)
ASTHENOPIA ( 1 FDA reports)
ATAXIA ( 1 FDA reports)
ATYPICAL FEMUR FRACTURE ( 1 FDA reports)
AURA ( 1 FDA reports)
AUTOANTIBODY POSITIVE ( 1 FDA reports)
AXILLARY PAIN ( 1 FDA reports)
AXONAL NEUROPATHY ( 1 FDA reports)
BENIGN HEPATIC NEOPLASM ( 1 FDA reports)
BENIGN HYDATIDIFORM MOLE ( 1 FDA reports)
BIOPSY MUCOSA ABNORMAL ( 1 FDA reports)
BIOPSY PALATE ABNORMAL ( 1 FDA reports)
BITE ( 1 FDA reports)
BLOOD ANDROSTENEDIONE INCREASED ( 1 FDA reports)
BLOOD CHLORIDE DECREASED ( 1 FDA reports)
BLOOD CHOLESTEROL ABNORMAL ( 1 FDA reports)
BLOOD CREATINE PHOSPHOKINASE MB ( 1 FDA reports)
BLOOD CREATININE ABNORMAL ( 1 FDA reports)
BLOOD CULTURE POSITIVE ( 1 FDA reports)
BLOOD DISORDER ( 1 FDA reports)
BLOOD MAGNESIUM INCREASED ( 1 FDA reports)
BLOOD OESTROGEN INCREASED ( 1 FDA reports)
BLOOD PHOSPHORUS DECREASED ( 1 FDA reports)
BLOOD PHOSPHORUS INCREASED ( 1 FDA reports)
BLOOD POTASSIUM INCREASED ( 1 FDA reports)
BLOOD PROLACTIN INCREASED ( 1 FDA reports)
BLOOD THYROID STIMULATING HORMONE INCREASED ( 1 FDA reports)
BLOOD TRIGLYCERIDES ABNORMAL ( 1 FDA reports)
BLOODY DISCHARGE ( 1 FDA reports)
BONE CANCER METASTATIC ( 1 FDA reports)
BONE DENSITY ABNORMAL ( 1 FDA reports)
BONE FORMATION DECREASED ( 1 FDA reports)
BONE FRAGMENTATION AROUND IMPLANT ( 1 FDA reports)
BONE INFECTION ( 1 FDA reports)
BONE MARROW DEPRESSION ( 1 FDA reports)
BONE MARROW TOXICITY ( 1 FDA reports)
BONE MARROW TUMOUR CELL INFILTRATION ( 1 FDA reports)
BRADYARRHYTHMIA ( 1 FDA reports)
BRAIN COMPRESSION ( 1 FDA reports)
BRAIN STEM HAEMORRHAGE ( 1 FDA reports)
BRAIN STEM SYNDROME ( 1 FDA reports)
BREAST CANCER STAGE III ( 1 FDA reports)
BREAST DISCOMFORT ( 1 FDA reports)
BREAST INFECTION ( 1 FDA reports)
BREAST NEOPLASM ( 1 FDA reports)
BRONCHIAL IRRITATION ( 1 FDA reports)
BUNDLE BRANCH BLOCK ( 1 FDA reports)
CARBOHYDRATE ANTIGEN 15-3 INCREASED ( 1 FDA reports)
CARDIAC DEATH ( 1 FDA reports)
CARDIAC FAILURE CHRONIC ( 1 FDA reports)
CARDIAC FUNCTION TEST ABNORMAL ( 1 FDA reports)
CARDIOACTIVE DRUG LEVEL INCREASED ( 1 FDA reports)
CARDIOTOXICITY ( 1 FDA reports)
CAROTID ARTERY ATHEROMA ( 1 FDA reports)
CATHETER RELATED INFECTION ( 1 FDA reports)
CD4 LYMPHOCYTES ABNORMAL ( 1 FDA reports)
CD4 LYMPHOCYTES DECREASED ( 1 FDA reports)
