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

NAUSEA ( 394 FDA reports)
DYSPNOEA ( 291 FDA reports)
VOMITING ( 287 FDA reports)
PAIN ( 281 FDA reports)
ANAEMIA ( 264 FDA reports)
DEHYDRATION ( 246 FDA reports)
FATIGUE ( 238 FDA reports)
DIARRHOEA ( 218 FDA reports)
ANXIETY ( 200 FDA reports)
BACK PAIN ( 200 FDA reports)
PYREXIA ( 173 FDA reports)
OSTEONECROSIS OF JAW ( 171 FDA reports)
HEADACHE ( 162 FDA reports)
DECREASED APPETITE ( 157 FDA reports)
PLEURAL EFFUSION ( 152 FDA reports)
PNEUMONIA ( 146 FDA reports)
HYPOTENSION ( 145 FDA reports)
BONE DISORDER ( 143 FDA reports)
CHEST PAIN ( 140 FDA reports)
DEATH ( 133 FDA reports)
PAIN IN EXTREMITY ( 131 FDA reports)
ERYTHEMA ( 129 FDA reports)
HYPOAESTHESIA ( 129 FDA reports)
RASH ( 128 FDA reports)
PARAESTHESIA ( 127 FDA reports)
CONSTIPATION ( 126 FDA reports)
ABDOMINAL PAIN ( 124 FDA reports)
OEDEMA PERIPHERAL ( 123 FDA reports)
ASTHENIA ( 121 FDA reports)
RENAL FAILURE ACUTE ( 121 FDA reports)
NEUROPATHY PERIPHERAL ( 117 FDA reports)
DIZZINESS ( 116 FDA reports)
WEIGHT DECREASED ( 116 FDA reports)
METASTASES TO BONE ( 111 FDA reports)
INJURY ( 105 FDA reports)
SPINAL OSTEOARTHRITIS ( 105 FDA reports)
TOOTH EXTRACTION ( 105 FDA reports)
FLUSHING ( 104 FDA reports)
MALIGNANT NEOPLASM PROGRESSION ( 100 FDA reports)
ARTHRALGIA ( 99 FDA reports)
NEUTROPENIA ( 99 FDA reports)
BONE PAIN ( 97 FDA reports)
PLATELET COUNT DECREASED ( 97 FDA reports)
FEBRILE NEUTROPENIA ( 95 FDA reports)
INFECTION ( 95 FDA reports)
WHITE BLOOD CELL COUNT DECREASED ( 94 FDA reports)
THROMBOCYTOPENIA ( 91 FDA reports)
GENERAL PHYSICAL HEALTH DETERIORATION ( 90 FDA reports)
HAEMOGLOBIN DECREASED ( 90 FDA reports)
COUGH ( 89 FDA reports)
HYPERSENSITIVITY ( 89 FDA reports)
OSTEOMYELITIS ( 89 FDA reports)
HAEMORRHOIDS ( 87 FDA reports)
OSTEOARTHRITIS ( 87 FDA reports)
OSTEONECROSIS ( 87 FDA reports)
SYNCOPE ( 87 FDA reports)
PRURITUS ( 86 FDA reports)
STOMATITIS ( 86 FDA reports)
CHEST DISCOMFORT ( 85 FDA reports)
DECREASED INTEREST ( 85 FDA reports)
HYPOKALAEMIA ( 85 FDA reports)
SEPSIS ( 85 FDA reports)
PAIN IN JAW ( 84 FDA reports)
DYSPHAGIA ( 81 FDA reports)
EMOTIONAL DISTRESS ( 80 FDA reports)
SWELLING ( 80 FDA reports)
FALL ( 79 FDA reports)
PANCYTOPENIA ( 79 FDA reports)
DEFORMITY ( 78 FDA reports)
MALAISE ( 75 FDA reports)
CHILLS ( 74 FDA reports)
OSTEOPOROSIS ( 74 FDA reports)
SINUSITIS ( 74 FDA reports)
HYPERTENSION ( 73 FDA reports)
MOUTH ULCERATION ( 73 FDA reports)
DEEP VEIN THROMBOSIS ( 72 FDA reports)
LYMPHADENOPATHY ( 72 FDA reports)
BLOOD PRESSURE INCREASED ( 71 FDA reports)
GAIT DISTURBANCE ( 71 FDA reports)
TOOTH DISORDER ( 71 FDA reports)
DEPRESSION ( 70 FDA reports)
INTERVERTEBRAL DISC PROTRUSION ( 70 FDA reports)
PULMONARY EMBOLISM ( 70 FDA reports)
BRONCHITIS ( 69 FDA reports)
METASTASES TO LUNG ( 69 FDA reports)
INTERVERTEBRAL DISC DEGENERATION ( 68 FDA reports)
URINARY TRACT INFECTION ( 66 FDA reports)
BONE LESION ( 64 FDA reports)
CONFUSIONAL STATE ( 63 FDA reports)
NEOPLASM MALIGNANT ( 62 FDA reports)
HYPOAESTHESIA ORAL ( 61 FDA reports)
MENTAL STATUS CHANGES ( 61 FDA reports)
VISION BLURRED ( 61 FDA reports)
IMPAIRED HEALING ( 60 FDA reports)
INFUSION RELATED REACTION ( 60 FDA reports)
BLOOD CREATININE INCREASED ( 59 FDA reports)
OSTEOPENIA ( 59 FDA reports)
CELLULITIS ( 58 FDA reports)
CONVULSION ( 58 FDA reports)
DERMATITIS ACNEIFORM ( 58 FDA reports)
DYSURIA ( 57 FDA reports)
INTERSTITIAL LUNG DISEASE ( 57 FDA reports)
GASTROOESOPHAGEAL REFLUX DISEASE ( 56 FDA reports)
HYPOPHAGIA ( 56 FDA reports)
LOSS OF CONSCIOUSNESS ( 56 FDA reports)
ALOPECIA ( 55 FDA reports)
BLOOD GLUCOSE INCREASED ( 55 FDA reports)
DYSARTHRIA ( 54 FDA reports)
METASTASES TO SPINE ( 54 FDA reports)
NECK PAIN ( 54 FDA reports)
DRUG INEFFECTIVE ( 52 FDA reports)
NEUTROPHIL COUNT DECREASED ( 52 FDA reports)
HYPOXIA ( 51 FDA reports)
METASTASES TO LIVER ( 51 FDA reports)
ATRIAL FIBRILLATION ( 50 FDA reports)
MUSCLE SPASMS ( 49 FDA reports)
MUSCULAR WEAKNESS ( 49 FDA reports)
TRICUSPID VALVE INCOMPETENCE ( 49 FDA reports)
DENTAL CARIES ( 48 FDA reports)
ORAL PAIN ( 48 FDA reports)
METASTASES TO CENTRAL NERVOUS SYSTEM ( 47 FDA reports)
INSOMNIA ( 45 FDA reports)
MASS ( 45 FDA reports)
MUCOSAL INFLAMMATION ( 45 FDA reports)
RESPIRATORY FAILURE ( 45 FDA reports)
CARDIAC ARREST ( 44 FDA reports)
DEBRIDEMENT ( 44 FDA reports)
HAEMATURIA ( 44 FDA reports)
HIATUS HERNIA ( 44 FDA reports)
HYPOPHOSPHATAEMIA ( 44 FDA reports)
LEUKOPENIA ( 44 FDA reports)
NEPHROLITHIASIS ( 44 FDA reports)
BLOOD ALKALINE PHOSPHATASE INCREASED ( 43 FDA reports)
HYPOMAGNESAEMIA ( 43 FDA reports)
RENAL CYST ( 43 FDA reports)
TACHYCARDIA ( 43 FDA reports)
ATELECTASIS ( 42 FDA reports)
WHITE BLOOD CELL COUNT INCREASED ( 42 FDA reports)
HYPOCALCAEMIA ( 41 FDA reports)
OEDEMA ( 41 FDA reports)
BONE DEBRIDEMENT ( 40 FDA reports)
SCOLIOSIS ( 40 FDA reports)
DYSPNOEA EXERTIONAL ( 39 FDA reports)
HAEMORRHAGE ( 39 FDA reports)
OSTEOSCLEROSIS ( 39 FDA reports)
RED BLOOD CELL COUNT DECREASED ( 39 FDA reports)
ABDOMINAL PAIN UPPER ( 38 FDA reports)
BLOOD PRESSURE DECREASED ( 38 FDA reports)
HYPERHIDROSIS ( 38 FDA reports)
LUNG NEOPLASM ( 38 FDA reports)
MITRAL VALVE INCOMPETENCE ( 38 FDA reports)
BREAST CANCER METASTATIC ( 37 FDA reports)
HAEMOPTYSIS ( 37 FDA reports)
HYPERKALAEMIA ( 37 FDA reports)
OXYGEN SATURATION DECREASED ( 37 FDA reports)
ANAPHYLACTIC REACTION ( 36 FDA reports)
CENTRAL VENOUS CATHETERISATION ( 36 FDA reports)
SEPTIC SHOCK ( 36 FDA reports)
CARDIAC FAILURE CONGESTIVE ( 35 FDA reports)
LUNG INFILTRATION ( 35 FDA reports)
RENAL FAILURE ( 35 FDA reports)
SWELLING FACE ( 35 FDA reports)
ARTHROPATHY ( 34 FDA reports)
DEVICE RELATED INFECTION ( 34 FDA reports)
DRY SKIN ( 34 FDA reports)
EAR PAIN ( 34 FDA reports)
MASTECTOMY ( 34 FDA reports)
MULTI-ORGAN FAILURE ( 34 FDA reports)
ANHEDONIA ( 33 FDA reports)
FEELING ABNORMAL ( 33 FDA reports)
PERIODONTAL DISEASE ( 33 FDA reports)
RECTAL HAEMORRHAGE ( 33 FDA reports)
RESPIRATORY DISTRESS ( 33 FDA reports)
TREMOR ( 33 FDA reports)
BONE NEOPLASM MALIGNANT ( 32 FDA reports)
CARDIO-RESPIRATORY ARREST ( 32 FDA reports)
HAEMATOCRIT DECREASED ( 32 FDA reports)
HEPATIC FAILURE ( 32 FDA reports)
HYPONATRAEMIA ( 32 FDA reports)
MUSCULOSKELETAL CHEST PAIN ( 32 FDA reports)
PRIMARY SEQUESTRUM ( 32 FDA reports)
SEQUESTRECTOMY ( 32 FDA reports)
UPPER RESPIRATORY TRACT INFECTION ( 32 FDA reports)
CYST ( 31 FDA reports)
HEART RATE INCREASED ( 31 FDA reports)
KYPHOSIS ( 31 FDA reports)
OESOPHAGITIS ( 31 FDA reports)
ASCITES ( 30 FDA reports)
LUMBAR SPINAL STENOSIS ( 30 FDA reports)
ROTATOR CUFF SYNDROME ( 30 FDA reports)
TONGUE ULCERATION ( 30 FDA reports)
TOOTHACHE ( 30 FDA reports)
BACTERAEMIA ( 29 FDA reports)
COAGULOPATHY ( 29 FDA reports)
HYDRONEPHROSIS ( 29 FDA reports)
LUNG DISORDER ( 29 FDA reports)
LYMPHADENOPATHY MEDIASTINAL ( 29 FDA reports)
SLEEP APNOEA SYNDROME ( 29 FDA reports)
URTICARIA ( 29 FDA reports)
ABSCESS ( 28 FDA reports)
CHRONIC OBSTRUCTIVE PULMONARY DISEASE ( 28 FDA reports)
LIBIDO DECREASED ( 28 FDA reports)
LYMPHOEDEMA ( 28 FDA reports)
MYOCARDIAL INFARCTION ( 28 FDA reports)
RENAL FAILURE CHRONIC ( 28 FDA reports)
CERVICAL SPINAL STENOSIS ( 27 FDA reports)
CONDITION AGGRAVATED ( 27 FDA reports)
OSTEOLYSIS ( 27 FDA reports)
TOOTH IMPACTED ( 27 FDA reports)
ARTERIOSCLEROSIS ( 26 FDA reports)
BLOOD CALCIUM DECREASED ( 26 FDA reports)
CATARACT ( 26 FDA reports)
DISCOMFORT ( 26 FDA reports)
LEFT ATRIAL DILATATION ( 26 FDA reports)
MALNUTRITION ( 26 FDA reports)
ORAL CANDIDIASIS ( 26 FDA reports)
PALMAR-PLANTAR ERYTHRODYSAESTHESIA SYNDROME ( 26 FDA reports)
ACUTE RESPIRATORY FAILURE ( 25 FDA reports)
BONE MARROW FAILURE ( 25 FDA reports)
HYPERKERATOSIS ( 25 FDA reports)
INFLAMMATION ( 25 FDA reports)
MYOFASCIAL PAIN SYNDROME ( 25 FDA reports)
NECK MASS ( 25 FDA reports)
PNEUMONIA ASPIRATION ( 25 FDA reports)
RENAL TUBULAR NECROSIS ( 25 FDA reports)
SOMNOLENCE ( 25 FDA reports)
SUPRAVENTRICULAR TACHYCARDIA ( 25 FDA reports)
ABSCESS DRAINAGE ( 24 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 24 FDA reports)
CONTUSION ( 24 FDA reports)
DEPRESSED MOOD ( 24 FDA reports)
DYSGEUSIA ( 24 FDA reports)
ENDODONTIC PROCEDURE ( 24 FDA reports)
EXPOSED BONE IN JAW ( 24 FDA reports)
