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

PAIN ( 244 FDA reports)
NAUSEA ( 236 FDA reports)
DIARRHOEA ( 221 FDA reports)
DEATH ( 217 FDA reports)
ANAEMIA ( 216 FDA reports)
WHITE BLOOD CELL COUNT DECREASED ( 190 FDA reports)
FATIGUE ( 187 FDA reports)
ANXIETY ( 181 FDA reports)
PYREXIA ( 176 FDA reports)
PLEURAL EFFUSION ( 172 FDA reports)
DYSPNOEA ( 165 FDA reports)
OSTEONECROSIS OF JAW ( 163 FDA reports)
NEUTROPENIA ( 161 FDA reports)
DEHYDRATION ( 159 FDA reports)
NEUROPATHY PERIPHERAL ( 153 FDA reports)
VOMITING ( 151 FDA reports)
METASTASES TO BONE ( 149 FDA reports)
BONE DISORDER ( 144 FDA reports)
OSTEOMYELITIS ( 143 FDA reports)
PNEUMONIA ( 136 FDA reports)
ASTHENIA ( 133 FDA reports)
NEUTROPHIL COUNT DECREASED ( 132 FDA reports)
DECREASED APPETITE ( 131 FDA reports)
BACK PAIN ( 117 FDA reports)
ABDOMINAL PAIN ( 116 FDA reports)
METASTASES TO LIVER ( 114 FDA reports)
FEBRILE NEUTROPENIA ( 112 FDA reports)
GENERAL PHYSICAL HEALTH DETERIORATION ( 107 FDA reports)
SEPSIS ( 107 FDA reports)
PAIN IN JAW ( 104 FDA reports)
DEPRESSION ( 103 FDA reports)
INFECTION ( 101 FDA reports)
EMOTIONAL DISTRESS ( 98 FDA reports)
HAEMOGLOBIN DECREASED ( 98 FDA reports)
ARTHRALGIA ( 97 FDA reports)
STOMATITIS ( 97 FDA reports)
ALOPECIA ( 96 FDA reports)
MUCOSAL INFLAMMATION ( 96 FDA reports)
INJURY ( 94 FDA reports)
METASTASES TO CENTRAL NERVOUS SYSTEM ( 94 FDA reports)
ATELECTASIS ( 92 FDA reports)
CONSTIPATION ( 91 FDA reports)
BONE PAIN ( 89 FDA reports)
OSTEONECROSIS ( 89 FDA reports)
THROMBOCYTOPENIA ( 88 FDA reports)
METASTASES TO SPINE ( 86 FDA reports)
WEIGHT DECREASED ( 86 FDA reports)
CELLULITIS ( 85 FDA reports)
DENTAL CARIES ( 85 FDA reports)
METASTASES TO LUNG ( 85 FDA reports)
HEADACHE ( 84 FDA reports)
OEDEMA PERIPHERAL ( 81 FDA reports)
ANHEDONIA ( 80 FDA reports)
ASCITES ( 79 FDA reports)
BREAST CANCER METASTATIC ( 78 FDA reports)
CHEST PAIN ( 77 FDA reports)
GASTROOESOPHAGEAL REFLUX DISEASE ( 77 FDA reports)
CONFUSIONAL STATE ( 76 FDA reports)
TOOTH EXTRACTION ( 75 FDA reports)
PLATELET COUNT DECREASED ( 74 FDA reports)
SYNCOPE ( 74 FDA reports)
DEFORMITY ( 73 FDA reports)
OSTEOARTHRITIS ( 70 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 69 FDA reports)
GAIT DISTURBANCE ( 68 FDA reports)
HYPOPHAGIA ( 68 FDA reports)
MYALGIA ( 68 FDA reports)
BONE LESION ( 67 FDA reports)
HYPERTENSION ( 67 FDA reports)
SPINAL OSTEOARTHRITIS ( 66 FDA reports)
TACHYCARDIA ( 66 FDA reports)
HYPOTENSION ( 65 FDA reports)
IMPAIRED HEALING ( 65 FDA reports)
PARAESTHESIA ( 65 FDA reports)
DEEP VEIN THROMBOSIS ( 64 FDA reports)
HYPOAESTHESIA ( 64 FDA reports)
BRONCHITIS ( 63 FDA reports)
DYSPHAGIA ( 63 FDA reports)
BLOOD ALKALINE PHOSPHATASE INCREASED ( 62 FDA reports)
RASH ( 62 FDA reports)
RENAL FAILURE ACUTE ( 62 FDA reports)
DIZZINESS ( 61 FDA reports)
PURULENT DISCHARGE ( 61 FDA reports)
DISEASE PROGRESSION ( 59 FDA reports)
NEOPLASM MALIGNANT ( 59 FDA reports)
CHILLS ( 57 FDA reports)
DECREASED INTEREST ( 57 FDA reports)
ORAL CANDIDIASIS ( 57 FDA reports)
SWELLING ( 57 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 56 FDA reports)
FALL ( 56 FDA reports)
ORAL PAIN ( 56 FDA reports)
OSTEOPENIA ( 56 FDA reports)
CARDIAC FAILURE CONGESTIVE ( 53 FDA reports)
DYSURIA ( 51 FDA reports)
HYPOKALAEMIA ( 51 FDA reports)
MALIGNANT NEOPLASM PROGRESSION ( 51 FDA reports)
URINARY TRACT INFECTION ( 51 FDA reports)
VISION BLURRED ( 51 FDA reports)
HEPATIC STEATOSIS ( 50 FDA reports)
INTERVERTEBRAL DISC PROTRUSION ( 50 FDA reports)
TOOTH LOSS ( 50 FDA reports)
UPPER RESPIRATORY TRACT INFECTION ( 50 FDA reports)
CHRONIC OBSTRUCTIVE PULMONARY DISEASE ( 49 FDA reports)
CHRONIC SINUSITIS ( 48 FDA reports)
CYST ( 48 FDA reports)
LUNG NEOPLASM ( 48 FDA reports)
PAIN IN EXTREMITY ( 47 FDA reports)
COUGH ( 46 FDA reports)
C-REACTIVE PROTEIN INCREASED ( 45 FDA reports)
PULMONARY EMBOLISM ( 45 FDA reports)
EPISTAXIS ( 44 FDA reports)
ERYTHEMA ( 44 FDA reports)
HAEMORRHOIDS ( 44 FDA reports)
LOSS OF CONSCIOUSNESS ( 44 FDA reports)
MACULAR OEDEMA ( 44 FDA reports)
MUSCULAR WEAKNESS ( 44 FDA reports)
HEART RATE INCREASED ( 43 FDA reports)
MALAISE ( 43 FDA reports)
INTERSTITIAL LUNG DISEASE ( 42 FDA reports)
OEDEMA ( 42 FDA reports)
GASTRITIS ( 41 FDA reports)
HYDRONEPHROSIS ( 41 FDA reports)
RENAL CYST ( 41 FDA reports)
DYSGEUSIA ( 40 FDA reports)
HEPATIC CYST ( 40 FDA reports)
JAW FRACTURE ( 40 FDA reports)
LOOSE TOOTH ( 40 FDA reports)
PANCYTOPENIA ( 39 FDA reports)
TRICUSPID VALVE INCOMPETENCE ( 39 FDA reports)
UNRESPONSIVE TO STIMULI ( 39 FDA reports)
GINGIVITIS ( 38 FDA reports)
PRIMARY SEQUESTRUM ( 38 FDA reports)
BLOOD GLUCOSE INCREASED ( 37 FDA reports)
BREAST CANCER RECURRENT ( 37 FDA reports)
CONVULSION ( 37 FDA reports)
MASS ( 37 FDA reports)
DEVICE RELATED INFECTION ( 36 FDA reports)
DISCOMFORT ( 36 FDA reports)
EAR PAIN ( 36 FDA reports)
LEUKOPENIA ( 36 FDA reports)
MENTAL STATUS CHANGES ( 36 FDA reports)
NEOPLASM PROGRESSION ( 36 FDA reports)
PERICARDIAL EFFUSION ( 36 FDA reports)
SPINAL COMPRESSION FRACTURE ( 36 FDA reports)
TOOTH ABSCESS ( 36 FDA reports)
FISTULA ( 35 FDA reports)
HERPES SIMPLEX ( 35 FDA reports)
INSOMNIA ( 35 FDA reports)
MALIGNANT PLEURAL EFFUSION ( 35 FDA reports)
NECK PAIN ( 34 FDA reports)
ONYCHOMYCOSIS ( 34 FDA reports)
SPONDYLOLISTHESIS ( 34 FDA reports)
TOOTHACHE ( 34 FDA reports)
BLOOD BILIRUBIN INCREASED ( 33 FDA reports)
BLOOD CREATININE INCREASED ( 33 FDA reports)
TREMOR ( 33 FDA reports)
WHEELCHAIR USER ( 33 FDA reports)
ASPIRATION PLEURAL CAVITY ( 32 FDA reports)
CARDIOMEGALY ( 32 FDA reports)
EXPOSED BONE IN JAW ( 32 FDA reports)
HIATUS HERNIA ( 32 FDA reports)
INFLAMMATION ( 32 FDA reports)
PATHOLOGICAL FRACTURE ( 32 FDA reports)
PNEUMOTHORAX ( 32 FDA reports)
DECUBITUS ULCER ( 31 FDA reports)
HYPONATRAEMIA ( 31 FDA reports)
RIB FRACTURE ( 31 FDA reports)
ATRIAL FIBRILLATION ( 30 FDA reports)
HEPATIC FUNCTION ABNORMAL ( 30 FDA reports)
ORAL DISORDER ( 30 FDA reports)
OSTEOSCLEROSIS ( 30 FDA reports)
PERIPHERAL SENSORY NEUROPATHY ( 30 FDA reports)
SEPTIC SHOCK ( 30 FDA reports)
URINARY RETENTION ( 30 FDA reports)
AORTIC ARTERIOSCLEROSIS ( 29 FDA reports)
BREAST CANCER ( 29 FDA reports)
DRY MOUTH ( 29 FDA reports)
DYSPEPSIA ( 29 FDA reports)
HYPOXIA ( 29 FDA reports)
LUNG INFILTRATION ( 29 FDA reports)
SINUS DISORDER ( 29 FDA reports)
SWELLING FACE ( 29 FDA reports)
COLITIS ( 28 FDA reports)
DYSPNOEA EXERTIONAL ( 28 FDA reports)
EJECTION FRACTION DECREASED ( 28 FDA reports)
MUSCULOSKELETAL PAIN ( 28 FDA reports)
PNEUMONITIS ( 28 FDA reports)
UTERINE LEIOMYOMA ( 28 FDA reports)
CENTRAL VENOUS CATHETERISATION ( 27 FDA reports)
HYPERKALAEMIA ( 27 FDA reports)
LIFE EXPECTANCY SHORTENED ( 27 FDA reports)
SKIN LESION ( 27 FDA reports)
ABSCESS ( 26 FDA reports)
ENDODONTIC PROCEDURE ( 26 FDA reports)
GAMMA-GLUTAMYLTRANSFERASE INCREASED ( 26 FDA reports)
HEPATIC CIRRHOSIS ( 26 FDA reports)
LACRIMATION INCREASED ( 26 FDA reports)
METASTATIC NEOPLASM ( 26 FDA reports)
RENAL FAILURE ( 26 FDA reports)
DYSPHONIA ( 25 FDA reports)
GASTROINTESTINAL HAEMORRHAGE ( 25 FDA reports)
LEUKOCYTOSIS ( 25 FDA reports)
LYMPHADENOPATHY ( 25 FDA reports)
MASTICATION DISORDER ( 25 FDA reports)
NAIL DISORDER ( 25 FDA reports)