CD8 LYMPHOCYTES DECREASED ( 1 FDA reports)
CENTRAL PONTINE MYELINOLYSIS ( 1 FDA reports)
CEREBELLAR SYNDROME ( 1 FDA reports)
CEREBRAL ARTERY OCCLUSION ( 1 FDA reports)
CEREBRAL HAEMATOMA ( 1 FDA reports)
CEREBRAL SMALL VESSEL ISCHAEMIC DISEASE ( 1 FDA reports)
CEREBRAL TOXOPLASMOSIS ( 1 FDA reports)
CERVICAL DISCHARGE ( 1 FDA reports)
CERVICOBRACHIAL SYNDROME ( 1 FDA reports)
CERVIX DISORDER ( 1 FDA reports)
CHAPPED LIPS ( 1 FDA reports)
CIRCADIAN RHYTHM SLEEP DISORDER ( 1 FDA reports)
CLOSTRIDIUM DIFFICILE TOXIN TEST POSITIVE ( 1 FDA reports)
COLITIS COLLAGENOUS ( 1 FDA reports)
COLLAPSE OF LUNG ( 1 FDA reports)
COLORECTAL CANCER METASTATIC ( 1 FDA reports)
COLOSTOMY ( 1 FDA reports)
COMMUNICATION DISORDER ( 1 FDA reports)
COMPUTERISED TOMOGRAM ABDOMEN ABNORMAL ( 1 FDA reports)
CONDUCTION DISORDER ( 1 FDA reports)
CONFUSIONAL AROUSAL ( 1 FDA reports)
CONJUNCTIVAL HYPERAEMIA ( 1 FDA reports)
CONTACT LENS COMPLICATION ( 1 FDA reports)
CORNEAL GRAFT REJECTION ( 1 FDA reports)
COXSACKIE VIRAL INFECTION ( 1 FDA reports)
CREST SYNDROME ( 1 FDA reports)
CRYPTOGENIC ORGANIZING PNEUMONIA ( 1 FDA reports)
CULTURE URINE POSITIVE ( 1 FDA reports)
CUSHINGOID ( 1 FDA reports)
CUTANEOUS TUBERCULOSIS ( 1 FDA reports)
DANDRUFF ( 1 FDA reports)
DEAFNESS UNILATERAL ( 1 FDA reports)
DEGENERATION OF UTERINE LEIOMYOMA ( 1 FDA reports)
DEJA VU ( 1 FDA reports)
DEMENTIA ALZHEIMER'S TYPE ( 1 FDA reports)
DENTAL EXAMINATION ( 1 FDA reports)
DENTAL EXAMINATION ABNORMAL ( 1 FDA reports)
DEPENDENCE ON ENABLING MACHINE OR DEVICE ( 1 FDA reports)
DERMATITIS HERPETIFORMIS ( 1 FDA reports)
DIABETIC KETOACIDOSIS ( 1 FDA reports)
DISLOCATION OF VERTEBRA ( 1 FDA reports)
DIVERTICULAR PERFORATION ( 1 FDA reports)
DIZZINESS POSTURAL ( 1 FDA reports)
DROOLING ( 1 FDA reports)
DRUG ERUPTION ( 1 FDA reports)
DRUG INTERACTION INHIBITION ( 1 FDA reports)
DRUG LEVEL BELOW THERAPEUTIC ( 1 FDA reports)
DRUG-INDUCED LIVER INJURY ( 1 FDA reports)
DUODENAL ULCER PERFORATION ( 1 FDA reports)
DYSGRAPHIA ( 1 FDA reports)
DYSLALIA ( 1 FDA reports)
DYSPNOEA AT REST ( 1 FDA reports)
EAR INFECTION ( 1 FDA reports)
EAR INFECTION VIRAL ( 1 FDA reports)
EARLY SATIETY ( 1 FDA reports)
ECZEMA INFECTED ( 1 FDA reports)