FEELING HOT ( 24 FDA reports)
HYPERCALCAEMIA ( 24 FDA reports)
HYPOVOLAEMIA ( 24 FDA reports)
LEFT VENTRICULAR HYPERTROPHY ( 24 FDA reports)
MELAENA ( 24 FDA reports)
MOOD SWINGS ( 24 FDA reports)
ORAL INFECTION ( 24 FDA reports)
PALPITATIONS ( 24 FDA reports)
PULMONARY FIBROSIS ( 24 FDA reports)
SPINAL COLUMN STENOSIS ( 24 FDA reports)
TOOTH FRACTURE ( 24 FDA reports)
TOOTH REPAIR ( 24 FDA reports)
VERTEBROPLASTY ( 24 FDA reports)
ACTINOMYCOSIS ( 23 FDA reports)
ANOREXIA ( 23 FDA reports)
APHASIA ( 23 FDA reports)
BLOOD LACTATE DEHYDROGENASE INCREASED ( 23 FDA reports)
COMPUTERISED TOMOGRAM ABNORMAL ( 23 FDA reports)
DEPRESSED LEVEL OF CONSCIOUSNESS ( 23 FDA reports)
DISABILITY ( 23 FDA reports)
DISEASE PROGRESSION ( 23 FDA reports)
FAECES DISCOLOURED ( 23 FDA reports)
GINGIVAL ULCERATION ( 23 FDA reports)
GLOSSODYNIA ( 23 FDA reports)
ILEUS ( 23 FDA reports)
LETHARGY ( 23 FDA reports)
MOUTH HAEMORRHAGE ( 23 FDA reports)
ANAPHYLACTIC SHOCK ( 22 FDA reports)
DENTAL FISTULA ( 22 FDA reports)
ECCHYMOSIS ( 22 FDA reports)
FISTULA ( 22 FDA reports)
HAND-FOOT-AND-MOUTH DISEASE ( 22 FDA reports)
HIP FRACTURE ( 22 FDA reports)
HYPERGLYCAEMIA ( 22 FDA reports)
LOOSE TOOTH ( 22 FDA reports)
POLYARTHRITIS ( 22 FDA reports)
SINUS DISORDER ( 22 FDA reports)
TRANSIENT ISCHAEMIC ATTACK ( 22 FDA reports)
UNRESPONSIVE TO STIMULI ( 22 FDA reports)
WHEEZING ( 22 FDA reports)
AORTIC ARTERIOSCLEROSIS ( 21 FDA reports)
BALANCE DISORDER ( 21 FDA reports)
BLOOD POTASSIUM DECREASED ( 21 FDA reports)
BONE DENSITY DECREASED ( 21 FDA reports)
BONE TRIMMING ( 21 FDA reports)
BRADYCARDIA ( 21 FDA reports)
CHOLELITHIASIS ( 21 FDA reports)
DISSEMINATED INTRAVASCULAR COAGULATION ( 21 FDA reports)
HERPES ZOSTER ( 21 FDA reports)
METABOLIC ACIDOSIS ( 21 FDA reports)
NODULE ( 21 FDA reports)
OSTEOMYELITIS CHRONIC ( 21 FDA reports)
PALLOR ( 21 FDA reports)
RASH GENERALISED ( 21 FDA reports)
SPINAL COMPRESSION FRACTURE ( 21 FDA reports)
URINARY INCONTINENCE ( 21 FDA reports)
ASPIRATION PLEURAL CAVITY ( 20 FDA reports)
BRAIN CANCER METASTATIC ( 20 FDA reports)
BRAIN OEDEMA ( 20 FDA reports)
BREAST MASS ( 20 FDA reports)
CENTRAL VENOUS CATHETER REMOVAL ( 20 FDA reports)
CYSTITIS ( 20 FDA reports)
DENTAL OPERATION ( 20 FDA reports)
DIVERTICULUM ( 20 FDA reports)
EPISTAXIS ( 20 FDA reports)
FLUID RETENTION ( 20 FDA reports)
GINGIVAL BLEEDING ( 20 FDA reports)
GLAUCOMA ( 20 FDA reports)
HEPATIC CANCER METASTATIC ( 20 FDA reports)
MUSCULOSKELETAL PAIN ( 20 FDA reports)
OVARIAN CYST ( 20 FDA reports)
PHYSICAL DISABILITY ( 20 FDA reports)
POLYP ( 20 FDA reports)
RETCHING ( 20 FDA reports)
SEBORRHOEIC KERATOSIS ( 20 FDA reports)
WEIGHT INCREASED ( 20 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 19 FDA reports)
AMNESIA ( 19 FDA reports)
ATAXIA ( 19 FDA reports)
CANDIDIASIS ( 19 FDA reports)
CEREBRAL ATROPHY ( 19 FDA reports)
DRUG HYPERSENSITIVITY ( 19 FDA reports)
EJECTION FRACTION DECREASED ( 19 FDA reports)
GINGIVAL PAIN ( 19 FDA reports)
HYPERLIPIDAEMIA ( 19 FDA reports)
INTESTINAL ISCHAEMIA ( 19 FDA reports)
MUSCLE TWITCHING ( 19 FDA reports)
MYALGIA ( 19 FDA reports)
MYELODYSPLASTIC SYNDROME ( 19 FDA reports)
PANCREATIC CYST ( 19 FDA reports)
RADICULOPATHY ( 19 FDA reports)
SLEEP DISORDER ( 19 FDA reports)
TOOTH ABSCESS ( 19 FDA reports)
TOOTH INFECTION ( 19 FDA reports)
ADENOCARCINOMA ( 18 FDA reports)
ANGINA PECTORIS ( 18 FDA reports)
BLOOD POTASSIUM INCREASED ( 18 FDA reports)
CEREBRAL INFARCTION ( 18 FDA reports)
CHRONIC SINUSITIS ( 18 FDA reports)
FUNGAL INFECTION ( 18 FDA reports)
GASTROINTESTINAL HAEMORRHAGE ( 18 FDA reports)
GINGIVAL INFECTION ( 18 FDA reports)
LYMPHOMA ( 18 FDA reports)
POLLAKIURIA ( 18 FDA reports)
PULMONARY VALVE INCOMPETENCE ( 18 FDA reports)
BREAST CANCER ( 17 FDA reports)
CATHETER RELATED INFECTION ( 17 FDA reports)
COLORECTAL CANCER ( 17 FDA reports)
HAEMATOMA ( 17 FDA reports)
HAEMORRHAGE INTRACRANIAL ( 17 FDA reports)
HEMIPARESIS ( 17 FDA reports)
LEUKOCYTOSIS ( 17 FDA reports)
ORAL DISORDER ( 17 FDA reports)
PETECHIAE ( 17 FDA reports)
PRODUCTIVE COUGH ( 17 FDA reports)
PROTHROMBIN TIME PROLONGED ( 17 FDA reports)
RENAL ATROPHY ( 17 FDA reports)
RESPIRATORY ARREST ( 17 FDA reports)
SKIN DISORDER ( 17 FDA reports)
TOOTH LOSS ( 17 FDA reports)
WOUND DEHISCENCE ( 17 FDA reports)
BRONCHIECTASIS ( 16 FDA reports)
CARDIOMEGALY ( 16 FDA reports)
CLOSTRIDIUM DIFFICILE COLITIS ( 16 FDA reports)
EXOSTOSIS ( 16 FDA reports)
EXTRAVASATION ( 16 FDA reports)
FACET JOINT SYNDROME ( 16 FDA reports)
GINGIVITIS ( 16 FDA reports)
LOCALISED OEDEMA ( 16 FDA reports)
METASTATIC NEOPLASM ( 16 FDA reports)
MYOCARDIAL ISCHAEMIA ( 16 FDA reports)
NASOPHARYNGITIS ( 16 FDA reports)
PARKINSON'S DISEASE ( 16 FDA reports)
PATHOLOGICAL FRACTURE ( 16 FDA reports)
RASH ERYTHEMATOUS ( 16 FDA reports)
SINUS TACHYCARDIA ( 16 FDA reports)
SPEECH DISORDER ( 16 FDA reports)
TRANSFUSION ( 16 FDA reports)
ABDOMINAL DISTENSION ( 15 FDA reports)
AORTIC VALVE INCOMPETENCE ( 15 FDA reports)
BLOOD UREA INCREASED ( 15 FDA reports)
BONE FRAGMENTATION ( 15 FDA reports)
CARDIOMYOPATHY ( 15 FDA reports)
CERVICOBRACHIAL SYNDROME ( 15 FDA reports)
CONJUNCTIVITIS ( 15 FDA reports)
EOSINOPHIL COUNT DECREASED ( 15 FDA reports)
FEMUR FRACTURE ( 15 FDA reports)
GINGIVAL ATROPHY ( 15 FDA reports)
GLOBULINS INCREASED ( 15 FDA reports)
HAEMATOCHEZIA ( 15 FDA reports)
HEPATIC LESION ( 15 FDA reports)
HEPATOMEGALY ( 15 FDA reports)
INJECTION SITE PAIN ( 15 FDA reports)
INTERVERTEBRAL DISC SPACE NARROWING ( 15 FDA reports)
JAUNDICE ( 15 FDA reports)
LIMB INJURY ( 15 FDA reports)
LUNG HYPERINFLATION ( 15 FDA reports)
LYMPHOCYTE COUNT DECREASED ( 15 FDA reports)
NEOPLASM PROGRESSION ( 15 FDA reports)
NEUTROPHIL COUNT INCREASED ( 15 FDA reports)
OBSTRUCTION GASTRIC ( 15 FDA reports)
OBSTRUCTIVE AIRWAYS DISORDER ( 15 FDA reports)
ORAL HERPES ( 15 FDA reports)
ORTHOSTATIC HYPOTENSION ( 15 FDA reports)
OVERDOSE ( 15 FDA reports)
PANCREATITIS ( 15 FDA reports)
PARONYCHIA ( 15 FDA reports)
PROCTITIS ( 15 FDA reports)
SENSORY DISTURBANCE ( 15 FDA reports)
SKIN CANCER ( 15 FDA reports)
THROAT TIGHTNESS ( 15 FDA reports)
ACNE ( 14 FDA reports)
ADENOMA BENIGN ( 14 FDA reports)
ALBUMIN GLOBULIN RATIO DECREASED ( 14 FDA reports)
BLOOD MAGNESIUM DECREASED ( 14 FDA reports)
BLOOD SODIUM DECREASED ( 14 FDA reports)
CEREBROVASCULAR ACCIDENT ( 14 FDA reports)
DIALYSIS ( 14 FDA reports)
DYSPEPSIA ( 14 FDA reports)
GAMMA-GLUTAMYLTRANSFERASE INCREASED ( 14 FDA reports)
GENERALISED OEDEMA ( 14 FDA reports)
HAEMANGIOMA ( 14 FDA reports)
INTESTINAL PERFORATION ( 14 FDA reports)
JAW DISORDER ( 14 FDA reports)
LEUKODYSTROPHY ( 14 FDA reports)
LIFE EXPECTANCY SHORTENED ( 14 FDA reports)
LOCAL SWELLING ( 14 FDA reports)
LYMPH NODE PALPABLE ( 14 FDA reports)
MENINGITIS ( 14 FDA reports)
MONOCYTE COUNT DECREASED ( 14 FDA reports)
NIGHT SWEATS ( 14 FDA reports)
NUCLEAR MAGNETIC RESONANCE IMAGING ABNORMAL ( 14 FDA reports)
OESOPHAGEAL PAIN ( 14 FDA reports)
ORAL INTAKE REDUCED ( 14 FDA reports)
PERIODONTITIS ( 14 FDA reports)
PULMONARY MASS ( 14 FDA reports)
RENAL IMPAIRMENT ( 14 FDA reports)
RIB FRACTURE ( 14 FDA reports)
SKIN DISCOLOURATION ( 14 FDA reports)
SKIN EXFOLIATION ( 14 FDA reports)
SPINAL DISORDER ( 14 FDA reports)
SPLENOMEGALY ( 14 FDA reports)
SUBDURAL HAEMATOMA ( 14 FDA reports)
THROMBOTIC THROMBOCYTOPENIC PURPURA ( 14 FDA reports)
UPPER GASTROINTESTINAL HAEMORRHAGE ( 14 FDA reports)
ACTINIC KERATOSIS ( 13 FDA reports)
ACTIVITIES OF DAILY LIVING IMPAIRED ( 13 FDA reports)
APPENDICITIS ( 13 FDA reports)
BREAST RECONSTRUCTION ( 13 FDA reports)
CENTRAL NERVOUS SYSTEM LESION ( 13 FDA reports)
COLITIS ( 13 FDA reports)
COMPRESSION FRACTURE ( 13 FDA reports)
DENTURE WEARER ( 13 FDA reports)
DERMAL CYST ( 13 FDA reports)
DRUG EFFECT DECREASED ( 13 FDA reports)
DYSPHONIA ( 13 FDA reports)
EYE SWELLING ( 13 FDA reports)
FAECAL INCONTINENCE ( 13 FDA reports)
GASTROENTERITIS VIRAL ( 13 FDA reports)
GOITRE ( 13 FDA reports)
HYPERCHOLESTEROLAEMIA ( 13 FDA reports)
JOINT INJURY ( 13 FDA reports)
JOINT SWELLING ( 13 FDA reports)
LICHEN PLANUS ( 13 FDA reports)
MAXILLOFACIAL OPERATION ( 13 FDA reports)
OSTEORADIONECROSIS ( 13 FDA reports)
PARAESTHESIA ORAL ( 13 FDA reports)
PNEUMONITIS ( 13 FDA reports)
RESTLESS LEGS SYNDROME ( 13 FDA reports)