OSTEOPOROSIS ( 25 FDA reports)
PALMAR-PLANTAR ERYTHRODYSAESTHESIA SYNDROME ( 25 FDA reports)
RESPIRATORY FAILURE ( 25 FDA reports)
SUBCUTANEOUS ABSCESS ( 25 FDA reports)
BLINDNESS UNILATERAL ( 24 FDA reports)
DEBRIDEMENT ( 24 FDA reports)
GINGIVAL BLEEDING ( 24 FDA reports)
HERPES ZOSTER ( 24 FDA reports)
MITRAL VALVE INCOMPETENCE ( 24 FDA reports)
MUSCLE SPASMS ( 24 FDA reports)
NEPHROLITHIASIS ( 24 FDA reports)
PRURITUS ( 24 FDA reports)
RHINORRHOEA ( 24 FDA reports)
SINUSITIS ( 24 FDA reports)
DISABILITY ( 23 FDA reports)
FACIAL PALSY ( 23 FDA reports)
LETHARGY ( 23 FDA reports)
LUMBAR SPINAL STENOSIS ( 23 FDA reports)
NIGHT SWEATS ( 23 FDA reports)
OESOPHAGITIS ( 23 FDA reports)
TENDERNESS ( 23 FDA reports)
TOOTH DISORDER ( 23 FDA reports)
WALKING AID USER ( 23 FDA reports)
CHEST DISCOMFORT ( 22 FDA reports)
GINGIVAL SWELLING ( 22 FDA reports)
HEPATIC FAILURE ( 22 FDA reports)
INTERVERTEBRAL DISC DEGENERATION ( 22 FDA reports)
LUNG NEOPLASM MALIGNANT ( 22 FDA reports)
LYMPHADENOPATHY MEDIASTINAL ( 22 FDA reports)
SCOLIOSIS ( 22 FDA reports)
THROAT IRRITATION ( 22 FDA reports)
ABDOMINAL DISTENSION ( 21 FDA reports)
BURSITIS ( 21 FDA reports)
DIABETES MELLITUS ( 21 FDA reports)
DRY EYE ( 21 FDA reports)
HAEMATOCRIT DECREASED ( 21 FDA reports)
HALLUCINATION ( 21 FDA reports)
HEPATOMEGALY ( 21 FDA reports)
MENINGITIS ( 21 FDA reports)
SEQUESTRECTOMY ( 21 FDA reports)
SPLENOMEGALY ( 21 FDA reports)
VAGINAL INFECTION ( 21 FDA reports)
ARTHRITIS ( 20 FDA reports)
DYSKINESIA ( 20 FDA reports)
GINGIVAL PAIN ( 20 FDA reports)
HYPERSENSITIVITY ( 20 FDA reports)
OPEN WOUND ( 20 FDA reports)
OSTEORADIONECROSIS ( 20 FDA reports)
PERIODONTITIS ( 20 FDA reports)
PULMONARY FIBROSIS ( 20 FDA reports)
SOMNOLENCE ( 20 FDA reports)
THROMBOPHLEBITIS ( 20 FDA reports)
VOCAL CORD PARALYSIS ( 20 FDA reports)
ASTHMA ( 19 FDA reports)
BACTERIAL INFECTION ( 19 FDA reports)
BLOOD URINE PRESENT ( 19 FDA reports)
DIPLOPIA ( 19 FDA reports)
KYPHOSIS ( 19 FDA reports)
LYMPHOEDEMA ( 19 FDA reports)
NEUROGENIC BLADDER ( 19 FDA reports)
OTITIS MEDIA ( 19 FDA reports)
PALPITATIONS ( 19 FDA reports)
SPINAL COLUMN STENOSIS ( 19 FDA reports)
TRISMUS ( 19 FDA reports)
VAGINAL HAEMORRHAGE ( 19 FDA reports)
BLOOD SODIUM DECREASED ( 18 FDA reports)
BONE DEBRIDEMENT ( 18 FDA reports)
BREATH ODOUR ( 18 FDA reports)
COMPRESSION FRACTURE ( 18 FDA reports)
CYSTITIS HAEMORRHAGIC ( 18 FDA reports)
EXTERNAL EAR DISORDER ( 18 FDA reports)
FOOT FRACTURE ( 18 FDA reports)
HYPOCALCAEMIA ( 18 FDA reports)
LIVER FUNCTION TEST ABNORMAL ( 18 FDA reports)
METASTASES TO LYMPH NODES ( 18 FDA reports)
MYOSITIS ( 18 FDA reports)
PERICARDIAL DISEASE ( 18 FDA reports)
SINUS TACHYCARDIA ( 18 FDA reports)
SMALL INTESTINAL OBSTRUCTION ( 18 FDA reports)
SQUAMOUS CELL CARCINOMA ( 18 FDA reports)
TOOTH INFECTION ( 18 FDA reports)
WHITE BLOOD CELL COUNT INCREASED ( 18 FDA reports)
ABSCESS JAW ( 17 FDA reports)
ADRENAL MASS ( 17 FDA reports)
APPENDICITIS ( 17 FDA reports)
BODY TEMPERATURE INCREASED ( 17 FDA reports)
CANDIDIASIS ( 17 FDA reports)
CLOSTRIDIUM DIFFICILE COLITIS ( 17 FDA reports)
DEPRESSED LEVEL OF CONSCIOUSNESS ( 17 FDA reports)
HYPOTHYROIDISM ( 17 FDA reports)
LIVER DISORDER ( 17 FDA reports)
LUNG DISORDER ( 17 FDA reports)
PANCREATIC CARCINOMA ( 17 FDA reports)
VERTEBROPLASTY ( 17 FDA reports)
AORTIC VALVE INCOMPETENCE ( 16 FDA reports)
APPENDICITIS PERFORATED ( 16 FDA reports)
BLOOD GLUCOSE DECREASED ( 16 FDA reports)
BREAST PROSTHESIS USER ( 16 FDA reports)
CARDIAC ARREST ( 16 FDA reports)
DENTURE WEARER ( 16 FDA reports)
HAEMATOMA ( 16 FDA reports)
HAEMOPTYSIS ( 16 FDA reports)
HEPATIC NEOPLASM MALIGNANT ( 16 FDA reports)
HORDEOLUM ( 16 FDA reports)
LEFT VENTRICULAR DYSFUNCTION ( 16 FDA reports)
MYELODYSPLASTIC SYNDROME ( 16 FDA reports)
NODAL OSTEOARTHRITIS ( 16 FDA reports)
PHYSICAL DISABILITY ( 16 FDA reports)
PNEUMONIA ASPIRATION ( 16 FDA reports)
PROTHROMBIN TIME PROLONGED ( 16 FDA reports)
PULMONARY MASS ( 16 FDA reports)
SUPRAVENTRICULAR TACHYCARDIA ( 16 FDA reports)
SYNOVITIS ( 16 FDA reports)
THROMBOSIS ( 16 FDA reports)
TONGUE ULCERATION ( 16 FDA reports)
UROSEPSIS ( 16 FDA reports)
WOUND COMPLICATION ( 16 FDA reports)
ACUTE RESPIRATORY DISTRESS SYNDROME ( 15 FDA reports)
AGRANULOCYTOSIS ( 15 FDA reports)
BLOOD ALBUMIN DECREASED ( 15 FDA reports)
BLOOD POTASSIUM DECREASED ( 15 FDA reports)
BLOOD UREA INCREASED ( 15 FDA reports)
BLOOD UREA NITROGEN/CREATININE RATIO INCREASED ( 15 FDA reports)
BONE GRAFT ( 15 FDA reports)
CACHEXIA ( 15 FDA reports)
CARDIOMYOPATHY ( 15 FDA reports)
COLONIC OBSTRUCTION ( 15 FDA reports)
DIVERTICULUM INTESTINAL ( 15 FDA reports)
EXCESSIVE GRANULATION TISSUE ( 15 FDA reports)
FUNGAL INFECTION ( 15 FDA reports)
HYPERBILIRUBINAEMIA ( 15 FDA reports)
LARYNGITIS ( 15 FDA reports)
MELANOCYTIC NAEVUS ( 15 FDA reports)
MOUTH ULCERATION ( 15 FDA reports)
MULTI-ORGAN FAILURE ( 15 FDA reports)
MUSCULOSKELETAL DISCOMFORT ( 15 FDA reports)
NASAL DISORDER ( 15 FDA reports)
OESTROGEN RECEPTOR ASSAY POSITIVE ( 15 FDA reports)
ORAL INFECTION ( 15 FDA reports)
PLEURECTOMY ( 15 FDA reports)
RASH PRURITIC ( 15 FDA reports)
URTICARIA ( 15 FDA reports)
VISUAL IMPAIRMENT ( 15 FDA reports)
ANIMAL BITE ( 14 FDA reports)
CARDIAC DISORDER ( 14 FDA reports)
CYSTOID MACULAR OEDEMA ( 14 FDA reports)
FACET JOINT SYNDROME ( 14 FDA reports)
HOT FLUSH ( 14 FDA reports)
HYPERGLYCAEMIA ( 14 FDA reports)
HYPERMETABOLISM ( 14 FDA reports)
LOCAL SWELLING ( 14 FDA reports)
NEUTROPENIC SEPSIS ( 14 FDA reports)
OROPHARYNGEAL PAIN ( 14 FDA reports)
PELVI-URETERIC OBSTRUCTION ( 14 FDA reports)
SKIN INFECTION ( 14 FDA reports)
THYROID NEOPLASM ( 14 FDA reports)
URINARY TRACT INFECTION ENTEROCOCCAL ( 14 FDA reports)
ABSCESS DRAINAGE ( 13 FDA reports)
ACANTHOMA ( 13 FDA reports)
ALVEOLOPLASTY ( 13 FDA reports)
ARTHROPATHY ( 13 FDA reports)
BREAST OPERATION ( 13 FDA reports)
CATHETER PLACEMENT ( 13 FDA reports)
CHOLANGITIS ( 13 FDA reports)
CONDITION AGGRAVATED ( 13 FDA reports)
CONJUNCTIVITIS ( 13 FDA reports)
DERMAL CYST ( 13 FDA reports)
DYSTHYMIC DISORDER ( 13 FDA reports)
FACE OEDEMA ( 13 FDA reports)
FAILURE TO THRIVE ( 13 FDA reports)
HAEMATURIA ( 13 FDA reports)
HYPOAESTHESIA FACIAL ( 13 FDA reports)
ILEUS ( 13 FDA reports)
JOINT SWELLING ( 13 FDA reports)
LEFT ATRIAL DILATATION ( 13 FDA reports)
NEOPLASM ( 13 FDA reports)
OSTEITIS ( 13 FDA reports)
PSEUDOMEMBRANOUS COLITIS ( 13 FDA reports)
RENAL IMPAIRMENT ( 13 FDA reports)
SKIN EXFOLIATION ( 13 FDA reports)
SOFT TISSUE INFECTION ( 13 FDA reports)
SUICIDAL IDEATION ( 13 FDA reports)
WHEEZING ( 13 FDA reports)
ACTINOMYCOSIS ( 12 FDA reports)
BODY TEMPERATURE DECREASED ( 12 FDA reports)
CALCINOSIS ( 12 FDA reports)
CARBOHYDRATE ANTIGEN 15-3 INCREASED ( 12 FDA reports)
CAROTID BODY TUMOUR ( 12 FDA reports)
CHOLELITHIASIS ( 12 FDA reports)
CORONARY ARTERY DISEASE ( 12 FDA reports)
CUSHINGOID ( 12 FDA reports)
CYST RUPTURE ( 12 FDA reports)
DELIRIUM ( 12 FDA reports)
DISSEMINATED INTRAVASCULAR COAGULATION ( 12 FDA reports)
ECCHYMOSIS ( 12 FDA reports)
EXTRAVASATION ( 12 FDA reports)
EYE IRRITATION ( 12 FDA reports)
HAEMORRHAGE ( 12 FDA reports)
HAEMORRHOIDAL HAEMORRHAGE ( 12 FDA reports)
HILAR LYMPHADENOPATHY ( 12 FDA reports)