ELECTROCARDIOGRAM PR PROLONGATION ( 1 FDA reports)
ELECTROCARDIOGRAM REPOLARISATION ABNORMALITY ( 1 FDA reports)
ELECTROCARDIOGRAM ST SEGMENT DEPRESSION ( 1 FDA reports)
ELECTROCARDIOGRAM T WAVE ABNORMAL ( 1 FDA reports)
ELECTROLYTE IMBALANCE ( 1 FDA reports)
ELECTROMECHANICAL DISSOCIATION ( 1 FDA reports)
EMBOLIC STROKE ( 1 FDA reports)
ENAMEL ANOMALY ( 1 FDA reports)
ENCEPHALITIS VIRAL ( 1 FDA reports)
ENDOMETRIAL CANCER STAGE III ( 1 FDA reports)
ENLARGED CLITORIS ( 1 FDA reports)
ENTEROBACTER INFECTION ( 1 FDA reports)
ENTEROBACTER SEPSIS ( 1 FDA reports)
ENURESIS ( 1 FDA reports)
ENZYME ABNORMALITY ( 1 FDA reports)
EPIGASTRIC DISCOMFORT ( 1 FDA reports)
EXANTHEM ( 1 FDA reports)
EXERCISE ELECTROCARDIOGRAM ABNORMAL ( 1 FDA reports)
EXERCISE LACK OF ( 1 FDA reports)
EXTRADURAL HAEMATOMA ( 1 FDA reports)
EYE DEGENERATIVE DISORDER ( 1 FDA reports)
EYE OPERATION ( 1 FDA reports)
EYE REDNESS ( 1 FDA reports)
EYELID DISORDER ( 1 FDA reports)
FACIAL WASTING ( 1 FDA reports)
FEBRILE INFECTION ( 1 FDA reports)
FOETOR HEPATICUS ( 1 FDA reports)
FOOD ALLERGY ( 1 FDA reports)
FORAMINOTOMY ( 1 FDA reports)
FORMICATION ( 1 FDA reports)
FRACTURE DELAYED UNION ( 1 FDA reports)
FUNGAL SKIN INFECTION ( 1 FDA reports)
FUNGUS SPUTUM TEST POSITIVE ( 1 FDA reports)
GALACTORRHOEA ( 1 FDA reports)
GALLBLADDER OPERATION ( 1 FDA reports)
GASTRIC MUCOSAL LESION ( 1 FDA reports)
GASTRITIS ATROPHIC ( 1 FDA reports)
GASTROINTESTINAL HYPERMOTILITY ( 1 FDA reports)
GASTROINTESTINAL INFECTION ( 1 FDA reports)
GASTROINTESTINAL PERFORATION ( 1 FDA reports)
GENERAL SYMPTOM ( 1 FDA reports)
GENITAL DISORDER FEMALE ( 1 FDA reports)
GENITAL PROLAPSE ( 1 FDA reports)
GINGIVAL EROSION ( 1 FDA reports)
GINGIVITIS ULCERATIVE ( 1 FDA reports)
GLOBULINS DECREASED ( 1 FDA reports)
GLOBULINS INCREASED ( 1 FDA reports)
GLOMERULAR FILTRATION RATE DECREASED ( 1 FDA reports)
GOUTY ARTHRITIS ( 1 FDA reports)
GRAFT INFECTION ( 1 FDA reports)
GRANULOMA SKIN ( 1 FDA reports)
GRANULOMATOUS PNEUMONITIS ( 1 FDA reports)
GRIP STRENGTH DECREASED ( 1 FDA reports)
HAEMATOMA INFECTION ( 1 FDA reports)
HAIR COLOUR CHANGES ( 1 FDA reports)
HALLUCINATION, AUDITORY ( 1 FDA reports)
HELICOBACTER INFECTION ( 1 FDA reports)