SCAR ( 13 FDA reports)
SKIN ULCER ( 13 FDA reports)
SPONDYLITIC MYELOPATHY ( 13 FDA reports)
STEM CELL TRANSPLANT ( 13 FDA reports)
TONGUE DISCOLOURATION ( 13 FDA reports)
VITAMIN B12 DEFICIENCY ( 13 FDA reports)
APPENDICITIS PERFORATED ( 12 FDA reports)
BIOPSY BREAST ABNORMAL ( 12 FDA reports)
BIOPSY LYMPH GLAND ( 12 FDA reports)
BLINDNESS TRANSIENT ( 12 FDA reports)
BONE SCAN ABNORMAL ( 12 FDA reports)
BREAST CANCER FEMALE ( 12 FDA reports)
BREAST PROSTHESIS REMOVAL ( 12 FDA reports)
BREAST PROSTHESIS USER ( 12 FDA reports)
CARPAL TUNNEL SYNDROME ( 12 FDA reports)
EUSTACHIAN TUBE DYSFUNCTION ( 12 FDA reports)
FIBROMYALGIA ( 12 FDA reports)
FLANK PAIN ( 12 FDA reports)
GLOMERULAR FILTRATION RATE DECREASED ( 12 FDA reports)
GOUTY ARTHRITIS ( 12 FDA reports)
HEAD INJURY ( 12 FDA reports)
HEART RATE IRREGULAR ( 12 FDA reports)
HEPATIC NEOPLASM MALIGNANT ( 12 FDA reports)
HORDEOLUM ( 12 FDA reports)
HYPERREFLEXIA ( 12 FDA reports)
IRON DEFICIENCY ( 12 FDA reports)
LEUKOPLAKIA ORAL ( 12 FDA reports)
LHERMITTE'S SIGN ( 12 FDA reports)
LYMPHADENECTOMY ( 12 FDA reports)
NEPHROSCLEROSIS ( 12 FDA reports)
NODAL OSTEOARTHRITIS ( 12 FDA reports)
OPEN WOUND ( 12 FDA reports)
PELVI-URETERIC OBSTRUCTION ( 12 FDA reports)
PERITONITIS ( 12 FDA reports)
PURULENT DISCHARGE ( 12 FDA reports)
SEPSIS SYNDROME ( 12 FDA reports)
SINUS BRADYCARDIA ( 12 FDA reports)
SINUS CONGESTION ( 12 FDA reports)
SPUTUM DISCOLOURED ( 12 FDA reports)
STAPHYLOCOCCAL SEPSIS ( 12 FDA reports)
SUICIDAL IDEATION ( 12 FDA reports)
TANDEM GAIT TEST ABNORMAL ( 12 FDA reports)
TUMOUR INVASION ( 12 FDA reports)
TUMOUR LYSIS SYNDROME ( 12 FDA reports)
UPPER RESPIRATORY TRACT CONGESTION ( 12 FDA reports)
URINARY TRACT INFECTION ENTEROCOCCAL ( 12 FDA reports)
VAGINAL HAEMORRHAGE ( 12 FDA reports)
VASOGENIC CEREBRAL OEDEMA ( 12 FDA reports)
VISUAL IMPAIRMENT ( 12 FDA reports)
WALKING AID USER ( 12 FDA reports)
ABSCESS JAW ( 11 FDA reports)
ACIDOSIS ( 11 FDA reports)
ALVEOLITIS ( 11 FDA reports)
BONE EROSION ( 11 FDA reports)
BONE FORMATION INCREASED ( 11 FDA reports)
CALCINOSIS ( 11 FDA reports)
CATHETER PLACEMENT ( 11 FDA reports)
CERVICAL DYSPLASIA ( 11 FDA reports)
CERVICITIS HUMAN PAPILLOMA VIRUS ( 11 FDA reports)
DEVICE RELATED SEPSIS ( 11 FDA reports)
DRUG INTOLERANCE ( 11 FDA reports)
DRUG TOXICITY ( 11 FDA reports)
DYSLIPIDAEMIA ( 11 FDA reports)
ELECTROCARDIOGRAM QT PROLONGED ( 11 FDA reports)
ENCEPHALOPATHY ( 11 FDA reports)
ERECTILE DYSFUNCTION ( 11 FDA reports)
ERYTHEMA OF EYELID ( 11 FDA reports)
EYE HAEMORRHAGE ( 11 FDA reports)
EYELID OEDEMA ( 11 FDA reports)
GASTROENTERITIS ( 11 FDA reports)
GASTROINTESTINAL PERFORATION ( 11 FDA reports)
HEPATIC NEOPLASM ( 11 FDA reports)
HEPATIC STEATOSIS ( 11 FDA reports)
HILAR LYMPHADENOPATHY ( 11 FDA reports)
INGUINAL MASS ( 11 FDA reports)
INJECTION SITE PHLEBITIS ( 11 FDA reports)
IRRITABLE BOWEL SYNDROME ( 11 FDA reports)
MALIGNANT MELANOMA ( 11 FDA reports)
METASTASES TO MENINGES ( 11 FDA reports)
MYOCLONUS ( 11 FDA reports)
ORAL DISCOMFORT ( 11 FDA reports)
OSTEITIS ( 11 FDA reports)
PEPTIC ULCER ( 11 FDA reports)
PERIODONTAL INFECTION ( 11 FDA reports)
PNEUMONIA BACTERIAL ( 11 FDA reports)
RALES ( 11 FDA reports)
RASH PUSTULAR ( 11 FDA reports)
SARCOIDOSIS ( 11 FDA reports)
SKIN FISSURES ( 11 FDA reports)
SPINAL X-RAY ABNORMAL ( 11 FDA reports)
SUPRAVENTRICULAR EXTRASYSTOLES ( 11 FDA reports)
SWOLLEN TONGUE ( 11 FDA reports)
SYNOVIAL CYST ( 11 FDA reports)
THYROID NEOPLASM ( 11 FDA reports)
TORTICOLLIS ( 11 FDA reports)
URINARY RETENTION ( 11 FDA reports)
VARICOSE VEIN ( 11 FDA reports)
VENTRICULAR FIBRILLATION ( 11 FDA reports)
VENTRICULAR HYPERTROPHY ( 11 FDA reports)
ABDOMINAL HERNIA ( 10 FDA reports)
ABDOMINAL NEOPLASM ( 10 FDA reports)
ACUTE MYOCARDIAL INFARCTION ( 10 FDA reports)
ACUTE PRERENAL FAILURE ( 10 FDA reports)
ACUTE RESPIRATORY DISTRESS SYNDROME ( 10 FDA reports)
AGITATION ( 10 FDA reports)
AGRANULOCYTOSIS ( 10 FDA reports)
ALANINE AMINOTRANSFERASE DECREASED ( 10 FDA reports)
AORTIC DISSECTION ( 10 FDA reports)
APHONIA ( 10 FDA reports)
ARRHYTHMIA ( 10 FDA reports)
AZOTAEMIA ( 10 FDA reports)
B-CELL LYMPHOMA RECURRENT ( 10 FDA reports)
BLOOD ALKALINE PHOSPHATASE DECREASED ( 10 FDA reports)
BLOOD TRIGLYCERIDES INCREASED ( 10 FDA reports)
BONE LOSS ( 10 FDA reports)
BOWEL MOVEMENT IRREGULARITY ( 10 FDA reports)
BRAIN NEOPLASM MALIGNANT ( 10 FDA reports)
BREAST NEOPLASM ( 10 FDA reports)
BURNING SENSATION ( 10 FDA reports)
CAROTID ARTERIAL EMBOLUS ( 10 FDA reports)
CAROTID ARTERY STENOSIS ( 10 FDA reports)
CENTRAL OBESITY ( 10 FDA reports)
COGNITIVE DISORDER ( 10 FDA reports)
CRANIAL NERVE DISORDER ( 10 FDA reports)
CYST ASPIRATION ( 10 FDA reports)
EMOTIONAL DISORDER ( 10 FDA reports)
ENCEPHALITIS HERPES ( 10 FDA reports)
EPIDERMAL GROWTH FACTOR RECEPTOR INCREASED ( 10 FDA reports)
EROSIVE OESOPHAGITIS ( 10 FDA reports)
ERUCTATION ( 10 FDA reports)
EXCESSIVE GRANULATION TISSUE ( 10 FDA reports)
FEMORAL NECK FRACTURE ( 10 FDA reports)
GINGIVAL SWELLING ( 10 FDA reports)
HAEMODIALYSIS ( 10 FDA reports)
HEPATIC CYST ( 10 FDA reports)
HYDROCEPHALUS ( 10 FDA reports)
HYPOACUSIS ( 10 FDA reports)
INCONTINENCE ( 10 FDA reports)
INFUSION SITE ERYTHEMA ( 10 FDA reports)
INTESTINAL OBSTRUCTION ( 10 FDA reports)
IRRITABILITY ( 10 FDA reports)
JOINT SPRAIN ( 10 FDA reports)
JOINT STIFFNESS ( 10 FDA reports)
LACTIC ACIDOSIS ( 10 FDA reports)
LIP PAIN ( 10 FDA reports)
MEDICATION ERROR ( 10 FDA reports)
MENOPAUSE ( 10 FDA reports)
METASTASES TO LYMPH NODES ( 10 FDA reports)
METASTASES TO THE MEDIASTINUM ( 10 FDA reports)
MICROCYTOSIS ( 10 FDA reports)
MULTIPLE MYELOMA ( 10 FDA reports)
NEUTROPENIC SEPSIS ( 10 FDA reports)
ORAL MUCOSAL EXFOLIATION ( 10 FDA reports)
PAPILLOEDEMA ( 10 FDA reports)
PELVIC PAIN ( 10 FDA reports)
PERIODONTAL OPERATION ( 10 FDA reports)
PLEURAL FIBROSIS ( 10 FDA reports)
PNEUMOTHORAX ( 10 FDA reports)
RADICULAR SYNDROME ( 10 FDA reports)
RESPIRATORY TRACT CONGESTION ( 10 FDA reports)
RESTLESSNESS ( 10 FDA reports)
SALIVARY GLAND DISORDER ( 10 FDA reports)
SEASONAL ALLERGY ( 10 FDA reports)
SENSATION OF HEAVINESS ( 10 FDA reports)
SKIN FRAGILITY ( 10 FDA reports)
SMALL INTESTINAL OBSTRUCTION ( 10 FDA reports)
TELANGIECTASIA ( 10 FDA reports)
THORACIC VERTEBRAL FRACTURE ( 10 FDA reports)
VULVOVAGINAL DRYNESS ( 10 FDA reports)
WISDOM TEETH REMOVAL ( 10 FDA reports)
X-RAY ( 10 FDA reports)
ABDOMINAL MASS ( 9 FDA reports)
BACTERIAL TEST POSITIVE ( 9 FDA reports)
BARRETT'S OESOPHAGUS ( 9 FDA reports)
BIOPSY BONE ( 9 FDA reports)
BLOOD BILIRUBIN INCREASED ( 9 FDA reports)
BODY HEIGHT DECREASED ( 9 FDA reports)
BONE DEVELOPMENT ABNORMAL ( 9 FDA reports)
BONE MARROW DISORDER ( 9 FDA reports)
BONE MARROW OEDEMA ( 9 FDA reports)
BREAST DISCHARGE ( 9 FDA reports)
BUNDLE BRANCH BLOCK RIGHT ( 9 FDA reports)
CEREBRAL ISCHAEMIA ( 9 FDA reports)
CHEILITIS ( 9 FDA reports)
CONGENITAL CYSTIC KIDNEY DISEASE ( 9 FDA reports)
DEMYELINATING POLYNEUROPATHY ( 9 FDA reports)
DENTAL CARE ( 9 FDA reports)
DISORIENTATION ( 9 FDA reports)
DIVERTICULITIS ( 9 FDA reports)
EYE DISCHARGE ( 9 FDA reports)
EYE PAIN ( 9 FDA reports)
EYELID PTOSIS ( 9 FDA reports)
FLUID OVERLOAD ( 9 FDA reports)
FOREIGN BODY ( 9 FDA reports)
GASTRITIS EROSIVE ( 9 FDA reports)
HAEMATEMESIS ( 9 FDA reports)
HYPERAMMONAEMIA ( 9 FDA reports)
HYPERBARIC OXYGEN THERAPY ( 9 FDA reports)
HYPERMETABOLISM ( 9 FDA reports)
HYPERPARATHYROIDISM ( 9 FDA reports)
HYPERPHOSPHATAEMIA ( 9 FDA reports)
HYPOTHYROIDISM ( 9 FDA reports)
INAPPROPRIATE ANTIDIURETIC HORMONE SECRETION ( 9 FDA reports)
INJECTION SITE INDURATION ( 9 FDA reports)
INTERVERTEBRAL DISC COMPRESSION ( 9 FDA reports)
LACUNAR INFARCTION ( 9 FDA reports)
LIVER FUNCTION TEST ABNORMAL ( 9 FDA reports)
LUNG NEOPLASM MALIGNANT ( 9 FDA reports)
MACROCYTOSIS ( 9 FDA reports)
MACROGLOSSIA ( 9 FDA reports)
MEDIASTINAL DISORDER ( 9 FDA reports)
METABOLIC DISORDER ( 9 FDA reports)
MUCOSAL EROSION ( 9 FDA reports)
NASAL MUCOSAL DISORDER ( 9 FDA reports)
NEUROGENIC BLADDER ( 9 FDA reports)
NORMOCHROMIC NORMOCYTIC ANAEMIA ( 9 FDA reports)
OCCULT BLOOD POSITIVE ( 9 FDA reports)
OFF LABEL USE ( 9 FDA reports)
PANCREATITIS ACUTE ( 9 FDA reports)
PELVIC FRACTURE ( 9 FDA reports)
PERIARTHRITIS ( 9 FDA reports)