HYPOGLYCAEMIA ( 12 FDA reports)
JAW DISORDER ( 12 FDA reports)
JOINT EFFUSION ( 12 FDA reports)
METASTASES TO NASAL SINUSES ( 12 FDA reports)
MYOCARDIAL INFARCTION ( 12 FDA reports)
NON-SMALL CELL LUNG CANCER ( 12 FDA reports)
OPTIC ATROPHY ( 12 FDA reports)
OPTIC NEUROPATHY ( 12 FDA reports)
ORAL CAVITY FISTULA ( 12 FDA reports)
PANCREATIC CALCIFICATION ( 12 FDA reports)
PELVIC FRACTURE ( 12 FDA reports)
PROTEINURIA ( 12 FDA reports)
RASH ERYTHEMATOUS ( 12 FDA reports)
SLEEP DISORDER ( 12 FDA reports)
STOMATITIS NECROTISING ( 12 FDA reports)
TOTAL LUNG CAPACITY DECREASED ( 12 FDA reports)
VENOUS INSUFFICIENCY ( 12 FDA reports)
VENOUS OCCLUSION ( 12 FDA reports)
VIITH NERVE PARALYSIS ( 12 FDA reports)
VISUAL ACUITY REDUCED ( 12 FDA reports)
WOUND INFECTION STAPHYLOCOCCAL ( 12 FDA reports)
ABDOMINAL HERNIA ( 11 FDA reports)
ABDOMINAL MASS ( 11 FDA reports)
ABDOMINAL SEPSIS ( 11 FDA reports)
AMNESIA ( 11 FDA reports)
BLOOD CULTURE POSITIVE ( 11 FDA reports)
BLOOD PRESSURE DECREASED ( 11 FDA reports)
BODY TEMPERATURE FLUCTUATION ( 11 FDA reports)
BONE LOSS ( 11 FDA reports)
BRAIN NEOPLASM MALIGNANT ( 11 FDA reports)
CARDIAC FAILURE ( 11 FDA reports)
CARDIO-RESPIRATORY ARREST ( 11 FDA reports)
CATARACT ( 11 FDA reports)
CEREBRAL HAEMORRHAGE ( 11 FDA reports)
COLD SWEAT ( 11 FDA reports)
DERMATITIS ( 11 FDA reports)
DIARRHOEA HAEMORRHAGIC ( 11 FDA reports)
DISORIENTATION ( 11 FDA reports)
DRUG HYPERSENSITIVITY ( 11 FDA reports)
DRUG TOXICITY ( 11 FDA reports)
EATING DISORDER ( 11 FDA reports)
ENDOCRINE OPHTHALMOPATHY ( 11 FDA reports)
EYELID OEDEMA ( 11 FDA reports)
HAEMATOCHEZIA ( 11 FDA reports)
ISCHAEMIA ( 11 FDA reports)
JOINT STIFFNESS ( 11 FDA reports)
LYMPHOPENIA ( 11 FDA reports)
PARKINSON'S DISEASE ( 11 FDA reports)
PERICARDIAL DRAINAGE ( 11 FDA reports)
PHARYNGITIS ( 11 FDA reports)
RHINITIS ALLERGIC ( 11 FDA reports)
SENSORY DISTURBANCE ( 11 FDA reports)
SKIN IRRITATION ( 11 FDA reports)
SPEECH DISORDER ( 11 FDA reports)
ACETABULUM FRACTURE ( 10 FDA reports)
BACTERAEMIA ( 10 FDA reports)
BALANCE DISORDER ( 10 FDA reports)
BUNDLE BRANCH BLOCK LEFT ( 10 FDA reports)
CARDIAC MURMUR ( 10 FDA reports)
CATHETER SITE HAEMATOMA ( 10 FDA reports)
CHOLECYSTITIS ( 10 FDA reports)
DEPRESSED MOOD ( 10 FDA reports)
DERMATITIS ACNEIFORM ( 10 FDA reports)
DYSPHORIA ( 10 FDA reports)
FIBROCYSTIC BREAST DISEASE ( 10 FDA reports)
FRACTURE ( 10 FDA reports)
HYPERLIPIDAEMIA ( 10 FDA reports)
HYPOACUSIS ( 10 FDA reports)
HYPOAESTHESIA ORAL ( 10 FDA reports)
HYPOVENTILATION ( 10 FDA reports)
INTERVERTEBRAL DISC SPACE NARROWING ( 10 FDA reports)
LOCALISED OEDEMA ( 10 FDA reports)
MACROPHAGES INCREASED ( 10 FDA reports)
MACULE ( 10 FDA reports)
MALNUTRITION ( 10 FDA reports)
METASTASES TO SKIN ( 10 FDA reports)
MOUTH HAEMORRHAGE ( 10 FDA reports)
OBSTRUCTIVE AIRWAYS DISORDER ( 10 FDA reports)
OSTEITIS DEFORMANS ( 10 FDA reports)
OVARIAN MASS ( 10 FDA reports)
PALATAL DISORDER ( 10 FDA reports)
PRODUCTIVE COUGH ( 10 FDA reports)
PULMONARY CONGESTION ( 10 FDA reports)
RECTAL HAEMORRHAGE ( 10 FDA reports)
RESPIRATORY RATE INCREASED ( 10 FDA reports)
SALPINGO-OOPHORECTOMY BILATERAL ( 10 FDA reports)
SCAR ( 10 FDA reports)
STREPTOCOCCAL INFECTION ( 10 FDA reports)
TUMOUR MARKER INCREASED ( 10 FDA reports)
ABDOMINAL PAIN UPPER ( 9 FDA reports)
ACANTHOLYSIS ( 9 FDA reports)
ACTIVITIES OF DAILY LIVING IMPAIRED ( 9 FDA reports)
ARTERIOSCLEROSIS ( 9 FDA reports)
BACTERIAL TEST POSITIVE ( 9 FDA reports)
BAND NEUTROPHIL COUNT INCREASED ( 9 FDA reports)
BLISTER ( 9 FDA reports)
BLOOD CALCIUM DECREASED ( 9 FDA reports)
BODY HEIGHT DECREASED ( 9 FDA reports)
BONE MARROW OEDEMA ( 9 FDA reports)
BRAIN OPERATION ( 9 FDA reports)
BURNING SENSATION ( 9 FDA reports)
CARDIOPULMONARY FAILURE ( 9 FDA reports)
CHEILITIS ( 9 FDA reports)
CSF TEST ABNORMAL ( 9 FDA reports)
CYST DRAINAGE ( 9 FDA reports)
DENTAL OPERATION ( 9 FDA reports)
DRUG INEFFECTIVE ( 9 FDA reports)
EYE PAIN ( 9 FDA reports)
FIBROMYALGIA ( 9 FDA reports)
FLUSHING ( 9 FDA reports)
GASTROENTERITIS VIRAL ( 9 FDA reports)
GENERALISED OEDEMA ( 9 FDA reports)
GOITRE ( 9 FDA reports)
INTERNATIONAL NORMALISED RATIO INCREASED ( 9 FDA reports)
INTESTINAL OBSTRUCTION ( 9 FDA reports)
JAUNDICE ( 9 FDA reports)
LESION EXCISION ( 9 FDA reports)
MACROCYTOSIS ( 9 FDA reports)
METASTASES TO CHEST WALL ( 9 FDA reports)
METASTASES TO MENINGES ( 9 FDA reports)
NEUROPATHY ( 9 FDA reports)
OSTEOLYSIS ( 9 FDA reports)
OVARIAN CYST ( 9 FDA reports)
PERINEURIAL CYST ( 9 FDA reports)
PLEURODESIS ( 9 FDA reports)
RADIOTHERAPY ( 9 FDA reports)
ROTATOR CUFF SYNDROME ( 9 FDA reports)
SENSORY LOSS ( 9 FDA reports)
SYNOVIAL CYST ( 9 FDA reports)
THORACOSTOMY ( 9 FDA reports)
THYROID CYST ( 9 FDA reports)
TOOTH FRACTURE ( 9 FDA reports)
TOOTH REPAIR ( 9 FDA reports)
TRANSFUSION ( 9 FDA reports)
WEIGHT INCREASED ( 9 FDA reports)
AGEUSIA ( 8 FDA reports)
ALTERED STATE OF CONSCIOUSNESS ( 8 FDA reports)
ANGIOEDEMA ( 8 FDA reports)
AORTIC VALVE DISEASE ( 8 FDA reports)
APICECTOMY ( 8 FDA reports)
ARTHROFIBROSIS ( 8 FDA reports)
ARTIFICIAL CROWN PROCEDURE ( 8 FDA reports)
ASPIRATION ( 8 FDA reports)
ATAXIA ( 8 FDA reports)
BLINDNESS TRANSIENT ( 8 FDA reports)
CERVICAL SPINAL STENOSIS ( 8 FDA reports)
CERVIX CARCINOMA ( 8 FDA reports)
CHROMATOPSIA ( 8 FDA reports)
COLONIC POLYP ( 8 FDA reports)
CRYOTHERAPY ( 8 FDA reports)
DIABETIC FOOT ( 8 FDA reports)
DIALYSIS ( 8 FDA reports)
DIVERTICULUM ( 8 FDA reports)
DYSARTHRIA ( 8 FDA reports)
DYSFUNCTIONAL UTERINE BLEEDING ( 8 FDA reports)
ELECTROENCEPHALOGRAM ABNORMAL ( 8 FDA reports)
ENCEPHALOMALACIA ( 8 FDA reports)
FACIAL BONES FRACTURE ( 8 FDA reports)
FACIAL PAIN ( 8 FDA reports)
FEMORAL NECK FRACTURE ( 8 FDA reports)
FLUID OVERLOAD ( 8 FDA reports)
FOOT DEFORMITY ( 8 FDA reports)
GASTROINTESTINAL DISORDER ( 8 FDA reports)
GINGIVAL EROSION ( 8 FDA reports)
HEAD INJURY ( 8 FDA reports)
HEPATIC LESION ( 8 FDA reports)
HEPATITIS C ( 8 FDA reports)
HYDROPNEUMOTHORAX ( 8 FDA reports)
HYPERCHOLESTEROLAEMIA ( 8 FDA reports)
HYPOPHOSPHATAEMIA ( 8 FDA reports)
INCISIONAL DRAINAGE ( 8 FDA reports)
LACERATION ( 8 FDA reports)
LEFT VENTRICULAR HYPERTROPHY ( 8 FDA reports)
MEDICAL DEVICE COMPLICATION ( 8 FDA reports)
MENISCUS LESION ( 8 FDA reports)
METASTASES TO PELVIS ( 8 FDA reports)
MOVEMENT DISORDER ( 8 FDA reports)
NERVE BLOCK ( 8 FDA reports)
NORMOCHROMIC NORMOCYTIC ANAEMIA ( 8 FDA reports)
ORAL DISCOMFORT ( 8 FDA reports)
OSTEOSYNTHESIS ( 8 FDA reports)
OXYGEN SATURATION DECREASED ( 8 FDA reports)
PANCREATIC CYST ( 8 FDA reports)
PERIPHERAL VASCULAR DISORDER ( 8 FDA reports)
PERONEAL NERVE PALSY ( 8 FDA reports)
PETECHIAE ( 8 FDA reports)
PHLEBOLITH ( 8 FDA reports)
PNEUMATOSIS INTESTINALIS ( 8 FDA reports)
POOR PERSONAL HYGIENE ( 8 FDA reports)
POSITIVE ROMBERGISM ( 8 FDA reports)
PULMONARY HILUM MASS ( 8 FDA reports)
RADICULITIS ( 8 FDA reports)
RADIUS FRACTURE ( 8 FDA reports)
RED BLOOD CELL COUNT DECREASED ( 8 FDA reports)
RESPIRATORY DISTRESS ( 8 FDA reports)
SEASONAL ALLERGY ( 8 FDA reports)
SINGLE FUNCTIONAL KIDNEY ( 8 FDA reports)
SINUS BRADYCARDIA ( 8 FDA reports)
SLEEP APNOEA SYNDROME ( 8 FDA reports)
SOFT TISSUE DISORDER ( 8 FDA reports)
STAPHYLOCOCCAL INFECTION ( 8 FDA reports)