HENOCH-SCHONLEIN PURPURA ( 1 FDA reports)
HEPATIC CANCER METASTATIC ( 1 FDA reports)
HEPATIC HAEMATOMA ( 1 FDA reports)
HEPATITIS B ( 1 FDA reports)
HEPATITIS C RNA INCREASED ( 1 FDA reports)
HEPATOSPLENOMEGALY ( 1 FDA reports)
HERNIA REPAIR ( 1 FDA reports)
HODGKIN'S DISEASE ( 1 FDA reports)
HOSPITALISATION ( 1 FDA reports)
HUNGER ( 1 FDA reports)
HYPERACUSIS ( 1 FDA reports)
HYPERCREATININAEMIA ( 1 FDA reports)
HYPEREOSINOPHILIC SYNDROME ( 1 FDA reports)
HYPERPHOSPHATASAEMIA ( 1 FDA reports)
HYPERVENTILATION ( 1 FDA reports)
HYPOPHOSPHATAEMIA ( 1 FDA reports)
HYPOREFLEXIA ( 1 FDA reports)
HYPOTHERMIA ( 1 FDA reports)
ILIUM FRACTURE ( 1 FDA reports)
IMPATIENCE ( 1 FDA reports)
INAPPROPRIATE ANTIDIURETIC HORMONE SECRETION ( 1 FDA reports)
INCISION SITE PAIN ( 1 FDA reports)
INCOHERENT ( 1 FDA reports)
INCORRECT DOSE ADMINISTERED BY DEVICE ( 1 FDA reports)
INCORRECT STORAGE OF DRUG ( 1 FDA reports)
INCREASED TENDENCY TO BRUISE ( 1 FDA reports)
INDURATION ( 1 FDA reports)
INFECTED SKIN ULCER ( 1 FDA reports)
INFLAMMATORY MARKER INCREASED ( 1 FDA reports)
INJECTION SITE BRUISING ( 1 FDA reports)
INJECTION SITE HAEMATOMA ( 1 FDA reports)
INJECTION SITE REACTION ( 1 FDA reports)
INJECTION SITE VESICLES ( 1 FDA reports)
INTENTIONAL OVERDOSE ( 1 FDA reports)
INTERNAL FIXATION OF FRACTURE ( 1 FDA reports)
INTERNATIONAL NORMALISED RATIO ABNORMAL ( 1 FDA reports)
INTERNATIONAL NORMALISED RATIO FLUCTUATION ( 1 FDA reports)
INTERVERTEBRAL DISC COMPRESSION ( 1 FDA reports)
INTESTINAL ADENOCARCINOMA ( 1 FDA reports)
INTRA-ABDOMINAL HAEMATOMA ( 1 FDA reports)
INTRACRANIAL PRESSURE INCREASED ( 1 FDA reports)
INTRAVENTRICULAR HAEMORRHAGE ( 1 FDA reports)
INTUBATION ( 1 FDA reports)
INTUBATION COMPLICATION ( 1 FDA reports)
IRRITABILITY ( 1 FDA reports)
JAUNDICE CHOLESTATIC ( 1 FDA reports)
JOINT CONTRACTURE ( 1 FDA reports)
JOINT DESTRUCTION ( 1 FDA reports)
JOINT LOCK ( 1 FDA reports)
JOINT WARMTH ( 1 FDA reports)
KLEBSIELLA BACTERAEMIA ( 1 FDA reports)
LABYRINTHITIS ( 1 FDA reports)
LACTIC ACIDOSIS ( 1 FDA reports)
LARGE INTESTINAL HAEMORRHAGE ( 1 FDA reports)
LASER THERAPY ( 1 FDA reports)
LEUKOCYTOCLASTIC VASCULITIS ( 1 FDA reports)
LIBIDO DISORDER ( 1 FDA reports)
LIP OEDEMA ( 1 FDA reports)