PERICARDIAL CYST ( 9 FDA reports)
PHOTOPSIA ( 9 FDA reports)
PROSTHESIS IMPLANTATION ( 9 FDA reports)
PULSE ABSENT ( 9 FDA reports)
RASH PRURITIC ( 9 FDA reports)
RENAL CANCER ( 9 FDA reports)
RESPIRATORY RATE INCREASED ( 9 FDA reports)
RHINITIS ( 9 FDA reports)
ROAD TRAFFIC ACCIDENT ( 9 FDA reports)
SCIATICA ( 9 FDA reports)
SERUM FERRITIN INCREASED ( 9 FDA reports)
SHOULDER DEFORMITY ( 9 FDA reports)
SKIN BURNING SENSATION ( 9 FDA reports)
SKIN OEDEMA ( 9 FDA reports)
SPINAL FRACTURE ( 9 FDA reports)
TEMPOROMANDIBULAR JOINT SYNDROME ( 9 FDA reports)
THYROID ADENOMA ( 9 FDA reports)
THYROID CYST ( 9 FDA reports)
TINNITUS ( 9 FDA reports)
TONGUE PARALYSIS ( 9 FDA reports)
TOOTH RESORPTION ( 9 FDA reports)
VIRAL INFECTION ( 9 FDA reports)
AFFECTIVE DISORDER ( 8 FDA reports)
AMENORRHOEA ( 8 FDA reports)
AORTIC STENOSIS ( 8 FDA reports)
AORTIC THROMBOSIS ( 8 FDA reports)
ASBESTOSIS ( 8 FDA reports)
BACTERIAL SEPSIS ( 8 FDA reports)
BIOPSY BONE MARROW ( 8 FDA reports)
BLISTER ( 8 FDA reports)
BLOOD IMMUNOGLOBULIN A INCREASED ( 8 FDA reports)
BLOOD PRESSURE SYSTOLIC INCREASED ( 8 FDA reports)
BONE FISTULA ( 8 FDA reports)
BREAST CANCER RECURRENT ( 8 FDA reports)
BREAST PAIN ( 8 FDA reports)
BREAST PROSTHESIS IMPLANTATION ( 8 FDA reports)
BREAST SWELLING ( 8 FDA reports)
BREAST TENDERNESS ( 8 FDA reports)
BREATH SOUNDS ABNORMAL ( 8 FDA reports)
BRONCHOSPASM ( 8 FDA reports)
CARCINOEMBRYONIC ANTIGEN INCREASED ( 8 FDA reports)
CATARACT OPERATION ( 8 FDA reports)
COLD SWEAT ( 8 FDA reports)
COLONOSCOPY ABNORMAL ( 8 FDA reports)
CONJUNCTIVITIS INFECTIVE ( 8 FDA reports)
CYANOSIS ( 8 FDA reports)
DIASTOLIC DYSFUNCTION ( 8 FDA reports)
DRUG DEPENDENCE ( 8 FDA reports)
DRY MOUTH ( 8 FDA reports)
EAR HAEMORRHAGE ( 8 FDA reports)
FOOT FRACTURE ( 8 FDA reports)
GASTROINTESTINAL SOUNDS ABNORMAL ( 8 FDA reports)
GYNAECOMASTIA ( 8 FDA reports)
HEPATIC FUNCTION ABNORMAL ( 8 FDA reports)
HEPATITIS C ( 8 FDA reports)
HYPERNATRAEMIA ( 8 FDA reports)
INFUSION SITE SWELLING ( 8 FDA reports)
INJECTION SITE EXTRAVASATION ( 8 FDA reports)
INJECTION SITE REACTION ( 8 FDA reports)
INTERNATIONAL NORMALISED RATIO INCREASED ( 8 FDA reports)
JAW OPERATION ( 8 FDA reports)
LEFT VENTRICULAR DYSFUNCTION ( 8 FDA reports)
LUMBAR RADICULOPATHY ( 8 FDA reports)
MASTICATION DISORDER ( 8 FDA reports)
MEDICAL DEVICE COMPLICATION ( 8 FDA reports)
METABOLIC ALKALOSIS ( 8 FDA reports)
METASTASES TO SKIN ( 8 FDA reports)
MUSCULOSKELETAL DISORDER ( 8 FDA reports)
NEPHROTIC SYNDROME ( 8 FDA reports)
NO ADVERSE EVENT ( 8 FDA reports)
RADICULITIS ( 8 FDA reports)
RED BLOOD CELL SCHISTOCYTES PRESENT ( 8 FDA reports)
RENAL PAIN ( 8 FDA reports)
SINGLE FUNCTIONAL KIDNEY ( 8 FDA reports)
STAPHYLOCOCCAL INFECTION ( 8 FDA reports)
STENT PLACEMENT ( 8 FDA reports)
THROAT IRRITATION ( 8 FDA reports)
TONGUE NEOPLASM ( 8 FDA reports)
TOTAL LUNG CAPACITY DECREASED ( 8 FDA reports)
TYPE 2 DIABETES MELLITUS ( 8 FDA reports)
URINE ANALYSIS ABNORMAL ( 8 FDA reports)
VENOUS STENOSIS ( 8 FDA reports)
VERTEBRAL COLUMN MASS ( 8 FDA reports)
VIRAL UPPER RESPIRATORY TRACT INFECTION ( 8 FDA reports)
VOCAL CORD PARALYSIS ( 8 FDA reports)
BILIARY COLIC ( 7 FDA reports)
BLOOD ALBUMIN DECREASED ( 7 FDA reports)
BLOOD CHLORIDE INCREASED ( 7 FDA reports)
BODY TEMPERATURE INCREASED ( 7 FDA reports)
BONE OPERATION ( 7 FDA reports)
C-REACTIVE PROTEIN INCREASED ( 7 FDA reports)
CALCIFICATION METASTATIC ( 7 FDA reports)
CARDIOTOXICITY ( 7 FDA reports)
CEREBRAL HAEMORRHAGE ( 7 FDA reports)
CEREBROVASCULAR DISORDER ( 7 FDA reports)
CERUMEN IMPACTION ( 7 FDA reports)
CHLOASMA ( 7 FDA reports)
CIRCULATORY COLLAPSE ( 7 FDA reports)
COLITIS ISCHAEMIC ( 7 FDA reports)
COLON CANCER METASTATIC ( 7 FDA reports)
CYST REMOVAL ( 7 FDA reports)
DEAFNESS NEUROSENSORY ( 7 FDA reports)
DIVERTICULUM INTESTINAL ( 7 FDA reports)
EMPHYSEMA ( 7 FDA reports)
ENDOTRACHEAL INTUBATION ( 7 FDA reports)
FAILURE TO THRIVE ( 7 FDA reports)
FAT NECROSIS ( 7 FDA reports)
FOLATE DEFICIENCY ( 7 FDA reports)
FOOD POISONING ( 7 FDA reports)
GASTRIC ULCER ( 7 FDA reports)
GASTROINTESTINAL NECROSIS ( 7 FDA reports)
GINGIVAL ABSCESS ( 7 FDA reports)
GRAND MAL CONVULSION ( 7 FDA reports)
HAEMOLYSIS ( 7 FDA reports)
HAEMORRHOIDAL HAEMORRHAGE ( 7 FDA reports)
HEPATIC ENZYME INCREASED ( 7 FDA reports)
HEPATOSPLENOMEGALY ( 7 FDA reports)
HYPERHOMOCYSTEINAEMIA ( 7 FDA reports)
INJECTION SITE ERYTHEMA ( 7 FDA reports)
INTERCOSTAL NEURALGIA ( 7 FDA reports)
LOWER LIMB FRACTURE ( 7 FDA reports)
MELANOCYTIC NAEVUS ( 7 FDA reports)
METABOLIC ENCEPHALOPATHY ( 7 FDA reports)
MUCOSAL ULCERATION ( 7 FDA reports)
NASAL CONGESTION ( 7 FDA reports)
NERVOUS SYSTEM DISORDER ( 7 FDA reports)
ONYCHOMYCOSIS ( 7 FDA reports)
ORAL SURGERY ( 7 FDA reports)
PERIVASCULAR DERMATITIS ( 7 FDA reports)
PHARYNGEAL OEDEMA ( 7 FDA reports)
PHOTOSENSITIVITY REACTION ( 7 FDA reports)
POLYDIPSIA ( 7 FDA reports)
PTERYGIUM ( 7 FDA reports)
RED MAN SYNDROME ( 7 FDA reports)
REFLUX LARYNGITIS ( 7 FDA reports)
RESPIRATORY DISORDER ( 7 FDA reports)
RIGHT ATRIAL DILATATION ( 7 FDA reports)
ROTATOR CUFF REPAIR ( 7 FDA reports)
SKIN HYPERPIGMENTATION ( 7 FDA reports)
SKIN PAPILLOMA ( 7 FDA reports)
SQUAMOUS CELL CARCINOMA ( 7 FDA reports)
STRESS FRACTURE ( 7 FDA reports)
SUBCUTANEOUS HAEMATOMA ( 7 FDA reports)
THERAPY NON-RESPONDER ( 7 FDA reports)
TOXIC EPIDERMAL NECROLYSIS ( 7 FDA reports)
ULCER ( 7 FDA reports)
VENTRICULAR TACHYCARDIA ( 7 FDA reports)
VISUAL ACUITY REDUCED ( 7 FDA reports)
VITREOUS FLOATERS ( 7 FDA reports)
ABASIA ( 6 FDA reports)
ABDOMINAL DISCOMFORT ( 6 FDA reports)
ADVERSE EVENT ( 6 FDA reports)
ANAPHYLACTOID REACTION ( 6 FDA reports)
ARTHRITIS ( 6 FDA reports)
BLOOD CREATINE PHOSPHOKINASE INCREASED ( 6 FDA reports)
BLOOD ELECTROLYTES ABNORMAL ( 6 FDA reports)
BLOOD ERYTHROPOIETIN INCREASED ( 6 FDA reports)
BLOOD PRESSURE IMMEASURABLE ( 6 FDA reports)
BLOOD URIC ACID INCREASED ( 6 FDA reports)
BONE CYST ( 6 FDA reports)
BONE MARROW TRANSPLANT ( 6 FDA reports)
CACHEXIA ( 6 FDA reports)
CHAPPED LIPS ( 6 FDA reports)
COMA ( 6 FDA reports)
DEAFNESS ( 6 FDA reports)
DERMOID CYST ( 6 FDA reports)
DIABETES MELLITUS ( 6 FDA reports)
DYSCHEZIA ( 6 FDA reports)
ENTEROCOCCAL INFECTION ( 6 FDA reports)
EPHELIDES ( 6 FDA reports)
ERYTHEMA MULTIFORME ( 6 FDA reports)
FOOT DEFORMITY ( 6 FDA reports)
GALLBLADDER DISORDER ( 6 FDA reports)
GASTRIC DISORDER ( 6 FDA reports)
GASTRITIS ( 6 FDA reports)
GRIMACING ( 6 FDA reports)
HAEMORRHAGE URINARY TRACT ( 6 FDA reports)
HALLUCINATION ( 6 FDA reports)
HEPATIC CIRRHOSIS ( 6 FDA reports)
HODGKIN'S DISEASE STAGE IV ( 6 FDA reports)
HOMOCYSTINAEMIA ( 6 FDA reports)
INFUSION SITE PAIN ( 6 FDA reports)
INGUINAL HERNIA ( 6 FDA reports)
LEUKOENCEPHALOPATHY ( 6 FDA reports)
LIPODYSTROPHY ACQUIRED ( 6 FDA reports)
LIPOMA ( 6 FDA reports)
LYMPHATIC OBSTRUCTION ( 6 FDA reports)
MAMMOPLASTY ( 6 FDA reports)
MASS EXCISION ( 6 FDA reports)
MEAN CELL VOLUME INCREASED ( 6 FDA reports)
MEDICAL DEVICE REMOVAL ( 6 FDA reports)
METASTASES TO PELVIS ( 6 FDA reports)
METASTASIS ( 6 FDA reports)
MICTURITION URGENCY ( 6 FDA reports)
NASAL ULCER ( 6 FDA reports)
NEUROPATHY ( 6 FDA reports)
NON-CARDIAC CHEST PAIN ( 6 FDA reports)
ORAL CAVITY FISTULA ( 6 FDA reports)
OXYGEN SUPPLEMENTATION ( 6 FDA reports)
PARTNER STRESS ( 6 FDA reports)
PERICARDIAL EFFUSION ( 6 FDA reports)
PERICARDITIS ( 6 FDA reports)
PNEUMATOSIS INTESTINALIS ( 6 FDA reports)
POLYNEUROPATHY ( 6 FDA reports)
POLYURIA ( 6 FDA reports)
POOR DENTAL CONDITION ( 6 FDA reports)
PROSTATITIS ( 6 FDA reports)
PROSTATOMEGALY ( 6 FDA reports)
PULMONARY CONGESTION ( 6 FDA reports)
PULMONARY OEDEMA ( 6 FDA reports)
PULMONARY THROMBOSIS ( 6 FDA reports)
RASH MACULAR ( 6 FDA reports)
RENAL DISORDER ( 6 FDA reports)
RESIDUAL URINE VOLUME ( 6 FDA reports)
RESPIRATORY RATE DECREASED ( 6 FDA reports)
SACRALISATION ( 6 FDA reports)
SINUS POLYP ( 6 FDA reports)
SPONDYLOLISTHESIS ( 6 FDA reports)
SUTURE RELATED COMPLICATION ( 6 FDA reports)
TENOSYNOVITIS ( 6 FDA reports)
TESTICULAR MASS ( 6 FDA reports)
TOXICITY TO VARIOUS AGENTS ( 6 FDA reports)
URETHRAL STENOSIS ( 6 FDA reports)
URETHRITIS ( 6 FDA reports)
URINE OUTPUT DECREASED ( 6 FDA reports)
VERTEBRAL FORAMINAL STENOSIS ( 6 FDA reports)
VERTIGO ( 6 FDA reports)