TACHYARRHYTHMIA ( 8 FDA reports)
UMBILICAL HERNIA ( 8 FDA reports)
VARICOSE VEIN ( 8 FDA reports)
VEIN DISORDER ( 8 FDA reports)
ABDOMINAL DISCOMFORT ( 7 FDA reports)
ANOREXIA ( 7 FDA reports)
ANOSMIA ( 7 FDA reports)
BLOOD CHOLESTEROL INCREASED ( 7 FDA reports)
BLOOD PRESSURE INCREASED ( 7 FDA reports)
BONE FORMATION INCREASED ( 7 FDA reports)
BRAIN SCAN ABNORMAL ( 7 FDA reports)
BREAST ATROPHY ( 7 FDA reports)
BREAST RECONSTRUCTION ( 7 FDA reports)
CARDIAC TAMPONADE ( 7 FDA reports)
CEREBRAL DISORDER ( 7 FDA reports)
CYSTITIS ( 7 FDA reports)
DYSSTASIA ( 7 FDA reports)
EATING DISORDER SYMPTOM ( 7 FDA reports)
ENDOMETRIAL DISORDER ( 7 FDA reports)
ENTERITIS INFECTIOUS ( 7 FDA reports)
EXOSTOSIS ( 7 FDA reports)
EYE HAEMORRHAGE ( 7 FDA reports)
GASTROENTERITIS ( 7 FDA reports)
GASTROINTESTINAL SOUNDS ABNORMAL ( 7 FDA reports)
GASTROSTOMY TUBE INSERTION ( 7 FDA reports)
GINGIVAL DISORDER ( 7 FDA reports)
HAEMANGIOMA OF LIVER ( 7 FDA reports)
HAEMODIALYSIS ( 7 FDA reports)
HEPATIC ENZYME INCREASED ( 7 FDA reports)
HEPATOTOXICITY ( 7 FDA reports)
HIGH FREQUENCY ABLATION ( 7 FDA reports)
HIP FRACTURE ( 7 FDA reports)
IMPETIGO ( 7 FDA reports)
INTERVERTEBRAL DISC DISORDER ( 7 FDA reports)
IRRITABLE BOWEL SYNDROME ( 7 FDA reports)
JAUNDICE CHOLESTATIC ( 7 FDA reports)
JAW OPERATION ( 7 FDA reports)
LYMPHATIC DISORDER ( 7 FDA reports)
MASTECTOMY ( 7 FDA reports)
MICTURITION URGENCY ( 7 FDA reports)
NAIL AVULSION ( 7 FDA reports)
OBSTRUCTION ( 7 FDA reports)
ODYNOPHAGIA ( 7 FDA reports)
PAINFUL DEFAECATION ( 7 FDA reports)
PULMONARY OEDEMA ( 7 FDA reports)
RASH MACULO-PAPULAR ( 7 FDA reports)
RECTAL FISSURE ( 7 FDA reports)
SALIVARY GLAND DISORDER ( 7 FDA reports)
SENSATION OF PRESSURE ( 7 FDA reports)
SHOCK ( 7 FDA reports)
SKELETAL INJURY ( 7 FDA reports)
SKIN ATROPHY ( 7 FDA reports)
SPINAL CORD COMPRESSION ( 7 FDA reports)
STUPOR ( 7 FDA reports)
SUBDURAL HAEMATOMA ( 7 FDA reports)
TUBULOINTERSTITIAL NEPHRITIS ( 7 FDA reports)
WOUND DRAINAGE ( 7 FDA reports)
ACQUIRED DIAPHRAGMATIC EVENTRATION ( 6 FDA reports)
ACQUIRED OESOPHAGEAL WEB ( 6 FDA reports)
ACUTE RESPIRATORY FAILURE ( 6 FDA reports)
ALPHA HAEMOLYTIC STREPTOCOCCAL INFECTION ( 6 FDA reports)
AORTIC CALCIFICATION ( 6 FDA reports)
AORTIC VALVE SCLEROSIS ( 6 FDA reports)
APHONIA ( 6 FDA reports)
APPENDICECTOMY ( 6 FDA reports)
BENIGN NEOPLASM OF THYROID GLAND ( 6 FDA reports)
BILIARY DILATATION ( 6 FDA reports)
BLOOD LACTATE DEHYDROGENASE INCREASED ( 6 FDA reports)
BONE EROSION ( 6 FDA reports)
BREAST LUMP REMOVAL ( 6 FDA reports)
CAROTID ARTERY DISEASE ( 6 FDA reports)
CENTRAL NERVOUS SYSTEM LESION ( 6 FDA reports)
CERVICITIS ( 6 FDA reports)
CHOLECYSTECTOMY ( 6 FDA reports)
COCCYDYNIA ( 6 FDA reports)
COLON NEOPLASM ( 6 FDA reports)
CULTURE URINE POSITIVE ( 6 FDA reports)
CYST ASPIRATION ( 6 FDA reports)
DEFAECATION URGENCY ( 6 FDA reports)
EDENTULOUS ( 6 FDA reports)
EPILEPSY ( 6 FDA reports)
EYE NAEVUS ( 6 FDA reports)
FAECALOMA ( 6 FDA reports)
GASTRIC ULCER ( 6 FDA reports)
GASTROINTESTINAL OBSTRUCTION ( 6 FDA reports)
GINGIVAL ERYTHEMA ( 6 FDA reports)
GLAUCOMA ( 6 FDA reports)
GRANULOMA ( 6 FDA reports)
HAEMORRHAGE INTRACRANIAL ( 6 FDA reports)
HEPATITIS ( 6 FDA reports)
HEPATITIS FULMINANT ( 6 FDA reports)
HERNIA REPAIR ( 6 FDA reports)
HYPERCALCAEMIA ( 6 FDA reports)
HYPERKERATOSIS ( 6 FDA reports)
HYPERURICAEMIA ( 6 FDA reports)
HYPOMAGNESAEMIA ( 6 FDA reports)
HYSTERECTOMY ( 6 FDA reports)
INFLAMMATORY CARCINOMA OF THE BREAST ( 6 FDA reports)
INTRACRANIAL TUMOUR HAEMORRHAGE ( 6 FDA reports)
LOCALISED INFECTION ( 6 FDA reports)
LUMBAR VERTEBRAL FRACTURE ( 6 FDA reports)
LYMPHOMA ( 6 FDA reports)
MAGNESIUM DEFICIENCY ( 6 FDA reports)
MALIGNANT ASCITES ( 6 FDA reports)
MAXILLOFACIAL OPERATION ( 6 FDA reports)
METASTASES TO ABDOMINAL CAVITY ( 6 FDA reports)
METASTASES TO THE MEDIASTINUM ( 6 FDA reports)
MYOPATHY ( 6 FDA reports)
NASAL DISCOMFORT ( 6 FDA reports)
OEDEMA MUCOSAL ( 6 FDA reports)
OPTIC NERVE DISORDER ( 6 FDA reports)
ORAL HERPES ( 6 FDA reports)
PANCREATIC NEOPLASM ( 6 FDA reports)
PARANASAL SINUS MUCOSAL HYPERTROPHY ( 6 FDA reports)
PERIARTHRITIS ( 6 FDA reports)
PERIODONTAL INFECTION ( 6 FDA reports)
PERIODONTAL OPERATION ( 6 FDA reports)
PLANTAR FASCIITIS ( 6 FDA reports)
PROCTALGIA ( 6 FDA reports)
PULMONARY VALVE INCOMPETENCE ( 6 FDA reports)
RADICULAR SYNDROME ( 6 FDA reports)
RASH MACULAR ( 6 FDA reports)
REFLUX LARYNGITIS ( 6 FDA reports)
RENAL ATROPHY ( 6 FDA reports)
RESTLESSNESS ( 6 FDA reports)
SINUS OPERATION ( 6 FDA reports)
SKIN DISORDER ( 6 FDA reports)
TOOTH IMPACTED ( 6 FDA reports)
TRACHEOSTOMY ( 6 FDA reports)
TRAUMATIC HAEMATOMA ( 6 FDA reports)
UMBILICAL HERNIA REPAIR ( 6 FDA reports)
UTERINE CERVICAL SQUAMOUS METAPLASIA ( 6 FDA reports)
VASOGENIC CEREBRAL OEDEMA ( 6 FDA reports)
VERTEBRAL FORAMINAL STENOSIS ( 6 FDA reports)
ABSCESS INTESTINAL ( 5 FDA reports)
ACTINIC KERATOSIS ( 5 FDA reports)
ADENOCARCINOMA ( 5 FDA reports)
ADJUSTMENT DISORDER ( 5 FDA reports)
AFFECTIVE DISORDER ( 5 FDA reports)
ANAPHYLACTIC REACTION ( 5 FDA reports)
ANAPHYLACTIC SHOCK ( 5 FDA reports)
ANASTOMOTIC LEAK ( 5 FDA reports)
ATROPHIC VULVOVAGINITIS ( 5 FDA reports)
BLOOD PRESSURE DIASTOLIC DECREASED ( 5 FDA reports)
BLOOD PRESSURE SYSTOLIC INCREASED ( 5 FDA reports)
BLOOD TRIGLYCERIDES INCREASED ( 5 FDA reports)
BONE DENSITY DECREASED ( 5 FDA reports)
BREATH SOUNDS ABNORMAL ( 5 FDA reports)
BRONCHIAL NEOPLASM ( 5 FDA reports)
BRONCHIECTASIS ( 5 FDA reports)
CALCULUS URETERIC ( 5 FDA reports)
CERVICOBRACHIAL SYNDROME ( 5 FDA reports)
CHOKING ( 5 FDA reports)
COORDINATION ABNORMAL ( 5 FDA reports)
CORNEAL OEDEMA ( 5 FDA reports)
DEMENTIA ALZHEIMER'S TYPE ( 5 FDA reports)
DENTAL PLAQUE ( 5 FDA reports)
DIVERTICULITIS ( 5 FDA reports)
DRUG DEPENDENCE ( 5 FDA reports)
DRUG DOSE OMISSION ( 5 FDA reports)
DRUG WITHDRAWAL SYNDROME ( 5 FDA reports)
ELECTROCARDIOGRAM QT PROLONGED ( 5 FDA reports)
ELECTROCARDIOGRAM T WAVE INVERSION ( 5 FDA reports)
ESCHERICHIA INFECTION ( 5 FDA reports)
FACE INJURY ( 5 FDA reports)
FAECAL INCONTINENCE ( 5 FDA reports)
FIBROSIS ( 5 FDA reports)
GALLBLADDER ENLARGEMENT ( 5 FDA reports)
GASTROINTESTINAL PERFORATION ( 5 FDA reports)
HAEMATEMESIS ( 5 FDA reports)
IMMUNE SYSTEM DISORDER ( 5 FDA reports)
IMPULSIVE BEHAVIOUR ( 5 FDA reports)
INFLUENZA LIKE ILLNESS ( 5 FDA reports)
IRON DEFICIENCY ANAEMIA ( 5 FDA reports)
JAW LESION EXCISION ( 5 FDA reports)
JOINT SPRAIN ( 5 FDA reports)
JUGULAR VEIN THROMBOSIS ( 5 FDA reports)
LYMPHOCYTE COUNT DECREASED ( 5 FDA reports)
MALIGNANT NEOPLASM OF SPINAL CORD ( 5 FDA reports)
MENORRHAGIA ( 5 FDA reports)
MUCOSAL ULCERATION ( 5 FDA reports)
MUSCULOSKELETAL CHEST PAIN ( 5 FDA reports)
ONYCHOMADESIS ( 5 FDA reports)
ORAL INTAKE REDUCED ( 5 FDA reports)
ORAL SUBMUCOSAL FIBROSIS ( 5 FDA reports)
ORBITAL OEDEMA ( 5 FDA reports)
PANCREATIC ATROPHY ( 5 FDA reports)
PANCREATITIS ( 5 FDA reports)
PANIC DISORDER ( 5 FDA reports)
PARANOIA ( 5 FDA reports)
PELVIC PAIN ( 5 FDA reports)
PEPTIC ULCER ( 5 FDA reports)
PERICARDIAL EXCISION ( 5 FDA reports)
PERICARDITIS ( 5 FDA reports)
PERIODONTAL DISEASE ( 5 FDA reports)
PLATELET DISORDER ( 5 FDA reports)
PORTAL VEIN THROMBOSIS ( 5 FDA reports)