LIPOPROTEIN (A) INCREASED ( 1 FDA reports)
LOCAL ANAESTHESIA ( 1 FDA reports)
LOSS OF CONTROL OF LEGS ( 1 FDA reports)
LOWER RESPIRATORY TRACT INFECTION ( 1 FDA reports)
LYMPH NODE PAIN ( 1 FDA reports)
LYMPHOCYTE COUNT INCREASED ( 1 FDA reports)
MADAROSIS ( 1 FDA reports)
MALIGNANT HYPERTENSION ( 1 FDA reports)
MAMMOGRAM ABNORMAL ( 1 FDA reports)
MANDIBULECTOMY ( 1 FDA reports)
MASTITIS ( 1 FDA reports)
MECHANICAL COMPLICATION OF IMPLANT ( 1 FDA reports)
MEDIASTINAL DISORDER ( 1 FDA reports)
MEDULLOBLASTOMA ( 1 FDA reports)
MENSTRUATION IRREGULAR ( 1 FDA reports)
MESENTERIC ARTERY THROMBOSIS ( 1 FDA reports)
METABOLIC DISORDER ( 1 FDA reports)
METABOLIC ENCEPHALOPATHY ( 1 FDA reports)
METASTASES TO LARGE INTESTINE ( 1 FDA reports)
METASTASES TO PERIPHERAL VASCULAR SYSTEM ( 1 FDA reports)
METASTASES TO URINARY TRACT ( 1 FDA reports)
MICROANGIOPATHY ( 1 FDA reports)
MORBID THOUGHTS ( 1 FDA reports)
MORTON'S NEUROMA ( 1 FDA reports)
MOTOR DYSFUNCTION ( 1 FDA reports)
MOUTH INJURY ( 1 FDA reports)
MULTIPLE CHEMICAL SENSITIVITY ( 1 FDA reports)
MULTIPLE DRUG OVERDOSE INTENTIONAL ( 1 FDA reports)
MULTIPLE FRACTURES ( 1 FDA reports)
MUSCLE ATROPHY ( 1 FDA reports)
MUSCLE CRAMP ( 1 FDA reports)
MYASTHENIA GRAVIS ( 1 FDA reports)
NAIL INFECTION ( 1 FDA reports)
NASAL CAVITY CANCER ( 1 FDA reports)
NEOPLASM RECURRENCE ( 1 FDA reports)
NEPHRECTOMY ( 1 FDA reports)
NEPHRITIS INTERSTITIAL ( 1 FDA reports)
NERVE ROOT COMPRESSION ( 1 FDA reports)
NEUROLYSIS ( 1 FDA reports)
NEUROMA ( 1 FDA reports)
NEUROSIS ( 1 FDA reports)
NIPPLE DISORDER ( 1 FDA reports)
NO ADVERSE DRUG EFFECT ( 1 FDA reports)
NO ADVERSE EFFECT ( 1 FDA reports)
NO ADVERSE REACTION ( 1 FDA reports)
NON-CARDIAC CHEST PAIN ( 1 FDA reports)
NON-HODGKIN'S LYMPHOMA ( 1 FDA reports)
NONSPECIFIC REACTION ( 1 FDA reports)
NORMAL TENSION GLAUCOMA ( 1 FDA reports)
OBSTRUCTION GASTRIC ( 1 FDA reports)
OESOPHAGEAL ULCER HAEMORRHAGE ( 1 FDA reports)
OESOPHAGITIS HAEMORRHAGIC ( 1 FDA reports)
OOPHORECTOMY BILATERAL ( 1 FDA reports)
OPTIC NERVE DISORDER ( 1 FDA reports)
OSTEOCHONDROSIS ( 1 FDA reports)
OSTEOTOMY ( 1 FDA reports)
PAIN EXACERBATED ( 1 FDA reports)
PANCREATIC ATROPHY ( 1 FDA reports)
PANCREATIC DUCT OBSTRUCTION ( 1 FDA reports)