VITAMIN B12 INCREASED ( 6 FDA reports)
VOMITING PROJECTILE ( 6 FDA reports)
ANTIBIOTIC RESISTANT STAPHYLOCOCCUS TEST POSITIVE ( 5 FDA reports)
APHTHOUS STOMATITIS ( 5 FDA reports)
APPENDICECTOMY ( 5 FDA reports)
ATRIAL FLUTTER ( 5 FDA reports)
BLEPHARITIS ( 5 FDA reports)
BLOOD AMYLASE INCREASED ( 5 FDA reports)
BLOOD CREATINE PHOSPHOKINASE MB INCREASED ( 5 FDA reports)
BLOOD GLUCOSE DECREASED ( 5 FDA reports)
BRAIN MASS ( 5 FDA reports)
BREAST CANCER IN SITU ( 5 FDA reports)
CATHETER SITE HAEMORRHAGE ( 5 FDA reports)
CEREBROSPINAL FLUID RESERVOIR PLACEMENT ( 5 FDA reports)
CHOLECYSTITIS ( 5 FDA reports)
CLOSED FRACTURE MANIPULATION ( 5 FDA reports)
CORONARY ARTERY STENOSIS ( 5 FDA reports)
DERMATITIS ( 5 FDA reports)
DUODENAL ULCER ( 5 FDA reports)
DUODENAL ULCER PERFORATION ( 5 FDA reports)
EATING DISORDER ( 5 FDA reports)
ENTEROCOCCAL BACTERAEMIA ( 5 FDA reports)
FACE OEDEMA ( 5 FDA reports)
GASTROINTESTINAL DISORDER ( 5 FDA reports)
GASTROINTESTINAL MOTILITY DISORDER ( 5 FDA reports)
HAEMOLYTIC ANAEMIA ( 5 FDA reports)
HAEMOLYTIC URAEMIC SYNDROME ( 5 FDA reports)
HALLUCINATION, VISUAL ( 5 FDA reports)
HEPATIC ENCEPHALOPATHY ( 5 FDA reports)
HEPATIC HAEMORRHAGE ( 5 FDA reports)
HOT FLUSH ( 5 FDA reports)
HYPERTENSIVE ANGIOPATHY ( 5 FDA reports)
HYPOAESTHESIA FACIAL ( 5 FDA reports)
INFECTED SEBACEOUS CYST ( 5 FDA reports)
INFECTIOUS PERITONITIS ( 5 FDA reports)
INFLUENZA ( 5 FDA reports)
INFUSION SITE PHLEBITIS ( 5 FDA reports)
LARGE INTESTINE PERFORATION ( 5 FDA reports)
LESION EXCISION ( 5 FDA reports)
LIGAMENT INJURY ( 5 FDA reports)
LIPASE INCREASED ( 5 FDA reports)
LYMPHOPENIA ( 5 FDA reports)
MEMORY IMPAIRMENT ( 5 FDA reports)
METASTASES TO PERITONEUM ( 5 FDA reports)
MUSCLE TIGHTNESS ( 5 FDA reports)
MUSCULOSKELETAL DISCOMFORT ( 5 FDA reports)
NECROSIS ( 5 FDA reports)
NERVE ROOT COMPRESSION ( 5 FDA reports)
ORAL FUNGAL INFECTION ( 5 FDA reports)
ORAL SOFT TISSUE DISORDER ( 5 FDA reports)
ORAL SUBMUCOSAL FIBROSIS ( 5 FDA reports)
PARALYSIS FLACCID ( 5 FDA reports)
PHARYNGITIS ( 5 FDA reports)
PHARYNGOLARYNGEAL PAIN ( 5 FDA reports)
PHLEBITIS ( 5 FDA reports)
PLATELET COUNT INCREASED ( 5 FDA reports)
PROSTATE CANCER METASTATIC ( 5 FDA reports)
PULMONARY HYPERTENSION ( 5 FDA reports)
PUPILS UNEQUAL ( 5 FDA reports)
RED CELL DISTRIBUTION WIDTH INCREASED ( 5 FDA reports)
RHABDOMYOLYSIS ( 5 FDA reports)
SHOCK ( 5 FDA reports)
SKIN CHAPPED ( 5 FDA reports)
SMALL INTESTINAL HAEMORRHAGE ( 5 FDA reports)
SPONDYLOLYSIS ( 5 FDA reports)
THROMBOSIS ( 5 FDA reports)
TRACHEO-OESOPHAGEAL FISTULA ( 5 FDA reports)
UNDERDOSE ( 5 FDA reports)
UROSEPSIS ( 5 FDA reports)
UTERINE LEIOMYOMA ( 5 FDA reports)
VENTRICULAR EXTRASYSTOLES ( 5 FDA reports)
VISUAL DISTURBANCE ( 5 FDA reports)
ABDOMINAL INFECTION ( 4 FDA reports)
ACUTE HEPATIC FAILURE ( 4 FDA reports)
ACUTE MYELOID LEUKAEMIA ( 4 FDA reports)
ACUTE MYELOMONOCYTIC LEUKAEMIA ( 4 FDA reports)
AORTIC DISORDER ( 4 FDA reports)
ARTERIOSCLEROSIS CORONARY ARTERY ( 4 FDA reports)
BACTERIAL INFECTION ( 4 FDA reports)
BIPOLAR DISORDER ( 4 FDA reports)
BLINDNESS ( 4 FDA reports)
BLOOD CHLORIDE DECREASED ( 4 FDA reports)
BLOOD OESTROGEN INCREASED ( 4 FDA reports)
BLOOD PRESSURE DIASTOLIC DECREASED ( 4 FDA reports)
BODY TEMPERATURE DECREASED ( 4 FDA reports)
BODY TINEA ( 4 FDA reports)
BONE LESION EXCISION ( 4 FDA reports)
BRADYKINESIA ( 4 FDA reports)
BRONCHOPNEUMONIA ( 4 FDA reports)
BUTTOCK PAIN ( 4 FDA reports)
CANCER PAIN ( 4 FDA reports)
CARDIOVASCULAR DISORDER ( 4 FDA reports)
CAROTID BRUIT ( 4 FDA reports)
CATHETER SITE PAIN ( 4 FDA reports)
CLOSTRIDIAL INFECTION ( 4 FDA reports)
COLON CANCER ( 4 FDA reports)
DELIRIUM ( 4 FDA reports)
DISEASE RECURRENCE ( 4 FDA reports)
DUODENITIS ( 4 FDA reports)
DYSKINESIA ( 4 FDA reports)
ELECTROCARDIOGRAM ST SEGMENT DEPRESSION ( 4 FDA reports)
EMBOLIC STROKE ( 4 FDA reports)
FACIAL BONES FRACTURE ( 4 FDA reports)
FACIAL PAIN ( 4 FDA reports)
FEELING COLD ( 4 FDA reports)
FUNGAEMIA ( 4 FDA reports)
GINGIVAL DISORDER ( 4 FDA reports)
GINGIVAL RECESSION ( 4 FDA reports)
GROIN PAIN ( 4 FDA reports)
HEPATIC NECROSIS ( 4 FDA reports)
HICCUPS ( 4 FDA reports)
HYPERURICAEMIA ( 4 FDA reports)
HYPOALBUMINAEMIA ( 4 FDA reports)
HYPOGAMMAGLOBULINAEMIA ( 4 FDA reports)
HYPOGLYCAEMIA ( 4 FDA reports)
INCORRECT DRUG ADMINISTRATION RATE ( 4 FDA reports)
INFARCTION ( 4 FDA reports)
INFUSION SITE REACTION ( 4 FDA reports)
INTERVERTEBRAL DISC DISORDER ( 4 FDA reports)
INTESTINAL FUNCTIONAL DISORDER ( 4 FDA reports)
JAW FRACTURE ( 4 FDA reports)
LACRIMATION INCREASED ( 4 FDA reports)
LARGE INTESTINAL HAEMORRHAGE ( 4 FDA reports)
LIMB DISCOMFORT ( 4 FDA reports)
LIP BLISTER ( 4 FDA reports)
LIP SWELLING ( 4 FDA reports)
LIVER DISORDER ( 4 FDA reports)
LUMBOSACRAL PLEXUS LESION ( 4 FDA reports)
LYMPHADENITIS ( 4 FDA reports)
MARKEDLY REDUCED DIETARY INTAKE ( 4 FDA reports)
MECHANICAL VENTILATION ( 4 FDA reports)
METABOLIC SYNDROME ( 4 FDA reports)
MODIFIED RADICAL MASTECTOMY ( 4 FDA reports)
MOUTH CYST ( 4 FDA reports)
MOVEMENT DISORDER ( 4 FDA reports)
MUSCLE ATROPHY ( 4 FDA reports)
MUSCLE RIGIDITY ( 4 FDA reports)
MUSCULOSKELETAL STIFFNESS ( 4 FDA reports)
MYELOMA RECURRENCE ( 4 FDA reports)
NARCOLEPSY ( 4 FDA reports)
NASAL DISCOMFORT ( 4 FDA reports)
NEURALGIA ( 4 FDA reports)
NO THERAPEUTIC RESPONSE ( 4 FDA reports)
OEDEMA MOUTH ( 4 FDA reports)
OSTEITIS DEFORMANS ( 4 FDA reports)
PAIN OF SKIN ( 4 FDA reports)
PANCREATIC CARCINOMA ( 4 FDA reports)
PARAPLEGIA ( 4 FDA reports)
PATELLA FRACTURE ( 4 FDA reports)
PHOTOPHOBIA ( 4 FDA reports)
PNEUMONIA FUNGAL ( 4 FDA reports)
PNEUMONIA VIRAL ( 4 FDA reports)
POST PROCEDURAL COMPLICATION ( 4 FDA reports)
PRESYNCOPE ( 4 FDA reports)
PROSTATIC SPECIFIC ANTIGEN INCREASED ( 4 FDA reports)
PROTEIN TOTAL INCREASED ( 4 FDA reports)
PROTEINURIA ( 4 FDA reports)
RADIATION INJURY ( 4 FDA reports)
RADIATION SKIN INJURY ( 4 FDA reports)
RHINITIS ALLERGIC ( 4 FDA reports)
RHINORRHOEA ( 4 FDA reports)
SCROTAL OEDEMA ( 4 FDA reports)
STRESS ( 4 FDA reports)
STRIDOR ( 4 FDA reports)
SYNCOPE VASOVAGAL ( 4 FDA reports)
TACHYPNOEA ( 4 FDA reports)
TENDERNESS ( 4 FDA reports)
TENDONITIS ( 4 FDA reports)
THROMBOPHLEBITIS SUPERFICIAL ( 4 FDA reports)
UNEVALUABLE EVENT ( 4 FDA reports)
VAGINAL DISCHARGE ( 4 FDA reports)
VAGINAL INFECTION ( 4 FDA reports)
WOUND DEBRIDEMENT ( 4 FDA reports)
WRONG TECHNIQUE IN DRUG USAGE PROCESS ( 4 FDA reports)
ACTIVATED PARTIAL THROMBOPLASTIN TIME PROLONGED ( 3 FDA reports)
ADENOMATOUS POLYPOSIS COLI ( 3 FDA reports)
ADRENAL INSUFFICIENCY ( 3 FDA reports)
ALPHA HAEMOLYTIC STREPTOCOCCAL INFECTION ( 3 FDA reports)
ANAL FISSURE ( 3 FDA reports)
APNOEA ( 3 FDA reports)
ATRIOVENTRICULAR BLOCK COMPLETE ( 3 FDA reports)
AXILLARY MASS ( 3 FDA reports)
BLAST CELL COUNT INCREASED ( 3 FDA reports)
BLEPHAROSPASM ( 3 FDA reports)
BLOOD CULTURE POSITIVE ( 3 FDA reports)
BLOOD PHOSPHORUS INCREASED ( 3 FDA reports)
CAMPYLOBACTER INFECTION ( 3 FDA reports)
CARDIAC DISORDER ( 3 FDA reports)
CAROTID ARTERY OCCLUSION ( 3 FDA reports)
CLONUS ( 3 FDA reports)
COELIAC DISEASE ( 3 FDA reports)
CONCUSSION ( 3 FDA reports)
CONDUCTION DISORDER ( 3 FDA reports)
COORDINATION ABNORMAL ( 3 FDA reports)
CRANIOTOMY ( 3 FDA reports)
CULTURE URINE POSITIVE ( 3 FDA reports)
DECUBITUS ULCER ( 3 FDA reports)
DIABETIC ENTEROPATHY ( 3 FDA reports)
DIABETIC ULCER ( 3 FDA reports)
DIVERTICULUM INTESTINAL HAEMORRHAGIC ( 3 FDA reports)
DRUG ADMINISTRATION ERROR ( 3 FDA reports)
DRUG INTERACTION ( 3 FDA reports)
DRY EYE ( 3 FDA reports)
DYSPNOEA AT REST ( 3 FDA reports)
ELECTROCARDIOGRAM QRS COMPLEX PROLONGED ( 3 FDA reports)
EMBOLIC CEREBRAL INFARCTION ( 3 FDA reports)
EMBOLISM ( 3 FDA reports)
ENCEPHALOMYELITIS ( 3 FDA reports)
EXTRANODAL MARGINAL ZONE B-CELL LYMPHOMA (MALT TYPE) ( 3 FDA reports)
EYE INFLAMMATION ( 3 FDA reports)
FACE INJURY ( 3 FDA reports)
FLUID INTAKE REDUCED ( 3 FDA reports)
FOAMING AT MOUTH ( 3 FDA reports)
GASTRIC MUCOSAL HYPERTROPHY ( 3 FDA reports)
GASTRIC VARICES HAEMORRHAGE ( 3 FDA reports)
GENERALISED ERYTHEMA ( 3 FDA reports)
GRANULOCYTOPENIA ( 3 FDA reports)
GRANULOMA ( 3 FDA reports)
GRAVITATIONAL OEDEMA ( 3 FDA reports)
HAEMORRHAGIC ANAEMIA ( 3 FDA reports)
HEPATITIS ACUTE ( 3 FDA reports)
HYDROPNEUMOTHORAX ( 3 FDA reports)