PSEUDOMONAL BACTERAEMIA ( 5 FDA reports)
PYELONEPHRITIS ( 5 FDA reports)
REACTIVE PSYCHOSIS ( 5 FDA reports)
RESPIRATORY DEPRESSION ( 5 FDA reports)
SKIN TOXICITY ( 5 FDA reports)
STAPHYLOCOCCAL BACTERAEMIA ( 5 FDA reports)
STENT PLACEMENT ( 5 FDA reports)
SUDDEN DEATH ( 5 FDA reports)
THYROID DISORDER ( 5 FDA reports)
UNEVALUABLE EVENT ( 5 FDA reports)
URETERIC OBSTRUCTION ( 5 FDA reports)
UTERINE POLYP ( 5 FDA reports)
WHITE BLOOD CELLS URINE POSITIVE ( 5 FDA reports)
WOUND INFECTION ( 5 FDA reports)
ACUTE MYOCARDIAL INFARCTION ( 4 FDA reports)
APHASIA ( 4 FDA reports)
APHTHOUS STOMATITIS ( 4 FDA reports)
ARRHYTHMIA SUPRAVENTRICULAR ( 4 FDA reports)
BLADDER PAIN ( 4 FDA reports)
BLOOD CHLORIDE DECREASED ( 4 FDA reports)
BLOOD PH DECREASED ( 4 FDA reports)
BLOOD PHOSPHORUS DECREASED ( 4 FDA reports)
BLOOD UREA DECREASED ( 4 FDA reports)
BONE MARROW FAILURE ( 4 FDA reports)
BRADYKINESIA ( 4 FDA reports)
BREAST ABSCESS ( 4 FDA reports)
BREAST CANCER FEMALE ( 4 FDA reports)
CARDIAC FLUTTER ( 4 FDA reports)
CAROTID BRUIT ( 4 FDA reports)
CENTRAL LINE INFECTION ( 4 FDA reports)
CHEST TUBE INSERTION ( 4 FDA reports)
CHONDROMALACIA ( 4 FDA reports)
CLOSTRIDIAL INFECTION ( 4 FDA reports)
COMA HEPATIC ( 4 FDA reports)
CONTUSION ( 4 FDA reports)
DENTAL CARE ( 4 FDA reports)
DIFFUSE ALVEOLAR DAMAGE ( 4 FDA reports)
DIVERTICULAR PERFORATION ( 4 FDA reports)
DRUG INTERACTION ( 4 FDA reports)
DUODENAL ULCER ( 4 FDA reports)
ENTEROCOLITIS INFECTIOUS ( 4 FDA reports)
FEELING ABNORMAL ( 4 FDA reports)
FOOD POISONING ( 4 FDA reports)
GASTRIC PERFORATION ( 4 FDA reports)
GRANULOCYTE COUNT DECREASED ( 4 FDA reports)
HEPATOSPLENOMEGALY ( 4 FDA reports)
HIGH DENSITY LIPOPROTEIN DECREASED ( 4 FDA reports)
HIP ARTHROPLASTY ( 4 FDA reports)
HYDROCEPHALUS ( 4 FDA reports)
HYPERCOAGULATION ( 4 FDA reports)
IDIOPATHIC THROMBOCYTOPENIC PURPURA ( 4 FDA reports)
IMMUNOSUPPRESSION ( 4 FDA reports)
IMPAIRED SELF-CARE ( 4 FDA reports)
INAPPROPRIATE ANTIDIURETIC HORMONE SECRETION ( 4 FDA reports)
INFUSION RELATED REACTION ( 4 FDA reports)
KERATITIS ( 4 FDA reports)
LEUKOCYTOCLASTIC VASCULITIS ( 4 FDA reports)
LICHEN PLANUS ( 4 FDA reports)
LOBAR PNEUMONIA ( 4 FDA reports)
MECHANICAL VENTILATION ( 4 FDA reports)
MENINGIOMA ( 4 FDA reports)
METASTASES TO SPLEEN ( 4 FDA reports)
METASTASIS ( 4 FDA reports)
MITRAL VALVE CALCIFICATION ( 4 FDA reports)
MUSCLE TWITCHING ( 4 FDA reports)
MYDRIASIS ( 4 FDA reports)
NASAL CONGESTION ( 4 FDA reports)
NERVOUSNESS ( 4 FDA reports)
NEUTROPENIC INFECTION ( 4 FDA reports)
NO THERAPEUTIC RESPONSE ( 4 FDA reports)
ORTHOSTATIC HYPOTENSION ( 4 FDA reports)
PARKINSONIAN GAIT ( 4 FDA reports)
PERINEAL ABSCESS ( 4 FDA reports)
PLEURITIC PAIN ( 4 FDA reports)
POLYMYOSITIS ( 4 FDA reports)
PORTAL HYPERTENSION ( 4 FDA reports)
PRESYNCOPE ( 4 FDA reports)
PROTEIN TOTAL DECREASED ( 4 FDA reports)
PULMONARY HYPERTENSION ( 4 FDA reports)
RADIATION INJURY ( 4 FDA reports)
RALES ( 4 FDA reports)
REFUSAL OF TREATMENT BY PATIENT ( 4 FDA reports)
RENAL DISORDER ( 4 FDA reports)
RENAL FAILURE CHRONIC ( 4 FDA reports)
RESPIRATORY DISORDER ( 4 FDA reports)
RHINITIS ( 4 FDA reports)
SENSITIVITY OF TEETH ( 4 FDA reports)
SEPSIS SYNDROME ( 4 FDA reports)
SEROSITIS ( 4 FDA reports)
SKIN LESION EXCISION ( 4 FDA reports)
SKIN REACTION ( 4 FDA reports)
STEVENS-JOHNSON SYNDROME ( 4 FDA reports)
TACHYPNOEA ( 4 FDA reports)
THORACOTOMY ( 4 FDA reports)
TONGUE DISORDER ( 4 FDA reports)
TRANSAMINASES INCREASED ( 4 FDA reports)
TUMOUR NECROSIS ( 4 FDA reports)
UPPER GASTROINTESTINAL HAEMORRHAGE ( 4 FDA reports)
URINARY BLADDER HAEMORRHAGE ( 4 FDA reports)
URINE OUTPUT DECREASED ( 4 FDA reports)
VENTRICULAR HYPERTROPHY ( 4 FDA reports)
VERY LOW DENSITY LIPOPROTEIN INCREASED ( 4 FDA reports)
WOUND DEBRIDEMENT ( 4 FDA reports)
WOUND SECRETION ( 4 FDA reports)
ABSCESS NECK ( 3 FDA reports)
ACUTE SINUSITIS ( 3 FDA reports)
ADENOMATOUS POLYPOSIS COLI ( 3 FDA reports)
ADHESION ( 3 FDA reports)
ANTIBIOTIC RESISTANT STAPHYLOCOCCUS TEST POSITIVE ( 3 FDA reports)
ARRHYTHMIA ( 3 FDA reports)
ARTHRITIS BACTERIAL ( 3 FDA reports)
AVULSION FRACTURE ( 3 FDA reports)
BACTERIA URINE IDENTIFIED ( 3 FDA reports)
BLADDER HYPERTROPHY ( 3 FDA reports)
BLEPHARITIS ( 3 FDA reports)
BLOOD CREATININE ( 3 FDA reports)
BONE LESION EXCISION ( 3 FDA reports)
BRAIN MASS ( 3 FDA reports)
BUNDLE BRANCH BLOCK RIGHT ( 3 FDA reports)
CARDIAC VALVE DISEASE ( 3 FDA reports)
CENTRAL NERVOUS SYSTEM INFLAMMATION ( 3 FDA reports)
CEREBRAL ISCHAEMIA ( 3 FDA reports)
CHOLESTASIS ( 3 FDA reports)
CLAVICLE FRACTURE ( 3 FDA reports)
COELIAC DISEASE ( 3 FDA reports)
COLITIS ISCHAEMIC ( 3 FDA reports)
CRANIAL NEUROPATHY ( 3 FDA reports)
DACRYOSTENOSIS ACQUIRED ( 3 FDA reports)
DERMATITIS BULLOUS ( 3 FDA reports)
DIABETIC ENTEROPATHY ( 3 FDA reports)
DIABETIC ULCER ( 3 FDA reports)
DUODENAL OBSTRUCTION ( 3 FDA reports)
DYSCHEZIA ( 3 FDA reports)
DYSPNOEA AT REST ( 3 FDA reports)
ECZEMA ( 3 FDA reports)
ELECTROCARDIOGRAM QRS COMPLEX ABNORMAL ( 3 FDA reports)
ELECTROCARDIOGRAM T WAVE ABNORMAL ( 3 FDA reports)
EMBOLISM ( 3 FDA reports)
EUSTACHIAN TUBE DYSFUNCTION ( 3 FDA reports)
EYE INFECTION ( 3 FDA reports)
FEELING COLD ( 3 FDA reports)
FLATULENCE ( 3 FDA reports)
GLOSSODYNIA ( 3 FDA reports)
GRAND MAL CONVULSION ( 3 FDA reports)
HEMIPARESIS ( 3 FDA reports)
HEPATIC NECROSIS ( 3 FDA reports)
HYPOALBUMINAEMIA ( 3 FDA reports)
HYPOGAMMAGLOBULINAEMIA ( 3 FDA reports)
HYPOPNOEA ( 3 FDA reports)
HYPOVOLAEMIA ( 3 FDA reports)
INCONTINENCE ( 3 FDA reports)
INTESTINAL FUNCTIONAL DISORDER ( 3 FDA reports)
INTESTINAL PERFORATION ( 3 FDA reports)
INTRAVASCULAR HAEMOLYSIS ( 3 FDA reports)
KLEBSIELLA BACTERAEMIA ( 3 FDA reports)
KLEBSIELLA INFECTION ( 3 FDA reports)
LACTIC ACIDOSIS ( 3 FDA reports)
LACUNAR INFARCTION ( 3 FDA reports)
LUNG CONSOLIDATION ( 3 FDA reports)
LUNG INFECTION ( 3 FDA reports)
MACULAR HOLE ( 3 FDA reports)
MADAROSIS ( 3 FDA reports)
MELAENA ( 3 FDA reports)
MENOPAUSAL SYMPTOMS ( 3 FDA reports)
METABOLIC DISORDER ( 3 FDA reports)
METASTASES TO PERITONEUM ( 3 FDA reports)
MICTURITION DISORDER ( 3 FDA reports)
MIGRAINE ( 3 FDA reports)
MUSCLE ATROPHY ( 3 FDA reports)
MUSCULOSKELETAL DISORDER ( 3 FDA reports)
MYELITIS TRANSVERSE ( 3 FDA reports)
MYELOPATHY ( 3 FDA reports)
NERVOUS SYSTEM DISORDER ( 3 FDA reports)
NEURODERMATITIS ( 3 FDA reports)
NEUROTOXICITY ( 3 FDA reports)
NIGHT BLINDNESS ( 3 FDA reports)
OCULAR HYPERAEMIA ( 3 FDA reports)
OCULAR ICTERUS ( 3 FDA reports)
OESOPHAGEAL PERFORATION ( 3 FDA reports)
ORAL FIBROMA ( 3 FDA reports)
ORAL SURGERY ( 3 FDA reports)
OROANTRAL FISTULA ( 3 FDA reports)
OTITIS EXTERNA ( 3 FDA reports)
OXYGEN SUPPLEMENTATION ( 3 FDA reports)
PARACENTESIS ( 3 FDA reports)
PARAPLEGIA ( 3 FDA reports)
PERIPHERAL COLDNESS ( 3 FDA reports)
PERIPHERAL MOTOR NEUROPATHY ( 3 FDA reports)
PHARYNGEAL INFLAMMATION ( 3 FDA reports)
PHARYNGOLARYNGEAL PAIN ( 3 FDA reports)
PLASMACYTOSIS ( 3 FDA reports)
PLATELET ADHESIVENESS INCREASED ( 3 FDA reports)
PNEUMOCYSTIS JIROVECI PNEUMONIA ( 3 FDA reports)
PNEUMONITIS CHEMICAL ( 3 FDA reports)
POLLAKIURIA ( 3 FDA reports)
POST PROCEDURAL COMPLICATION ( 3 FDA reports)
POSTICTAL STATE ( 3 FDA reports)
PRESBYACUSIS ( 3 FDA reports)
PULPITIS DENTAL ( 3 FDA reports)