PAPILLARY MUSCLE DISORDER ( 1 FDA reports)
PARATHYROID DISORDER ( 1 FDA reports)
PARATHYROID TUMOUR BENIGN ( 1 FDA reports)
PARATRACHEAL LYMPHADENOPATHY ( 1 FDA reports)
PARESIS ( 1 FDA reports)
PARKINSON'S DISEASE ( 1 FDA reports)
PCO2 INCREASED ( 1 FDA reports)
PEPTIC ULCER HAEMORRHAGE ( 1 FDA reports)
PEPTOSTREPTOCOCCUS INFECTION ( 1 FDA reports)
PERICARDIAL EFFUSION MALIGNANT ( 1 FDA reports)
PERIPHERAL EMBOLISM ( 1 FDA reports)
PERITONITIS ( 1 FDA reports)
PIRIFORMIS SYNDROME ( 1 FDA reports)
PITTING OEDEMA ( 1 FDA reports)
PITYRIASIS ( 1 FDA reports)
PLASMAPHERESIS ( 1 FDA reports)
PLEURAL HAEMORRHAGE ( 1 FDA reports)
PLEURITIC PAIN ( 1 FDA reports)
PNEUMOCOCCAL INFECTION ( 1 FDA reports)
PNEUMONIA PRIMARY ATYPICAL ( 1 FDA reports)
POLYPECTOMY ( 1 FDA reports)
POST-TRAUMATIC STRESS DISORDER ( 1 FDA reports)
POSTOPERATIVE FEVER ( 1 FDA reports)
POSTOPERATIVE INFECTION ( 1 FDA reports)
PRURIGO ( 1 FDA reports)
PSYCHIATRIC SYMPTOM ( 1 FDA reports)
PSYCHOMOTOR RETARDATION ( 1 FDA reports)
PULMONARY THROMBOSIS ( 1 FDA reports)
PULSE ABNORMAL ( 1 FDA reports)
PUNCTATE KERATITIS ( 1 FDA reports)
PUPILLARY DISORDER ( 1 FDA reports)
PYELONEPHRITIS ( 1 FDA reports)
QUALITY OF LIFE DECREASED ( 1 FDA reports)
RADIATION ASSOCIATED PAIN ( 1 FDA reports)
RADIATION PNEUMONITIS ( 1 FDA reports)
RECTAL CANCER ( 1 FDA reports)
RECTAL DISCHARGE ( 1 FDA reports)
RECTOCELE REPAIR ( 1 FDA reports)
RENAL ARTERY OCCLUSION ( 1 FDA reports)
RENAL ARTERY STENOSIS ( 1 FDA reports)
RENAL COLIC ( 1 FDA reports)
RENAL PAIN ( 1 FDA reports)
RENAL TUBULAR NECROSIS ( 1 FDA reports)
RESPIRATORY DEPRESSION ( 1 FDA reports)
RESPIRATORY RATE INCREASED ( 1 FDA reports)
RESPIRATORY TRACT HAEMORRHAGE ( 1 FDA reports)
RESUSCITATION ( 1 FDA reports)
RETINAL ARTERY OCCLUSION ( 1 FDA reports)
RETINAL EXUDATES ( 1 FDA reports)
RETINAL VEIN THROMBOSIS ( 1 FDA reports)
RETINOPATHY ( 1 FDA reports)
RETINOPATHY HYPERTENSIVE ( 1 FDA reports)
SARCOMA OF SKIN ( 1 FDA reports)
SCLERITIS ( 1 FDA reports)
SICK SINUS SYNDROME ( 1 FDA reports)
SIMPLEX VIRUS TEST POSITIVE ( 1 FDA reports)
SKIN CHAPPED ( 1 FDA reports)
SKIN DESQUAMATION ( 1 FDA reports)
SKIN FRAGILITY ( 1 FDA reports)
SKIN TIGHTNESS ( 1 FDA reports)
SKULL FRACTURE ( 1 FDA reports)