HYPERTENSIVE HEART DISEASE ( 3 FDA reports)
HYPOTONIA ( 3 FDA reports)
ILEAL PERFORATION ( 3 FDA reports)
INCREASED UPPER AIRWAY SECRETION ( 3 FDA reports)
INFUSION SITE OEDEMA ( 3 FDA reports)
INFUSION SITE URTICARIA ( 3 FDA reports)
INJECTION SITE BURNING ( 3 FDA reports)
INJECTION SITE NODULE ( 3 FDA reports)
JEJUNAL ULCER ( 3 FDA reports)
JUGULAR VEIN THROMBOSIS ( 3 FDA reports)
LACERATION ( 3 FDA reports)
LARYNGOSPASM ( 3 FDA reports)
LOWER GASTROINTESTINAL HAEMORRHAGE ( 3 FDA reports)
MALFORMATION VENOUS ( 3 FDA reports)
MALIGNANT PLEURAL EFFUSION ( 3 FDA reports)
MEAN CELL HAEMOGLOBIN INCREASED ( 3 FDA reports)
MIGRAINE ( 3 FDA reports)
MYOPATHY ( 3 FDA reports)
MYOSITIS ( 3 FDA reports)
NAIL DISORDER ( 3 FDA reports)
NERVE ROOT LESION ( 3 FDA reports)
NERVOUSNESS ( 3 FDA reports)
NEUTROPENIC INFECTION ( 3 FDA reports)
NON-HODGKIN'S LYMPHOMA ( 3 FDA reports)
NON-SMALL CELL LUNG CANCER ( 3 FDA reports)
OBESITY ( 3 FDA reports)
OCCIPITAL NEURALGIA ( 3 FDA reports)
OCULAR HYPERAEMIA ( 3 FDA reports)
OESOPHAGEAL ULCER ( 3 FDA reports)
ONYCHOCLASIS ( 3 FDA reports)
OPTIC NEURITIS ( 3 FDA reports)
OROPHARYNGEAL SWELLING ( 3 FDA reports)
PARALYSIS ( 3 FDA reports)
PHLEBITIS SUPERFICIAL ( 3 FDA reports)
PLEURAL DISORDER ( 3 FDA reports)
PNEUMONIA INFLUENZAL ( 3 FDA reports)
PNEUMONIA PRIMARY ATYPICAL ( 3 FDA reports)
POLYMYALGIA RHEUMATICA ( 3 FDA reports)
PORTAL VEIN PRESSURE INCREASED ( 3 FDA reports)
PORTAL VENOUS GAS ( 3 FDA reports)
PRESBYACUSIS ( 3 FDA reports)
PROCTALGIA ( 3 FDA reports)
PULMONARY TOXICITY ( 3 FDA reports)
PULSE PRESSURE DECREASED ( 3 FDA reports)
PURPURA ( 3 FDA reports)
PYELONEPHRITIS ( 3 FDA reports)
RADIATION NEUROPATHY ( 3 FDA reports)
RASH MACULO-PAPULAR ( 3 FDA reports)
RASH PAPULAR ( 3 FDA reports)
RECURRENT CANCER ( 3 FDA reports)
RESORPTION BONE INCREASED ( 3 FDA reports)
SENSATION OF PRESSURE ( 3 FDA reports)
SKIN INFECTION ( 3 FDA reports)
SKIN ODOUR ABNORMAL ( 3 FDA reports)
SMALL INTESTINAL PERFORATION ( 3 FDA reports)
SNEEZING ( 3 FDA reports)
SUBARACHNOID HAEMORRHAGE ( 3 FDA reports)
TEMPERATURE INTOLERANCE ( 3 FDA reports)
TEMPORAL ARTERITIS ( 3 FDA reports)
THYROID CANCER ( 3 FDA reports)
TRAUMATIC BRAIN INJURY ( 3 FDA reports)
TREATMENT NONCOMPLIANCE ( 3 FDA reports)
TRISMUS ( 3 FDA reports)
URINARY TRACT PAIN ( 3 FDA reports)
WHEELCHAIR USER ( 3 FDA reports)
ABDOMINAL PAIN LOWER ( 2 FDA reports)
ABORTION MISSED ( 2 FDA reports)
ABSCESS RUPTURE ( 2 FDA reports)
ACUTE LUNG INJURY ( 2 FDA reports)
ADVERSE DRUG REACTION ( 2 FDA reports)
ALLERGIC RESPIRATORY SYMPTOM ( 2 FDA reports)
ALTERED STATE OF CONSCIOUSNESS ( 2 FDA reports)
ALVEOLOPLASTY ( 2 FDA reports)
ANAEMIA OF CHRONIC DISEASE ( 2 FDA reports)
ANEURYSM ( 2 FDA reports)
ANOXIC ENCEPHALOPATHY ( 2 FDA reports)
ANXIETY DISORDER ( 2 FDA reports)
AORTIC ANEURYSM ( 2 FDA reports)
AORTIC ANEURYSM RUPTURE ( 2 FDA reports)
AORTIC DILATATION ( 2 FDA reports)
AORTIC VALVE STENOSIS ( 2 FDA reports)
ARTERIAL STENOSIS ( 2 FDA reports)
ARTERIOVENOUS FISTULA OPERATION ( 2 FDA reports)
ASEPTIC NECROSIS BONE ( 2 FDA reports)
ASPHYXIA ( 2 FDA reports)
ASPIRATION ( 2 FDA reports)
ASTHMA ( 2 FDA reports)
ATRIOVENTRICULAR BLOCK SECOND DEGREE ( 2 FDA reports)
AXILLARY PAIN ( 2 FDA reports)
BACTERIA URINE NO ORGANISM OBSERVED ( 2 FDA reports)
BILE DUCT CANCER ( 2 FDA reports)
BILIARY TRACT DISORDER ( 2 FDA reports)
BILIRUBIN CONJUGATED INCREASED ( 2 FDA reports)
BLADDER CANCER ( 2 FDA reports)
BLADDER MASS ( 2 FDA reports)
BLAST CELLS ( 2 FDA reports)
BLINDNESS UNILATERAL ( 2 FDA reports)
BLOOD ALBUMIN ABNORMAL ( 2 FDA reports)
BLOOD PH DECREASED ( 2 FDA reports)
BLOOD PHOSPHORUS DECREASED ( 2 FDA reports)
BLOOD PRESSURE ORTHOSTATIC ( 2 FDA reports)
BLOOD URINE PRESENT ( 2 FDA reports)
BONE SWELLING ( 2 FDA reports)
BRAIN NEOPLASM ( 2 FDA reports)
BREAST DISORDER ( 2 FDA reports)
BREATH ODOUR ( 2 FDA reports)
CARBON DIOXIDE DECREASED ( 2 FDA reports)
CARDIAC MURMUR FUNCTIONAL ( 2 FDA reports)
CARDIAC TAMPONADE ( 2 FDA reports)
CARDIAC VALVE DISEASE ( 2 FDA reports)
CARDIOACTIVE DRUG LEVEL INCREASED ( 2 FDA reports)
CARDIOGENIC SHOCK ( 2 FDA reports)
CARDIOPULMONARY FAILURE ( 2 FDA reports)
CAROTID ENDARTERECTOMY ( 2 FDA reports)
CATHETER RELATED COMPLICATION ( 2 FDA reports)
CATHETER SEPSIS ( 2 FDA reports)
CATHETER SITE RELATED REACTION ( 2 FDA reports)
CEREBRAL ARTERY OCCLUSION ( 2 FDA reports)
CHEST X-RAY ABNORMAL ( 2 FDA reports)
CHOLECYSTITIS ACUTE ( 2 FDA reports)
CHONDROMALACIA ( 2 FDA reports)
CLONIC CONVULSION ( 2 FDA reports)
COLLAPSE OF LUNG ( 2 FDA reports)
COLONIC POLYP ( 2 FDA reports)
COMA HEPATIC ( 2 FDA reports)
COOMBS TEST POSITIVE ( 2 FDA reports)
CORONARY ARTERIAL STENT INSERTION ( 2 FDA reports)
CORONARY ARTERY OCCLUSION ( 2 FDA reports)
CYANOSIS CENTRAL ( 2 FDA reports)
CYTOMEGALOVIRUS COLITIS ( 2 FDA reports)
CYTOMEGALOVIRUS TEST POSITIVE ( 2 FDA reports)
DERMATITIS CONTACT ( 2 FDA reports)
DEVICE DISLOCATION ( 2 FDA reports)
DIABETIC KETOACIDOSIS ( 2 FDA reports)
DIFFUSE ALVEOLAR DAMAGE ( 2 FDA reports)
DILATATION ATRIAL ( 2 FDA reports)
DIPLOPIA ( 2 FDA reports)
DRUG ERUPTION ( 2 FDA reports)
DRUG EXPOSURE DURING PREGNANCY ( 2 FDA reports)
DYSSTASIA ( 2 FDA reports)
DYSTONIA ( 2 FDA reports)
ELECTROCARDIOGRAM QRS COMPLEX ABNORMAL ( 2 FDA reports)
ELECTROCARDIOGRAM ST SEGMENT ABNORMAL ( 2 FDA reports)
ELECTROCARDIOGRAM T WAVE INVERSION ( 2 FDA reports)
ELECTROLYTE IMBALANCE ( 2 FDA reports)
EMPYEMA ( 2 FDA reports)
ENTEROCOLITIS ( 2 FDA reports)
EOSINOPHIL COUNT INCREASED ( 2 FDA reports)
EPILEPSY ( 2 FDA reports)
ESCHERICHIA INFECTION ( 2 FDA reports)
EXCORIATION ( 2 FDA reports)
EYE MOVEMENT DISORDER ( 2 FDA reports)
EYE ROLLING ( 2 FDA reports)
FLATULENCE ( 2 FDA reports)
FOETAL EXPOSURE DURING PREGNANCY ( 2 FDA reports)
FOLLICULITIS ( 2 FDA reports)
GASTRIC HAEMORRHAGE ( 2 FDA reports)
GASTRIC MUCOSAL LESION ( 2 FDA reports)
GASTRIC ULCER HAEMORRHAGE ( 2 FDA reports)
GASTROINTESTINAL OEDEMA ( 2 FDA reports)
GASTROINTESTINAL STOMA COMPLICATION ( 2 FDA reports)
GASTROINTESTINAL TOXICITY ( 2 FDA reports)
GAZE PALSY ( 2 FDA reports)
GENERAL PHYSICAL CONDITION ABNORMAL ( 2 FDA reports)
GRAFT LOSS ( 2 FDA reports)
GRAFT VERSUS HOST DISEASE ( 2 FDA reports)
GUILLAIN-BARRE SYNDROME ( 2 FDA reports)
HAIR GROWTH ABNORMAL ( 2 FDA reports)
HELICOBACTER GASTRITIS ( 2 FDA reports)
HEPATIC PAIN ( 2 FDA reports)
HEPATITIS B ( 2 FDA reports)
HEPATITIS FULMINANT ( 2 FDA reports)
HIRSUTISM ( 2 FDA reports)
HOARSENESS ( 2 FDA reports)
HOSPICE CARE ( 2 FDA reports)
HOSPITALISATION ( 2 FDA reports)
HUMERUS FRACTURE ( 2 FDA reports)
HYPERBILIRUBINAEMIA ( 2 FDA reports)
HYPERSOMNIA ( 2 FDA reports)
HYPERTRANSAMINASAEMIA ( 2 FDA reports)
IATROGENIC INJURY ( 2 FDA reports)
IDIOPATHIC PULMONARY FIBROSIS ( 2 FDA reports)
IIIRD NERVE PARALYSIS ( 2 FDA reports)
ILL-DEFINED DISORDER ( 2 FDA reports)
IMPETIGO ( 2 FDA reports)
IMPLANT SITE REACTION ( 2 FDA reports)
INADEQUATE ANALGESIA ( 2 FDA reports)
INAPPROPRIATE SCHEDULE OF DRUG ADMINISTRATION ( 2 FDA reports)
INCORRECT DOSE ADMINISTERED ( 2 FDA reports)
INFECTED DERMAL CYST ( 2 FDA reports)
INFECTIOUS PLEURAL EFFUSION ( 2 FDA reports)
INFLUENZA LIKE ILLNESS ( 2 FDA reports)
INFUSION SITE DISCOMFORT ( 2 FDA reports)
INFUSION SITE EXTRAVASATION ( 2 FDA reports)
INGROWING NAIL ( 2 FDA reports)
INJECTION SITE IRRITATION ( 2 FDA reports)
INJECTION SITE SWELLING ( 2 FDA reports)
INJECTION SITE THROMBOSIS ( 2 FDA reports)
INTERNATIONAL NORMALISED RATIO DECREASED ( 2 FDA reports)
INTRACRANIAL ANEURYSM ( 2 FDA reports)
ISCHAEMIC CEREBRAL INFARCTION ( 2 FDA reports)
KLEBSIELLA TEST POSITIVE ( 2 FDA reports)
LABORATORY TEST ABNORMAL ( 2 FDA reports)
LARGE INTESTINAL ULCER ( 2 FDA reports)
LARYNGEAL OEDEMA ( 2 FDA reports)
LOSS OF CONTROL OF LEGS ( 2 FDA reports)
MALIGNANT ASCITES ( 2 FDA reports)
MATERNAL EXPOSURE DURING PREGNANCY ( 2 FDA reports)
MENTAL DISORDER ( 2 FDA reports)
MICTURITION DISORDER ( 2 FDA reports)
MOOD ALTERED ( 2 FDA reports)
MUSCLE INJURY ( 2 FDA reports)
MYELITIS ( 2 FDA reports)
MYELODYSPLASTIC SYNDROME TRANSFORMATION ( 2 FDA reports)
NASAL SEPTUM PERFORATION ( 2 FDA reports)
NEPHROGENIC ANAEMIA ( 2 FDA reports)
NEUROTOXICITY ( 2 FDA reports)
NEUTROPENIC COLITIS ( 2 FDA reports)
NO ADVERSE DRUG EFFECT ( 2 FDA reports)