RASH GENERALISED ( 3 FDA reports)
RECTAL ULCER ( 3 FDA reports)
REGURGITATION ( 3 FDA reports)
RESPIRATORY ARREST ( 3 FDA reports)
RETCHING ( 3 FDA reports)
RETINAL HAEMORRHAGE ( 3 FDA reports)
RHABDOMYOLYSIS ( 3 FDA reports)
RHINALGIA ( 3 FDA reports)
ROAD TRAFFIC ACCIDENT ( 3 FDA reports)
SCOTOMA ( 3 FDA reports)
SKIN CHAPPED ( 3 FDA reports)
SKIN DISCOLOURATION ( 3 FDA reports)
SKIN ULCER ( 3 FDA reports)
SPINAL CORD INJURY THORACIC ( 3 FDA reports)
SPLENIC CYST ( 3 FDA reports)
STAG HORN CALCULUS ( 3 FDA reports)
TEMPORAL ARTERITIS ( 3 FDA reports)
THYROGLOBULIN INCREASED ( 3 FDA reports)
THYROID CANCER ( 3 FDA reports)
THYROID MASS ( 3 FDA reports)
TOXIC EPIDERMAL NECROLYSIS ( 3 FDA reports)
TOXIC OPTIC NEUROPATHY ( 3 FDA reports)
TUMOUR LYSIS SYNDROME ( 3 FDA reports)
URINARY INCONTINENCE ( 3 FDA reports)
VITAMIN A DEFICIENCY ( 3 FDA reports)
ABASIA ( 2 FDA reports)
ABDOMINAL PAIN LOWER ( 2 FDA reports)
ABSCESS LIMB ( 2 FDA reports)
ABSCESS RUPTURE ( 2 FDA reports)
ACTIVATED PARTIAL THROMBOPLASTIN TIME SHORTENED ( 2 FDA reports)
ACUTE LYMPHOCYTIC LEUKAEMIA ( 2 FDA reports)
ACUTE PULMONARY OEDEMA ( 2 FDA reports)
ADVERSE EVENT ( 2 FDA reports)
AFFECT LABILITY ( 2 FDA reports)
AMENORRHOEA ( 2 FDA reports)
ANAEMIA OF MALIGNANT DISEASE ( 2 FDA reports)
ANASTOMOTIC ULCER ( 2 FDA reports)
APNOEA ( 2 FDA reports)
ARTERIAL THROMBOSIS ( 2 FDA reports)
ASPERGILLOSIS ( 2 FDA reports)
AUTONOMIC NERVOUS SYSTEM IMBALANCE ( 2 FDA reports)
BACTERIA STOOL IDENTIFIED ( 2 FDA reports)
BILIARY COLIC ( 2 FDA reports)
BLINDNESS ( 2 FDA reports)
BLOOD CREATININE DECREASED ( 2 FDA reports)
BLOOD POTASSIUM INCREASED ( 2 FDA reports)
BLOOD PRESSURE SYSTOLIC DECREASED ( 2 FDA reports)
BLOOD TEST NORMAL ( 2 FDA reports)
BLOOD THYROID STIMULATING HORMONE INCREASED ( 2 FDA reports)
BONE CYST ( 2 FDA reports)
BONE NEOPLASM MALIGNANT ( 2 FDA reports)
BRAIN OEDEMA ( 2 FDA reports)
BREAST CELLULITIS ( 2 FDA reports)
C-REACTIVE PROTEIN DECREASED ( 2 FDA reports)
CARBON DIOXIDE DECREASED ( 2 FDA reports)
CARDIOTOXICITY ( 2 FDA reports)
CEREBROVASCULAR ACCIDENT ( 2 FDA reports)
CHOLANGITIS ACUTE ( 2 FDA reports)
CIRCULATORY COLLAPSE ( 2 FDA reports)
COGNITIVE DISORDER ( 2 FDA reports)
COLON CANCER METASTATIC ( 2 FDA reports)
COLONIC STENOSIS ( 2 FDA reports)
CULTURE POSITIVE ( 2 FDA reports)
CYTOMEGALOVIRUS INFECTION ( 2 FDA reports)
DEMYELINATION ( 2 FDA reports)
DENTAL FISTULA ( 2 FDA reports)
DENTAL NECROSIS ( 2 FDA reports)
DILATATION VENTRICULAR ( 2 FDA reports)
DISEASE RECURRENCE ( 2 FDA reports)
DYSPLASIA ( 2 FDA reports)
EFFUSION ( 2 FDA reports)
ELECTROLYTE IMBALANCE ( 2 FDA reports)
EMBOLISM VENOUS ( 2 FDA reports)
ENTEROCOLITIS ( 2 FDA reports)
ENTEROCUTANEOUS FISTULA ( 2 FDA reports)
ERUCTATION ( 2 FDA reports)
ESCHERICHIA BACTERAEMIA ( 2 FDA reports)
ESCHERICHIA SEPSIS ( 2 FDA reports)
EYE DISORDER ( 2 FDA reports)
EYELID PTOSIS ( 2 FDA reports)
FACIAL WASTING ( 2 FDA reports)
FAECES DISCOLOURED ( 2 FDA reports)
FEAR ( 2 FDA reports)
FEEDING TUBE COMPLICATION ( 2 FDA reports)
FEMORAL HERNIA, OBSTRUCTIVE ( 2 FDA reports)
FIBRIN D DIMER INCREASED ( 2 FDA reports)
FLUID INTAKE REDUCED ( 2 FDA reports)
GASTROINTESTINAL FISTULA ( 2 FDA reports)
GASTROINTESTINAL INFECTION ( 2 FDA reports)
GENERALISED ERYTHEMA ( 2 FDA reports)
GINGIVAL ABSCESS ( 2 FDA reports)
GINGIVAL INFECTION ( 2 FDA reports)
GINGIVAL RECESSION ( 2 FDA reports)
GLIOSIS ( 2 FDA reports)
GLOMERULAR FILTRATION RATE DECREASED ( 2 FDA reports)
GROIN ABSCESS ( 2 FDA reports)
HAEMANGIOMA ( 2 FDA reports)
HAEMOLYTIC ANAEMIA ( 2 FDA reports)
HAEMORRHAGE SUBCUTANEOUS ( 2 FDA reports)
HAEMORRHAGIC ANAEMIA ( 2 FDA reports)
HEAD AND NECK CANCER ( 2 FDA reports)
HEARING IMPAIRED ( 2 FDA reports)
HEART VALVE INCOMPETENCE ( 2 FDA reports)
HEPATIC HAEMATOMA ( 2 FDA reports)
HEPATIC NEOPLASM ( 2 FDA reports)
HEPATIC VEIN THROMBOSIS ( 2 FDA reports)
HUMERUS FRACTURE ( 2 FDA reports)
HYDROURETER ( 2 FDA reports)
HYPERAEMIA ( 2 FDA reports)
HYPERCALCAEMIA OF MALIGNANCY ( 2 FDA reports)
HYPERHIDROSIS ( 2 FDA reports)
HYPOCHROMASIA ( 2 FDA reports)
INFLUENZA ( 2 FDA reports)
INTERNATIONAL NORMALISED RATIO ( 2 FDA reports)
KNEE DEFORMITY ( 2 FDA reports)
LIGAMENT SPRAIN ( 2 FDA reports)
LIP SWELLING ( 2 FDA reports)
LIP ULCERATION ( 2 FDA reports)
LISTLESS ( 2 FDA reports)
LOCALISED INTRAABDOMINAL FLUID COLLECTION ( 2 FDA reports)
LYMPHOCYTE PERCENTAGE DECREASED ( 2 FDA reports)
MALIGNANT MELANOMA ( 2 FDA reports)
MEMORY IMPAIRMENT ( 2 FDA reports)
METABOLIC ACIDOSIS ( 2 FDA reports)
METASTASES TO GASTROINTESTINAL TRACT ( 2 FDA reports)
MOANING ( 2 FDA reports)
MUSCULOSKELETAL STIFFNESS ( 2 FDA reports)
NAIL INFECTION ( 2 FDA reports)
NAIL TOXICITY ( 2 FDA reports)
NEPHROTIC SYNDROME ( 2 FDA reports)
NEURITIS ( 2 FDA reports)
NON-CARDIAC CHEST PAIN ( 2 FDA reports)
NUCLEAR MAGNETIC RESONANCE IMAGING BRAIN ABNORMAL ( 2 FDA reports)
OESOPHAGEAL VARICES HAEMORRHAGE ( 2 FDA reports)
ONYCHALGIA ( 2 FDA reports)
ONYCHOLYSIS ( 2 FDA reports)
ORAL MUCOSAL ERYTHEMA ( 2 FDA reports)
ORAL SOFT TISSUE DISORDER ( 2 FDA reports)
OTOTOXICITY ( 2 FDA reports)
OVARIAN CANCER ( 2 FDA reports)
OVARIAN CANCER METASTATIC ( 2 FDA reports)
OVERDOSE ( 2 FDA reports)
OVERWEIGHT ( 2 FDA reports)
PANCREATIC CARCINOMA METASTATIC ( 2 FDA reports)
PARONYCHIA ( 2 FDA reports)
PEMPHIGOID ( 2 FDA reports)
PERIPHERAL SENSORIMOTOR NEUROPATHY ( 2 FDA reports)
PHARYNGEAL OEDEMA ( 2 FDA reports)
PLATELET COUNT INCREASED ( 2 FDA reports)
PLEURAL FIBROSIS ( 2 FDA reports)
POLYARTHRITIS ( 2 FDA reports)
POLYCHROMIC RED BLOOD CELLS PRESENT ( 2 FDA reports)
PROCEDURAL HYPOTENSION ( 2 FDA reports)
PRURITUS GENERALISED ( 2 FDA reports)
PULSELESS ELECTRICAL ACTIVITY ( 2 FDA reports)
PURULENCE ( 2 FDA reports)
RADIATION OESOPHAGITIS ( 2 FDA reports)
RADIATION SKIN INJURY ( 2 FDA reports)
RED BLOOD CELL SEDIMENTATION RATE INCREASED ( 2 FDA reports)
RED BLOOD CELL TARGET CELLS PRESENT ( 2 FDA reports)
REFLUX OESOPHAGITIS ( 2 FDA reports)
RESPIRATION ABNORMAL ( 2 FDA reports)
SECRETION DISCHARGE ( 2 FDA reports)
SPINAL PAIN ( 2 FDA reports)
SPLENIC GRANULOMA ( 2 FDA reports)
SPUTUM DISCOLOURED ( 2 FDA reports)
STAPHYLOCOCCAL SEPSIS ( 2 FDA reports)
STOMACH DISCOMFORT ( 2 FDA reports)
SYNOVIAL DISORDER ( 2 FDA reports)
TEMPERATURE INTOLERANCE ( 2 FDA reports)
TEMPOROMANDIBULAR JOINT SYNDROME ( 2 FDA reports)
TENDONITIS ( 2 FDA reports)
THERAPEUTIC AGENT TOXICITY ( 2 FDA reports)
THERAPEUTIC RESPONSE DECREASED ( 2 FDA reports)
THERAPEUTIC RESPONSE UNEXPECTED ( 2 FDA reports)
THERAPY CESSATION ( 2 FDA reports)
TRACHEAL OBSTRUCTION ( 2 FDA reports)
TRACHEOMALACIA ( 2 FDA reports)
ULCER ( 2 FDA reports)
URINE KETONE BODY PRESENT ( 2 FDA reports)
URINE LEUKOCYTE ESTERASE POSITIVE ( 2 FDA reports)
UTERINE CANCER ( 2 FDA reports)
VAGINAL DISCHARGE ( 2 FDA reports)
VAGINAL NEOPLASM ( 2 FDA reports)
VENOOCCLUSIVE LIVER DISEASE ( 2 FDA reports)
VENOUS ANEURYSM ( 2 FDA reports)
VENTRICULAR ARRHYTHMIA ( 2 FDA reports)
VENTRICULAR DYSFUNCTION ( 2 FDA reports)
VIRAL INFECTION ( 2 FDA reports)
VOCAL CORD PARESIS ( 2 FDA reports)
VOCAL CORD POLYP ( 2 FDA reports)
VULVAL DISORDER ( 2 FDA reports)
VULVOVAGINAL DISCOMFORT ( 2 FDA reports)