SMALL INTESTINE CARCINOMA ( 1 FDA reports)
SPINAL PAIN ( 1 FDA reports)
SPLENIC CALCIFICATION ( 1 FDA reports)
STOOL ANALYSIS ABNORMAL ( 1 FDA reports)
STRESS URINARY INCONTINENCE ( 1 FDA reports)
STUPOR ( 1 FDA reports)
SUBCLAVIAN ARTERY STENOSIS ( 1 FDA reports)
SUBCUTANEOUS ABSCESS ( 1 FDA reports)
SUDDEN CARDIAC DEATH ( 1 FDA reports)
SURGICAL PROCEDURE REPEATED ( 1 FDA reports)
SYNCOPE VASOVAGAL ( 1 FDA reports)
SYNOVIAL FLUID CRYSTAL ( 1 FDA reports)
T-LYMPHOCYTE COUNT ABNORMAL ( 1 FDA reports)
T-LYMPHOCYTE COUNT DECREASED ( 1 FDA reports)
TACHYPHRENIA ( 1 FDA reports)
TACHYPNOEA ( 1 FDA reports)
TEARFULNESS ( 1 FDA reports)
TENDON PAIN ( 1 FDA reports)
THERAPEUTIC RESPONSE UNEXPECTED ( 1 FDA reports)
THERAPEUTIC RESPONSE UNEXPECTED WITH DRUG SUBSTITUTION ( 1 FDA reports)
THROMBOCYTHAEMIA ( 1 FDA reports)
THROMBOSIS MESENTERIC VESSEL ( 1 FDA reports)
THYROID MASS ( 1 FDA reports)
THYROXINE DECREASED ( 1 FDA reports)
TONSILLECTOMY ( 1 FDA reports)
TOOTH ANKYLOSIS ( 1 FDA reports)
TOOTH EROSION ( 1 FDA reports)
TOXIC NODULAR GOITRE ( 1 FDA reports)
TRAUMATIC ARTHRITIS ( 1 FDA reports)
TREATMENT FAILURE ( 1 FDA reports)
TRI-IODOTHYRONINE UPTAKE DECREASED ( 1 FDA reports)
TRICHOTILLOMANIA ( 1 FDA reports)
TROPONIN INCREASED ( 1 FDA reports)
TUMOUR EMBOLISM ( 1 FDA reports)
TUMOUR HAEMORRHAGE ( 1 FDA reports)
UNDERDOSE ( 1 FDA reports)
UPPER GASTROINTESTINAL HAEMORRHAGE ( 1 FDA reports)
URETHRAL DISCHARGE ( 1 FDA reports)
URGE INCONTINENCE ( 1 FDA reports)
URINARY TRACT DISORDER ( 1 FDA reports)
URINE OUTPUT INCREASED ( 1 FDA reports)
URINE POTASSIUM INCREASED ( 1 FDA reports)
UTERINE ENLARGEMENT ( 1 FDA reports)
UVULITIS ( 1 FDA reports)
VAGINAL DISORDER ( 1 FDA reports)
VAGINAL LESION ( 1 FDA reports)
VANISHING BILE DUCT SYNDROME ( 1 FDA reports)
VARICOSE VEIN RUPTURED ( 1 FDA reports)
VASCULAR CAUTERISATION ( 1 FDA reports)
VASCULITIS ( 1 FDA reports)
VENIPUNCTURE SITE THROMBOSIS ( 1 FDA reports)
VENTRICULAR FIBRILLATION ( 1 FDA reports)
VITAMIN B12 INCREASED ( 1 FDA reports)
VITREOUS ADHESIONS ( 1 FDA reports)
VOCAL CORD ATROPHY ( 1 FDA reports)
WRONG DRUG ADMINISTERED ( 1 FDA reports)
X-RAY DENTAL ( 1 FDA reports)

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