ODYNOPHAGIA ( 2 FDA reports)
ORGAN FAILURE ( 2 FDA reports)
OROPHARYNGEAL PAIN ( 2 FDA reports)
OSTEOMYELITIS ACUTE ( 2 FDA reports)
OSTEOSARCOMA METASTATIC ( 2 FDA reports)
OTORRHOEA ( 2 FDA reports)
PANCREATIC ATROPHY ( 2 FDA reports)
PARATRACHEAL LYMPHADENOPATHY ( 2 FDA reports)
PCO2 DECREASED ( 2 FDA reports)
PERIORBITAL OEDEMA ( 2 FDA reports)
PERIPHERAL COLDNESS ( 2 FDA reports)
PERIPHERAL MOTOR NEUROPATHY ( 2 FDA reports)
PERIPHERAL SENSORY NEUROPATHY ( 2 FDA reports)
PERIPHERAL VASCULAR DISORDER ( 2 FDA reports)
PERITONITIS BACTERIAL ( 2 FDA reports)
PLEURISY ( 2 FDA reports)
PLEURITIC PAIN ( 2 FDA reports)
PNEUMOCYSTIS JIROVECI PNEUMONIA ( 2 FDA reports)
PNEUMONIA STREPTOCOCCAL ( 2 FDA reports)
POST PROCEDURAL HAEMORRHAGE ( 2 FDA reports)
PROCEDURAL COMPLICATION ( 2 FDA reports)
PRODUCT QUALITY ISSUE ( 2 FDA reports)
PROTEIN TOTAL DECREASED ( 2 FDA reports)
PRURITUS GENERALISED ( 2 FDA reports)
PULMONARY ARTERY THROMBOSIS ( 2 FDA reports)
PULSELESS ELECTRICAL ACTIVITY ( 2 FDA reports)
PURULENCE ( 2 FDA reports)
REFUSAL OF TREATMENT BY PATIENT ( 2 FDA reports)
RETINAL ARTERY THROMBOSIS ( 2 FDA reports)
RHEUMATOID ARTHRITIS ( 2 FDA reports)
SALIVARY HYPERSECRETION ( 2 FDA reports)
SIMPLE PARTIAL SEIZURES ( 2 FDA reports)
SINUSITIS FUNGAL ( 2 FDA reports)
SKELETAL INJURY ( 2 FDA reports)
SKIN INJURY ( 2 FDA reports)
SKIN LESION ( 2 FDA reports)
SKIN PLAQUE ( 2 FDA reports)
SKIN STRIAE ( 2 FDA reports)
SLEEP TALKING ( 2 FDA reports)
SOLILOQUY ( 2 FDA reports)
STAPHYLOCOCCUS TEST POSITIVE ( 2 FDA reports)
STEVENS-JOHNSON SYNDROME ( 2 FDA reports)
STOMACH DISCOMFORT ( 2 FDA reports)
STREPTOCOCCUS TEST POSITIVE ( 2 FDA reports)
SURGERY ( 2 FDA reports)
SYNOVIAL DISORDER ( 2 FDA reports)
TENDON DISORDER ( 2 FDA reports)
TENDON RUPTURE ( 2 FDA reports)
THERAPEUTIC AGENT TOXICITY ( 2 FDA reports)
THERAPEUTIC RESPONSE DECREASED ( 2 FDA reports)
THERAPEUTIC RESPONSE UNEXPECTED ( 2 FDA reports)
TINEA PEDIS ( 2 FDA reports)
TONGUE BITING ( 2 FDA reports)
TONGUE OEDEMA ( 2 FDA reports)
TONGUE PIGMENTATION ( 2 FDA reports)
TRAUMATIC INTRACRANIAL HAEMORRHAGE ( 2 FDA reports)
TREATMENT FAILURE ( 2 FDA reports)
TROPONIN INCREASED ( 2 FDA reports)
TUMOUR PERFORATION ( 2 FDA reports)
TYPE I HYPERSENSITIVITY ( 2 FDA reports)
URETERAL NECROSIS ( 2 FDA reports)
URETERAL STENT INSERTION ( 2 FDA reports)
URETERIC OBSTRUCTION ( 2 FDA reports)
URINARY TRACT INFECTION STAPHYLOCOCCAL ( 2 FDA reports)
UVEITIS ( 2 FDA reports)
VARICES OESOPHAGEAL ( 2 FDA reports)
VASCULAR RUPTURE ( 2 FDA reports)
VASOCONSTRICTION ( 2 FDA reports)
VEIN DISORDER ( 2 FDA reports)
VENOUS THROMBOSIS LIMB ( 2 FDA reports)
VULVECTOMY ( 2 FDA reports)
WRIST FRACTURE ( 2 FDA reports)
ABDOMINAL ABSCESS ( 1 FDA reports)
ABDOMINAL ADHESIONS ( 1 FDA reports)
ABDOMINAL RIGIDITY ( 1 FDA reports)
ABDOMINAL WALL ABSCESS ( 1 FDA reports)
ACCOMMODATION DISORDER ( 1 FDA reports)
ACUTE GENERALISED EXANTHEMATOUS PUSTULOSIS ( 1 FDA reports)
ACUTE PULMONARY OEDEMA ( 1 FDA reports)
ACUTE SINUSITIS ( 1 FDA reports)
ADMINISTRATION SITE PAIN ( 1 FDA reports)
ADVERSE REACTION ( 1 FDA reports)
AGEUSIA ( 1 FDA reports)
AIDS ENCEPHALOPATHY ( 1 FDA reports)
ALBUMIN GLOBULIN RATIO ABNORMAL ( 1 FDA reports)
ALVEOLITIS ALLERGIC ( 1 FDA reports)
ANAEMIA MACROCYTIC ( 1 FDA reports)
ANAEMIA POSTOPERATIVE ( 1 FDA reports)
ANAL FISTULA ( 1 FDA reports)
ANAL ULCER ( 1 FDA reports)
ANASTOMOTIC ULCER ( 1 FDA reports)
ANGIOFIBROMA ( 1 FDA reports)
ANGIONEUROTIC OEDEMA ( 1 FDA reports)
ANION GAP INCREASED ( 1 FDA reports)
ANORECTAL INFECTION ( 1 FDA reports)
ANURIA ( 1 FDA reports)
AORTIC ATHEROSCLEROSIS ( 1 FDA reports)
AORTIC VALVE REPAIR ( 1 FDA reports)
APATHY ( 1 FDA reports)
APHAGIA ( 1 FDA reports)
APLASTIC ANAEMIA ( 1 FDA reports)
APPARENT LIFE THREATENING EVENT ( 1 FDA reports)
APPLICATION SITE ERYTHEMA ( 1 FDA reports)
ARTERIAL THROMBOSIS ( 1 FDA reports)
ARTERIOSPASM CORONARY ( 1 FDA reports)
ASPIRATION PLEURAL CAVITY ABNORMAL ( 1 FDA reports)
ASTIGMATISM ( 1 FDA reports)
ATRIOVENTRICULAR BLOCK ( 1 FDA reports)
BACTERIA STOOL IDENTIFIED ( 1 FDA reports)
BACTERIA URINE ( 1 FDA reports)
BILE DUCT OBSTRUCTION ( 1 FDA reports)
BILE DUCT STENOSIS ( 1 FDA reports)
BILE DUCT STONE ( 1 FDA reports)
BILIARY DILATATION ( 1 FDA reports)
BIOPSY PALATE ABNORMAL ( 1 FDA reports)
BLADDER DYSFUNCTION ( 1 FDA reports)
BLAST CELL CRISIS ( 1 FDA reports)
BLEEDING VARICOSE VEIN ( 1 FDA reports)
BLINDNESS CORTICAL ( 1 FDA reports)
BLOOD BICARBONATE INCREASED ( 1 FDA reports)
BLOOD CALCIUM INCREASED ( 1 FDA reports)
BLOOD COUNT ABNORMAL ( 1 FDA reports)
BLOOD CREATINE INCREASED ( 1 FDA reports)
BLOOD CREATININE DECREASED ( 1 FDA reports)
BLOOD HUMAN CHORIONIC GONADOTROPIN INCREASED ( 1 FDA reports)
BLOOD MAGNESIUM ABNORMAL ( 1 FDA reports)
BLOOD MAGNESIUM INCREASED ( 1 FDA reports)
BLOOD POTASSIUM ABNORMAL ( 1 FDA reports)
BLOOD PRESSURE SYSTOLIC DECREASED ( 1 FDA reports)
BLOOD THYROID STIMULATING HORMONE DECREASED ( 1 FDA reports)
BLOOD UREA NITROGEN/CREATININE RATIO INCREASED ( 1 FDA reports)
BLOOD URINE ( 1 FDA reports)
BODY TEMPERATURE FLUCTUATION ( 1 FDA reports)
BONE MARROW MYELOGRAM ABNORMAL ( 1 FDA reports)
BRAIN NATRIURETIC PEPTIDE INCREASED ( 1 FDA reports)
BREAKTHROUGH PAIN ( 1 FDA reports)
BREAST ABSCESS ( 1 FDA reports)
BREAST CANCER STAGE IV ( 1 FDA reports)
BREAST CELLULITIS ( 1 FDA reports)
BREATH SOUNDS ABSENT ( 1 FDA reports)
BURNS THIRD DEGREE ( 1 FDA reports)
BURSITIS ( 1 FDA reports)
CAECITIS ( 1 FDA reports)
CAMPYLOBACTER TEST POSITIVE ( 1 FDA reports)
CARDIAC FAILURE ( 1 FDA reports)
CARDIAC FAILURE ACUTE ( 1 FDA reports)
CARDIAC FAILURE HIGH OUTPUT ( 1 FDA reports)
CARDIAC FLUTTER ( 1 FDA reports)
CARDIAC MURMUR ( 1 FDA reports)
CATHETER SITE CELLULITIS ( 1 FDA reports)
CATHETER SITE ERYTHEMA ( 1 FDA reports)
CATHETER SITE NECROSIS ( 1 FDA reports)
CD4 LYMPHOCYTES DECREASED ( 1 FDA reports)
CEREBRAL ARTERY EMBOLISM ( 1 FDA reports)
CHALAZION ( 1 FDA reports)
CHEMICAL INJURY ( 1 FDA reports)
CHEMOTHERAPY ( 1 FDA reports)
CHOKING ( 1 FDA reports)
CHOLANGITIS ( 1 FDA reports)
CHOLANGITIS SUPPURATIVE ( 1 FDA reports)
CHOLESTASIS ( 1 FDA reports)
CHROMATURIA ( 1 FDA reports)
CLOSTRIDIUM COLITIS ( 1 FDA reports)
COLONIC HAEMORRHAGE ( 1 FDA reports)
COLONIC OBSTRUCTION ( 1 FDA reports)
COLONIC STENOSIS ( 1 FDA reports)
COLORECTAL CANCER METASTATIC ( 1 FDA reports)
COMPUTERISED TOMOGRAM ABDOMEN ABNORMAL ( 1 FDA reports)
CONJUNCTIVITIS VIRAL ( 1 FDA reports)
CORNEAL ABRASION ( 1 FDA reports)
CRACKLES LUNG ( 1 FDA reports)
DEFAECATION URGENCY ( 1 FDA reports)
DEMENTIA ( 1 FDA reports)
DENTAL NECROSIS ( 1 FDA reports)
DENTAL PROSTHESIS USER ( 1 FDA reports)
DENTAL TREATMENT ( 1 FDA reports)
DEPRESSION SUICIDAL ( 1 FDA reports)
DERMATITIS ALLERGIC ( 1 FDA reports)
DERMATITIS EXFOLIATIVE ( 1 FDA reports)
DEVICE DEPLOYMENT ISSUE ( 1 FDA reports)
DIABETIC NEUROPATHY ( 1 FDA reports)
DIAPHRAGMATIC DISORDER ( 1 FDA reports)
DILATATION VENTRICULAR ( 1 FDA reports)
DROOLING ( 1 FDA reports)
DRUG DOSE OMISSION ( 1 FDA reports)
DRUG LEVEL DECREASED ( 1 FDA reports)
DRUG LEVEL INCREASED ( 1 FDA reports)
DYSAESTHESIA ( 1 FDA reports)
DYSAESTHESIA PHARYNX ( 1 FDA reports)
DYSENTERY ( 1 FDA reports)
EAR CONGESTION ( 1 FDA reports)
EAR DISCOMFORT ( 1 FDA reports)
ECHOCARDIOGRAM ABNORMAL ( 1 FDA reports)
EDENTULOUS ( 1 FDA reports)
ELECTROCARDIOGRAM ABNORMAL ( 1 FDA reports)
ELECTROCARDIOGRAM ST SEGMENT ELEVATION ( 1 FDA reports)
ELECTROCARDIOGRAM ST-T CHANGE ( 1 FDA reports)
ELECTROCARDIOGRAM ST-T SEGMENT ABNORMAL ( 1 FDA reports)
ELECTROCARDIOGRAM T WAVE PEAKED ( 1 FDA reports)
ENDOCARDITIS ( 1 FDA reports)
ENERGY INCREASED ( 1 FDA reports)
ENTERITIS INFECTIOUS ( 1 FDA reports)
ENTEROBACTER SEPSIS ( 1 FDA reports)
ENTEROCOLITIS HAEMORRHAGIC ( 1 FDA reports)
ENTEROCOLITIS INFECTIOUS ( 1 FDA reports)
ENTEROCUTANEOUS FISTULA ( 1 FDA reports)
EOSINOPHILIA ( 1 FDA reports)
ESCHERICHIA URINARY TRACT INFECTION ( 1 FDA reports)
EXSANGUINATION ( 1 FDA reports)
EYE IRRITATION ( 1 FDA reports)
EYE PRURITUS ( 1 FDA reports)
FAECAL VOLUME DECREASED ( 1 FDA reports)
FAECALOMA ( 1 FDA reports)
FEAR ( 1 FDA reports)
FEELING JITTERY ( 1 FDA reports)
FIBROCYSTIC BREAST DISEASE ( 1 FDA reports)
FOOD ALLERGY ( 1 FDA reports)