VULVOVAGINAL MYCOTIC INFECTION ( 2 FDA reports)
WAIST CIRCUMFERENCE INCREASED ( 2 FDA reports)
WOUND DEHISCENCE ( 2 FDA reports)
WRONG TECHNIQUE IN DRUG USAGE PROCESS ( 2 FDA reports)
ABDOMINAL INFECTION ( 1 FDA reports)
ABDOMINAL WALL INFECTION ( 1 FDA reports)
ABNORMAL BEHAVIOUR ( 1 FDA reports)
ABSCESS BACTERIAL ( 1 FDA reports)
ACIDOSIS ( 1 FDA reports)
ACTIVATED PARTIAL THROMBOPLASTIN TIME PROLONGED ( 1 FDA reports)
ACUTE HEPATIC FAILURE ( 1 FDA reports)
ACUTE MYELOID LEUKAEMIA ( 1 FDA reports)
ADENOCARCINOMA PANCREAS ( 1 FDA reports)
ADRENAL DISORDER ( 1 FDA reports)
AGGRESSION ( 1 FDA reports)
AGITATION ( 1 FDA reports)
AGONAL RHYTHM ( 1 FDA reports)
ALVEOLAR OSTEITIS ( 1 FDA reports)
ANAPHYLACTOID REACTION ( 1 FDA reports)
ANGINA PECTORIS ( 1 FDA reports)
ANGINA UNSTABLE ( 1 FDA reports)
ANGIOPATHY ( 1 FDA reports)
ANOXIA ( 1 FDA reports)
ANOXIC ENCEPHALOPATHY ( 1 FDA reports)
AORTIC BRUIT ( 1 FDA reports)
AORTIC DISSECTION RUPTURE ( 1 FDA reports)
AORTIC THROMBOSIS ( 1 FDA reports)
APPARENT LIFE THREATENING EVENT ( 1 FDA reports)
APPLICATION SITE ERYTHEMA ( 1 FDA reports)
APPLICATION SITE EXFOLIATION ( 1 FDA reports)
APPLICATION SITE PAIN ( 1 FDA reports)
APPLICATION SITE VESICLES ( 1 FDA reports)
APTYALISM ( 1 FDA reports)
AREFLEXIA ( 1 FDA reports)
ASPHYXIA ( 1 FDA reports)
ATRIAL TACHYCARDIA ( 1 FDA reports)
ATRIOVENTRICULAR BLOCK ( 1 FDA reports)
ATRIOVENTRICULAR BLOCK COMPLETE ( 1 FDA reports)
ATRIOVENTRICULAR BLOCK SECOND DEGREE ( 1 FDA reports)
AXILLARY MASS ( 1 FDA reports)
AZOTAEMIA ( 1 FDA reports)
BACK DISORDER ( 1 FDA reports)
BACTERIA URINE ( 1 FDA reports)
BACTERIAL SEPSIS ( 1 FDA reports)
BALLISMUS ( 1 FDA reports)
BETA HAEMOLYTIC STREPTOCOCCAL INFECTION ( 1 FDA reports)
BILE DUCT OBSTRUCTION ( 1 FDA reports)
BIOPSY SKIN ABNORMAL ( 1 FDA reports)
BLADDER DYSFUNCTION ( 1 FDA reports)
BLADDER NEOPLASM ( 1 FDA reports)
BLOOD CALCIUM INCREASED ( 1 FDA reports)
BLOOD CHLORIDE INCREASED ( 1 FDA reports)
BLOOD CREATINE PHOSPHOKINASE INCREASED ( 1 FDA reports)
BLOOD LACTIC ACID INCREASED ( 1 FDA reports)
BLOOD MAGNESIUM DECREASED ( 1 FDA reports)
BLOOD PH INCREASED ( 1 FDA reports)
BLOODY DISCHARGE ( 1 FDA reports)
BRACHIAL PLEXUS INJURY ( 1 FDA reports)
BRADYCARDIA ( 1 FDA reports)
BRAIN NATRIURETIC PEPTIDE INCREASED ( 1 FDA reports)
BRAIN NEOPLASM ( 1 FDA reports)
BREAST MASS ( 1 FDA reports)
BREAST NEOPLASM ( 1 FDA reports)
BRONCHIAL SECRETION RETENTION ( 1 FDA reports)
BRONCHIAL WALL THICKENING ( 1 FDA reports)
BRONCHOPLEURAL FISTULA ( 1 FDA reports)
BRONCHOSPASM ( 1 FDA reports)
CANCER PAIN ( 1 FDA reports)
CATARACT OPERATION ( 1 FDA reports)
CATHETER RELATED COMPLICATION ( 1 FDA reports)
CATHETER RELATED INFECTION ( 1 FDA reports)
CATHETER SITE DISCHARGE ( 1 FDA reports)
CATHETER SITE EROSION ( 1 FDA reports)
CELLULITIS STAPHYLOCOCCAL ( 1 FDA reports)
CELLULITIS STREPTOCOCCAL ( 1 FDA reports)
CEREBRAL INFARCTION ( 1 FDA reports)
CERVICAL POLYP ( 1 FDA reports)
CHOLANGITIS SCLEROSING ( 1 FDA reports)
CHOREOATHETOSIS ( 1 FDA reports)
CHROMATURIA ( 1 FDA reports)
CLOSTRIDIUM DIFFICILE TOXIN TEST POSITIVE ( 1 FDA reports)
COLD AGGLUTININS POSITIVE ( 1 FDA reports)
COLECTOMY ( 1 FDA reports)
COLLAPSE OF LUNG ( 1 FDA reports)
COLOSTOMY ( 1 FDA reports)
COMA ( 1 FDA reports)
COMPUTERISED TOMOGRAM ABDOMEN ABNORMAL ( 1 FDA reports)
CONJUNCTIVAL IRRITATION ( 1 FDA reports)
CONJUNCTIVAL PALLOR ( 1 FDA reports)
CONJUNCTIVITIS VIRAL ( 1 FDA reports)
COOMBS NEGATIVE HAEMOLYTIC ANAEMIA ( 1 FDA reports)
COOMBS POSITIVE HAEMOLYTIC ANAEMIA ( 1 FDA reports)
CORNEAL ABRASION ( 1 FDA reports)
CORNEAL DECOMPENSATION ( 1 FDA reports)
CORNEAL REFLEX DECREASED ( 1 FDA reports)
CORONARY ARTERY OCCLUSION ( 1 FDA reports)
CORONARY ARTERY THROMBOSIS ( 1 FDA reports)
CRANIAL NERVE DISORDER ( 1 FDA reports)
CREPITATIONS ( 1 FDA reports)
CROHN'S DISEASE ( 1 FDA reports)
CROSS SENSITIVITY REACTION ( 1 FDA reports)
CSF GLUCOSE DECREASED ( 1 FDA reports)
CSF PROTEIN INCREASED ( 1 FDA reports)
CULTURE WOUND POSITIVE ( 1 FDA reports)
DEAFNESS ( 1 FDA reports)
DENTAL TREATMENT ( 1 FDA reports)
DERMATITIS ALLERGIC ( 1 FDA reports)
DERMATITIS EXFOLIATIVE ( 1 FDA reports)
DEVICE DISLOCATION ( 1 FDA reports)
DEVICE FAILURE ( 1 FDA reports)
DEVICE OCCLUSION ( 1 FDA reports)
DIABETES MELLITUS INADEQUATE CONTROL ( 1 FDA reports)
DIAPHRAGMATIC DISORDER ( 1 FDA reports)
DIVERTICULUM INTESTINAL HAEMORRHAGIC ( 1 FDA reports)
DIZZINESS POSTURAL ( 1 FDA reports)
DRUG INTOLERANCE ( 1 FDA reports)
DUODENAL STENOSIS ( 1 FDA reports)
DUODENAL ULCER HAEMORRHAGE ( 1 FDA reports)
DYSPHASIA ( 1 FDA reports)
EAR DISORDER ( 1 FDA reports)
ECTROPION ( 1 FDA reports)
ELECTROCARDIOGRAM ABNORMAL ( 1 FDA reports)
ELECTROCARDIOGRAM CHANGE ( 1 FDA reports)
ELECTROCARDIOGRAM P WAVE ABNORMAL ( 1 FDA reports)
EMBOLIC STROKE ( 1 FDA reports)
EMBOLISM ARTERIAL ( 1 FDA reports)
EMPYEMA DRAINAGE ( 1 FDA reports)
ENCEPHALITIC INFECTION ( 1 FDA reports)
ENCEPHALOPATHY ( 1 FDA reports)
ENDOTOXIC SHOCK ( 1 FDA reports)
ENTERITIS ( 1 FDA reports)
ENTEROCOCCAL INFECTION ( 1 FDA reports)
ENTEROCOLITIS HAEMORRHAGIC ( 1 FDA reports)
EROSIVE DUODENITIS ( 1 FDA reports)
EROSIVE OESOPHAGITIS ( 1 FDA reports)
ERYTHEMA MULTIFORME ( 1 FDA reports)
EXPLORATIVE LAPAROTOMY ( 1 FDA reports)
EYE INFLAMMATION ( 1 FDA reports)
EYE SWELLING ( 1 FDA reports)
EYELID FUNCTION DISORDER ( 1 FDA reports)
FACIAL NERVE DISORDER ( 1 FDA reports)
FAMILY STRESS ( 1 FDA reports)
FEELING OF BODY TEMPERATURE CHANGE ( 1 FDA reports)
FEMUR FRACTURE ( 1 FDA reports)
FISTULA REPAIR ( 1 FDA reports)
FLUID RETENTION ( 1 FDA reports)
FOETOR HEPATICUS ( 1 FDA reports)
FOOD INTOLERANCE ( 1 FDA reports)
FOREIGN BODY TRAUMA ( 1 FDA reports)
GALLBLADDER OPERATION ( 1 FDA reports)
GALLBLADDER POLYP ( 1 FDA reports)
GAMMA BUTYRIC DEHYDROGENASE INCREASED ( 1 FDA reports)
GARDNERELLA INFECTION ( 1 FDA reports)
GASTROINTESTINAL INFLAMMATION ( 1 FDA reports)
GASTROINTESTINAL PAIN ( 1 FDA reports)
GASTROINTESTINAL TOXICITY ( 1 FDA reports)
GASTROINTESTINAL ULCER HAEMORRHAGE ( 1 FDA reports)
GENERAL PHYSICAL CONDITION ABNORMAL ( 1 FDA reports)
GENITAL ULCERATION ( 1 FDA reports)
GILBERT'S SYNDROME ( 1 FDA reports)
GLOBULINS INCREASED ( 1 FDA reports)
GLYCOSYLATED HAEMOGLOBIN INCREASED ( 1 FDA reports)
GRAM STAIN POSITIVE ( 1 FDA reports)
GRANULOCYTOPENIA ( 1 FDA reports)
GROIN INFECTION ( 1 FDA reports)
GUILLAIN-BARRE SYNDROME ( 1 FDA reports)
HAEMARTHROSIS ( 1 FDA reports)
HAEMATOTOXICITY ( 1 FDA reports)
HAEMOGLOBIN INCREASED ( 1 FDA reports)
HAEMOGLOBIN S DECREASED ( 1 FDA reports)
HAEMOLYSIS ( 1 FDA reports)
HAEMORRHAGE URINARY TRACT ( 1 FDA reports)
HEARING DISABILITY ( 1 FDA reports)
HEART RATE DECREASED ( 1 FDA reports)
HEMIANOPIA ( 1 FDA reports)
HEMIPLEGIA ( 1 FDA reports)
HEPATIC ENCEPHALOPATHY ( 1 FDA reports)
HEPATIC FIBROSIS ( 1 FDA reports)
HERPES ZOSTER DISSEMINATED ( 1 FDA reports)
HOSPITALISATION ( 1 FDA reports)
HYPERNATRAEMIA ( 1 FDA reports)
HYPERPHOSPHATAEMIA ( 1 FDA reports)
HYPERREFLEXIA ( 1 FDA reports)
HYPOAESTHESIA EYE ( 1 FDA reports)
HYPOGLYCAEMIC UNCONSCIOUSNESS ( 1 FDA reports)
ILL-DEFINED DISORDER ( 1 FDA reports)
IMPAIRED GASTRIC EMPTYING ( 1 FDA reports)
IMPAIRED WORK ABILITY ( 1 FDA reports)
INAPPROPRIATE SCHEDULE OF DRUG ADMINISTRATION ( 1 FDA reports)
INCOHERENT ( 1 FDA reports)
INCORRECT DOSE ADMINISTERED ( 1 FDA reports)
INCREASED UPPER AIRWAY SECRETION ( 1 FDA reports)
INDURATION ( 1 FDA reports)
INFUSION SITE ERYTHEMA ( 1 FDA reports)
INFUSION SITE EXTRAVASATION ( 1 FDA reports)
INFUSION SITE PAIN ( 1 FDA reports)
INFUSION SITE SWELLING ( 1 FDA reports)
INJECTION SITE PAIN ( 1 FDA reports)
INJECTION SITE SCAR ( 1 FDA reports)
INTESTINAL ISCHAEMIA ( 1 FDA reports)
INTESTINAL POLYP ( 1 FDA reports)
INTRA-ABDOMINAL HAEMATOMA ( 1 FDA reports)
INTRACARDIAC THROMBUS ( 1 FDA reports)
ISCHAEMIC CEREBRAL INFARCTION ( 1 FDA reports)
KERATITIS BACTERIAL ( 1 FDA reports)
KERATOPATHY ( 1 FDA reports)
KETOSIS ( 1 FDA reports)
LAPAROSCOPY ( 1 FDA reports)
LARGE INTESTINAL HAEMORRHAGE ( 1 FDA reports)
LARGE INTESTINE PERFORATION ( 1 FDA reports)
LARYNGOTRACHEAL OEDEMA ( 1 FDA reports)
LEIOMYOMA ( 1 FDA reports)
LEUKOENCEPHALOPATHY ( 1 FDA reports)
LIBIDO DECREASED ( 1 FDA reports)
LIGAMENT DISORDER ( 1 FDA reports)
LIGAMENT RUPTURE ( 1 FDA reports)
LIMB DISCOMFORT ( 1 FDA reports)
LIP DISORDER ( 1 FDA reports)
LISTERIOSIS ( 1 FDA reports)
LIVER INJURY ( 1 FDA reports)
LUNG HYPERINFLATION ( 1 FDA reports)
LYMPHATIC OBSTRUCTION ( 1 FDA reports)
LYMPHATIC SYSTEM NEOPLASM ( 1 FDA reports)
LYMPHOCYTOSIS ( 1 FDA reports)
MASTITIS ( 1 FDA reports)
MEDIASTINAL MASS ( 1 FDA reports)
MEDICATION ERROR ( 1 FDA reports)
METASTASES TO BLADDER ( 1 FDA reports)
METASTASES TO OVARY ( 1 FDA reports)
METASTATIC CARCINOMA OF THE BLADDER ( 1 FDA reports)
METASTATIC MALIGNANT MELANOMA ( 1 FDA reports)
MIGRAINE WITH AURA ( 1 FDA reports)
MITRAL VALVE DISEASE ( 1 FDA reports)
MONOPLEGIA ( 1 FDA reports)
MOOD ALTERED ( 1 FDA reports)
MULTIPLE INJURIES ( 1 FDA reports)
MULTIPLE SCLEROSIS ( 1 FDA reports)
MUSCLE ABSCESS ( 1 FDA reports)
MUSCLE NECROSIS ( 1 FDA reports)
MYOCARDIAL ISCHAEMIA ( 1 FDA reports)
MYOCLONUS ( 1 FDA reports)
NAIL BED BLEEDING ( 1 FDA reports)
NAIL BED DISORDER ( 1 FDA reports)
NAIL DISCOLOURATION ( 1 FDA reports)
NAIL HYPERTROPHY ( 1 FDA reports)
NECROSIS ( 1 FDA reports)
NEURILEMMOMA ( 1 FDA reports)
NEUROLOGICAL DECOMPENSATION ( 1 FDA reports)
NEUTROPHIL COUNT INCREASED ( 1 FDA reports)
NEUTROPHIL PERCENTAGE DECREASED ( 1 FDA reports)
NEUTROPHIL PERCENTAGE INCREASED ( 1 FDA reports)
OBESITY ( 1 FDA reports)
OCULAR HYPERTENSION ( 1 FDA reports)
OESOPHAGEAL CANCER METASTATIC ( 1 FDA reports)
OESOPHAGEAL STENOSIS ( 1 FDA reports)
OESOPHAGEAL ULCER ( 1 FDA reports)
OFF LABEL USE ( 1 FDA reports)
ORAL MUCOSAL BLISTERING ( 1 FDA reports)
ORGANISING PNEUMONIA ( 1 FDA reports)
OVARIAN DISORDER ( 1 FDA reports)
OVARIAN EPITHELIAL CANCER ( 1 FDA reports)
PALLOR ( 1 FDA reports)
PANCREATITIS ACUTE ( 1 FDA reports)
PARAESTHESIA ORAL ( 1 FDA reports)
PARANEOPLASTIC SYNDROME ( 1 FDA reports)
PARESIS ( 1 FDA reports)
PARTIAL SEIZURES ( 1 FDA reports)
PATHOGEN RESISTANCE ( 1 FDA reports)
PCO2 DECREASED ( 1 FDA reports)
PCO2 INCREASED ( 1 FDA reports)
PELVIC ABSCESS ( 1 FDA reports)
PERFORMANCE STATUS DECREASED ( 1 FDA reports)
PERITONEAL FLUID ANALYSIS ABNORMAL ( 1 FDA reports)
PLASTIC SURGERY TO THE FACE ( 1 FDA reports)
PLATELET COUNT ABNORMAL ( 1 FDA reports)
PLEURISY ( 1 FDA reports)
PNEUMONIA KLEBSIELLA ( 1 FDA reports)
PO2 DECREASED ( 1 FDA reports)
PO2 INCREASED ( 1 FDA reports)
POLYNEUROPATHY ( 1 FDA reports)
POLYP ( 1 FDA reports)
PORTAL VEIN OCCLUSION ( 1 FDA reports)
POSTERIOR CAPSULE OPACIFICATION ( 1 FDA reports)
POSTOPERATIVE ABSCESS ( 1 FDA reports)
POSTOPERATIVE ADHESION ( 1 FDA reports)
POUCHITIS ( 1 FDA reports)
PRESBYOPIA ( 1 FDA reports)
PROCEDURAL PAIN ( 1 FDA reports)
PROTHROMBIN TIME SHORTENED ( 1 FDA reports)
PULMONARY HAEMORRHAGE ( 1 FDA reports)
PULMONARY MYCOSIS ( 1 FDA reports)
PULMONARY TOXICITY ( 1 FDA reports)
PULMONARY VASCULAR DISORDER ( 1 FDA reports)
PULSE ABSENT ( 1 FDA reports)
PUPILLARY DISORDER ( 1 FDA reports)
PUPILLARY REFLEX IMPAIRED ( 1 FDA reports)
PYELONEPHRITIS ACUTE ( 1 FDA reports)
RADIATION ASSOCIATED PAIN ( 1 FDA reports)
RADIATION MUCOSITIS ( 1 FDA reports)
RADIOTHERAPY TO BONE ( 1 FDA reports)
RECALL PHENOMENON ( 1 FDA reports)
RECTAL ABSCESS ( 1 FDA reports)
RED CELL DISTRIBUTION WIDTH DECREASED ( 1 FDA reports)
RED CELL DISTRIBUTION WIDTH INCREASED ( 1 FDA reports)
REFRACTION DISORDER ( 1 FDA reports)
RESPIRATORY ACIDOSIS ( 1 FDA reports)
RESPIRATORY RATE DECREASED ( 1 FDA reports)
RETINAL VASCULAR DISORDER ( 1 FDA reports)
RETROPERITONEAL LYMPHADENOPATHY ( 1 FDA reports)
REVERSIBLE POSTERIOR LEUKOENCEPHALOPATHY SYNDROME ( 1 FDA reports)
RIGHT VENTRICULAR DYSFUNCTION ( 1 FDA reports)
SALIVARY HYPERSECRETION ( 1 FDA reports)
SCAB ( 1 FDA reports)
SCLERAL CYST ( 1 FDA reports)
SENSATION OF HEAVINESS ( 1 FDA reports)
SEROMA ( 1 FDA reports)
SHOULDER PAIN ( 1 FDA reports)
SIGMOIDITIS ( 1 FDA reports)
SIMPLEX VIRUS TEST POSITIVE ( 1 FDA reports)
SINUS HEADACHE ( 1 FDA reports)
SKIN GRAFT ( 1 FDA reports)
SKIN GRAFT FAILURE ( 1 FDA reports)
SKIN HAEMORRHAGE ( 1 FDA reports)
SKIN HYPERPIGMENTATION ( 1 FDA reports)
SKIN NECROSIS ( 1 FDA reports)
SKIN NEOPLASM EXCISION ( 1 FDA reports)
SKIN ULCER HAEMORRHAGE ( 1 FDA reports)
SKIN WARM ( 1 FDA reports)
SMALL INTESTINE CARCINOMA RECURRENT ( 1 FDA reports)
SOFT TISSUE MASS ( 1 FDA reports)
SOFT TISSUE NECROSIS ( 1 FDA reports)
SPINAL CORD INFARCTION ( 1 FDA reports)
SPUTUM CULTURE POSITIVE ( 1 FDA reports)
STARING ( 1 FDA reports)
STARVATION ( 1 FDA reports)
STENOTROPHOMONAS INFECTION ( 1 FDA reports)
STREPTOCOCCUS TEST POSITIVE ( 1 FDA reports)
STRIDOR ( 1 FDA reports)
SUBCUTANEOUS NODULE ( 1 FDA reports)
SUDDEN HEARING LOSS ( 1 FDA reports)
SURGERY ( 1 FDA reports)
TANDEM GAIT TEST ABNORMAL ( 1 FDA reports)
THERAPY NON-RESPONDER ( 1 FDA reports)
THROAT TIGHTNESS ( 1 FDA reports)
THROMBOSIS IN DEVICE ( 1 FDA reports)
THYROIDITIS ( 1 FDA reports)
THYROXINE FREE DECREASED ( 1 FDA reports)
TIC ( 1 FDA reports)
TINNITUS ( 1 FDA reports)
TOOTH SOCKET HAEMORRHAGE ( 1 FDA reports)
TORSADE DE POINTES ( 1 FDA reports)
TOXICITY TO VARIOUS AGENTS ( 1 FDA reports)
TRACHEITIS ( 1 FDA reports)
TRANSAMINASES ( 1 FDA reports)
TRANSIENT ISCHAEMIC ATTACK ( 1 FDA reports)
TREATMENT FAILURE ( 1 FDA reports)
TREATMENT NONCOMPLIANCE ( 1 FDA reports)
TRICHIASIS ( 1 FDA reports)
TROPONIN INCREASED ( 1 FDA reports)
TUMOUR COMPRESSION ( 1 FDA reports)
TUMOUR EMBOLISM ( 1 FDA reports)
TUMOUR HAEMORRHAGE ( 1 FDA reports)
TUMOUR PAIN ( 1 FDA reports)
TUMOUR THROMBOSIS ( 1 FDA reports)
TYPE 2 DIABETES MELLITUS ( 1 FDA reports)
TYPE IV HYPERSENSITIVITY REACTION ( 1 FDA reports)
URINARY TRACT INFECTION BACTERIAL ( 1 FDA reports)
URINE ODOUR ABNORMAL ( 1 FDA reports)
VARICES OESOPHAGEAL ( 1 FDA reports)
VENOUS THROMBOSIS ( 1 FDA reports)
VENOUS THROMBOSIS LIMB ( 1 FDA reports)
VENTRICULAR EXTRASYSTOLES ( 1 FDA reports)
VENTRICULAR HYPOKINESIA ( 1 FDA reports)
VERTIGO ( 1 FDA reports)
VITAMIN B12 INCREASED ( 1 FDA reports)
VITREOUS DEGENERATION ( 1 FDA reports)
VULVA INJURY ( 1 FDA reports)
VULVOVAGINAL DRYNESS ( 1 FDA reports)
VULVOVAGINAL PAIN ( 1 FDA reports)
WEIGHT BEARING DIFFICULTY ( 1 FDA reports)
WRONG DRUG ADMINISTERED ( 1 FDA reports)

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