FOOD INTOLERANCE ( 1 FDA reports)
FOREIGN BODY REACTION ( 1 FDA reports)
FOREIGN BODY TRAUMA ( 1 FDA reports)
FRACTURE ( 1 FDA reports)
GASTRIC CANCER ( 1 FDA reports)
GASTRIC POLYPS ( 1 FDA reports)
GASTRIC ULCER PERFORATION ( 1 FDA reports)
GASTRIC VARICES ( 1 FDA reports)
GASTROENTERITIS RADIATION ( 1 FDA reports)
GENITAL BURNING SENSATION ( 1 FDA reports)
GENITAL HERPES ( 1 FDA reports)
GENITAL RASH ( 1 FDA reports)
GINGIVAL DISCOLOURATION ( 1 FDA reports)
GLIOBLASTOMA ( 1 FDA reports)
GLOSSITIS ( 1 FDA reports)
GLYCOSYLATED HAEMOGLOBIN INCREASED ( 1 FDA reports)
GRANULOCYTE COUNT DECREASED ( 1 FDA reports)
GRIP STRENGTH DECREASED ( 1 FDA reports)
HAEMANGIOMA OF LIVER ( 1 FDA reports)
HAEMARTHROSIS ( 1 FDA reports)
HAEMATOCRIT INCREASED ( 1 FDA reports)
HAEMODYNAMIC INSTABILITY ( 1 FDA reports)
HAEMOGLOBIN ABNORMAL ( 1 FDA reports)
HAEMOGLOBIN INCREASED ( 1 FDA reports)
HAEMOGLOBIN S DECREASED ( 1 FDA reports)
HAEMOGLOBINURIA ( 1 FDA reports)
HAND FRACTURE ( 1 FDA reports)
HEARING IMPAIRED ( 1 FDA reports)
HEART RATE DECREASED ( 1 FDA reports)
HELICOBACTER INFECTION ( 1 FDA reports)
HEPATIC FIBROSIS ( 1 FDA reports)
HEPATIC HAEMATOMA ( 1 FDA reports)
HEPATIC MASS ( 1 FDA reports)
HEPATOCELLULAR INJURY ( 1 FDA reports)
HYPERAEMIA ( 1 FDA reports)
HYPERCALCAEMIA OF MALIGNANCY ( 1 FDA reports)
HYPERCHROMIC ANAEMIA ( 1 FDA reports)
HYPERCOAGULATION ( 1 FDA reports)
HYPERTENSIVE CRISIS ( 1 FDA reports)
HYPERTHYROIDISM ( 1 FDA reports)
HYPERTRICHOSIS ( 1 FDA reports)
HYPERTROPHIC SCAR ( 1 FDA reports)
HYPERVENTILATION ( 1 FDA reports)
HYPOCHLORAEMIA ( 1 FDA reports)
HYPOGLYCAEMIC COMA ( 1 FDA reports)
HYPOKINESIA ( 1 FDA reports)
HYPOPNOEA ( 1 FDA reports)
HYPOTRICHOSIS ( 1 FDA reports)
HYPOVENTILATION ( 1 FDA reports)
HYPOXIC-ISCHAEMIC ENCEPHALOPATHY ( 1 FDA reports)
IDIOPATHIC THROMBOCYTOPENIC PURPURA ( 1 FDA reports)
IMMOBILE ( 1 FDA reports)
IMMUNE RECONSTITUTION SYNDROME ( 1 FDA reports)
IMPAIRED WORK ABILITY ( 1 FDA reports)
INCOHERENT ( 1 FDA reports)
INCORRECT DRUG ADMINISTRATION DURATION ( 1 FDA reports)
INDURATION ( 1 FDA reports)
INFLAMMATION LOCALISED ( 1 FDA reports)
INFUSION SITE BURNING ( 1 FDA reports)
INFUSION SITE DISCOLOURATION ( 1 FDA reports)
INFUSION SITE HAEMATOMA ( 1 FDA reports)
INFUSION SITE INDURATION ( 1 FDA reports)
INJECTION SITE CELLULITIS ( 1 FDA reports)
INJECTION SITE DISCOMFORT ( 1 FDA reports)
INJECTION SITE VESICLES ( 1 FDA reports)
INTESTINAL GANGRENE ( 1 FDA reports)
INTESTINAL ULCER PERFORATION ( 1 FDA reports)
INTRAVASCULAR HAEMOLYSIS ( 1 FDA reports)
IRON DEFICIENCY ANAEMIA ( 1 FDA reports)
ISCHAEMIA ( 1 FDA reports)
ISCHAEMIC ULCER ( 1 FDA reports)
JOINT LOCK ( 1 FDA reports)
KERATITIS BACTERIAL ( 1 FDA reports)
KLEBSIELLA INFECTION ( 1 FDA reports)
LARGE INTESTINAL ULCER HAEMORRHAGE ( 1 FDA reports)
LEUKOCYTOCLASTIC VASCULITIS ( 1 FDA reports)
LEUKOPLAKIA ( 1 FDA reports)
LIP DRY ( 1 FDA reports)
LIP OEDEMA ( 1 FDA reports)
LOBAR PNEUMONIA ( 1 FDA reports)
LOCALISED INFECTION ( 1 FDA reports)
LUNG ADENOCARCINOMA RECURRENT ( 1 FDA reports)
LUNG ADENOCARCINOMA STAGE IV ( 1 FDA reports)
LUNG CANCER METASTATIC ( 1 FDA reports)
LUNG CONSOLIDATION ( 1 FDA reports)
LUNG INFECTION ( 1 FDA reports)
LYMPH NODE CANCER METASTATIC ( 1 FDA reports)
MALIGNANT PERITONEAL NEOPLASM ( 1 FDA reports)
MEAN CELL VOLUME ABNORMAL ( 1 FDA reports)
MENINGITIS CRYPTOCOCCAL ( 1 FDA reports)
MESOTHELIOMA ( 1 FDA reports)
METASTASES TO ADRENALS ( 1 FDA reports)
METASTASES TO BONE MARROW ( 1 FDA reports)
METASTASES TO NECK ( 1 FDA reports)
METASTASES TO OESOPHAGUS ( 1 FDA reports)
MIDDLE INSOMNIA ( 1 FDA reports)
MIGRAINE WITH AURA ( 1 FDA reports)
MITRAL VALVE DISEASE ( 1 FDA reports)
MOANING ( 1 FDA reports)
MOBILITY DECREASED ( 1 FDA reports)
MOTOR DYSFUNCTION ( 1 FDA reports)
MUCOSAL DRYNESS ( 1 FDA reports)
MUSCLE HAEMORRHAGE ( 1 FDA reports)
MYDRIASIS ( 1 FDA reports)
MYODESOPSIA ( 1 FDA reports)
MYOPIA ( 1 FDA reports)
N-TERMINAL PROHORMONE BRAIN NATRIURETIC PEPTIDE ( 1 FDA reports)
NAIL DISCOLOURATION ( 1 FDA reports)
NEURILEMMOMA MALIGNANT ( 1 FDA reports)
NEUROLOGICAL EXAMINATION ABNORMAL ( 1 FDA reports)
NEUROLOGICAL SYMPTOM ( 1 FDA reports)
NEUTROPHIL COUNT ( 1 FDA reports)
NEUTROPHIL COUNT ABNORMAL ( 1 FDA reports)
NEUTROPHIL PERCENTAGE DECREASED ( 1 FDA reports)
NEUTROPHILIA ( 1 FDA reports)
NON-HODGKIN'S LYMPHOMA RECURRENT ( 1 FDA reports)
NON-HODGKIN'S LYMPHOMA REFRACTORY ( 1 FDA reports)
NUCLEAR MAGNETIC RESONANCE IMAGING BRAIN ABNORMAL ( 1 FDA reports)
OESOPHAGEAL CANDIDIASIS ( 1 FDA reports)
OESOPHAGEAL OBSTRUCTION ( 1 FDA reports)
OESOPHAGEAL SPASM ( 1 FDA reports)
OESOPHAGEAL VARICES HAEMORRHAGE ( 1 FDA reports)
OLIGURIA ( 1 FDA reports)
ONCOLOGIC COMPLICATION ( 1 FDA reports)
ONYCHORRHEXIS ( 1 FDA reports)
OPPORTUNISTIC INFECTION ( 1 FDA reports)
ORAL MUCOSAL BLISTERING ( 1 FDA reports)
OROPHARYNGEAL BLISTERING ( 1 FDA reports)
OTOTOXICITY ( 1 FDA reports)
OVARIAN ADENOMA ( 1 FDA reports)
OVARIAN CANCER ( 1 FDA reports)
OXYGEN SATURATION ABNORMAL ( 1 FDA reports)
PAINFUL RESPIRATION ( 1 FDA reports)
PANCREATIC CARCINOMA METASTATIC ( 1 FDA reports)
PANIC REACTION ( 1 FDA reports)
PAPULE ( 1 FDA reports)
PARAPARESIS ( 1 FDA reports)
PARTIAL SEIZURES ( 1 FDA reports)
PELVIC FLUID COLLECTION ( 1 FDA reports)
PERFORATED ULCER ( 1 FDA reports)
PERIPHERAL SENSORIMOTOR NEUROPATHY ( 1 FDA reports)
PERITONEAL CARCINOMA ( 1 FDA reports)
PERITONEAL INFECTION ( 1 FDA reports)
PHARYNGEAL ERYTHEMA ( 1 FDA reports)
PHARYNGEAL STENOSIS ( 1 FDA reports)
PHOTODERMATOSIS ( 1 FDA reports)
PLASMA CELLS DECREASED ( 1 FDA reports)
PLASTIC SURGERY TO THE FACE ( 1 FDA reports)
PLEURAL INFECTION ( 1 FDA reports)
PLEURAL NEOPLASM ( 1 FDA reports)
PNEUMATOSIS CYSTOIDES INTESTINALIS ( 1 FDA reports)
PNEUMOPERITONEUM ( 1 FDA reports)
PO2 DECREASED ( 1 FDA reports)
PORTAL VEIN THROMBOSIS ( 1 FDA reports)
POST HERPETIC NEURALGIA ( 1 FDA reports)
POST PROCEDURAL DIARRHOEA ( 1 FDA reports)
POST PROCEDURAL NAUSEA ( 1 FDA reports)
POST PROCEDURAL VOMITING ( 1 FDA reports)
POSTICTAL STATE ( 1 FDA reports)
POSTOPERATIVE ABSCESS ( 1 FDA reports)
POSTURE ABNORMAL ( 1 FDA reports)
PREGNANCY ( 1 FDA reports)
PRESBYOPIA ( 1 FDA reports)
PROCEDURAL SITE REACTION ( 1 FDA reports)
PRODUCT SUBSTITUTION ISSUE ( 1 FDA reports)
PROSTATE CANCER ( 1 FDA reports)
PROTEIN URINE PRESENT ( 1 FDA reports)
PSEUDOMONAL BACTERAEMIA ( 1 FDA reports)
PSEUDOMONAS INFECTION ( 1 FDA reports)
PSYCHOMOTOR HYPERACTIVITY ( 1 FDA reports)
PULMONARY HAEMORRHAGE ( 1 FDA reports)
PULMONARY HILUM MASS ( 1 FDA reports)
PUPILLARY REFLEX IMPAIRED ( 1 FDA reports)
PYELONEPHRITIS ACUTE ( 1 FDA reports)
RADIATION DYSPHAGIA ( 1 FDA reports)
RADIATION PNEUMONITIS ( 1 FDA reports)
RADIOTHERAPY ( 1 FDA reports)
RECTAL CANCER METASTATIC ( 1 FDA reports)
RECTAL TENESMUS ( 1 FDA reports)
RED BLOOD CELL ABNORMALITY ( 1 FDA reports)
RED BLOOD CELLS URINE ( 1 FDA reports)
REFRACTION DISORDER ( 1 FDA reports)
REFRACTORY CYTOPENIA WITH MULTILINEAGE DYSPLASIA ( 1 FDA reports)
REFUSAL OF TREATMENT BY RELATIVE ( 1 FDA reports)
RESPIRATORY DEPRESSION ( 1 FDA reports)
RETICULOCYTE COUNT INCREASED ( 1 FDA reports)
RETROPERITONEAL LYMPHADENOPATHY ( 1 FDA reports)
RHINALGIA ( 1 FDA reports)
RIGHT VENTRICULAR DYSFUNCTION ( 1 FDA reports)
SCOTOMA ( 1 FDA reports)
SELF-MEDICATION ( 1 FDA reports)
SENSORY LOSS ( 1 FDA reports)
SKIN HAEMORRHAGE ( 1 FDA reports)
SKIN IRRITATION ( 1 FDA reports)
SKIN NECROSIS ( 1 FDA reports)
SKIN NEOPLASM EXCISION ( 1 FDA reports)
SKIN NODULE ( 1 FDA reports)
SKIN REACTION ( 1 FDA reports)
SKIN SWELLING ( 1 FDA reports)
SKIN WARM ( 1 FDA reports)
SKIN WRINKLING ( 1 FDA reports)
SMALL CELL LUNG CANCER STAGE UNSPECIFIED ( 1 FDA reports)
SOFT TISSUE INFECTION ( 1 FDA reports)
SPINAL CORD INFARCTION ( 1 FDA reports)
SPLENIC INFARCTION ( 1 FDA reports)
SPLENIC RUPTURE ( 1 FDA reports)
SPUTUM ABNORMAL ( 1 FDA reports)
SPUTUM CULTURE POSITIVE ( 1 FDA reports)
STARING ( 1 FDA reports)
STREPTOCOCCAL SEPSIS ( 1 FDA reports)
STUPOR ( 1 FDA reports)
SUBCLAVIAN VEIN THROMBOSIS ( 1 FDA reports)
SUBCUTANEOUS ABSCESS ( 1 FDA reports)
SUBCUTANEOUS EMPHYSEMA ( 1 FDA reports)
SUBILEUS ( 1 FDA reports)
SUDDEN CARDIAC DEATH ( 1 FDA reports)
SUDDEN DEATH ( 1 FDA reports)
SUDDEN ONSET OF SLEEP ( 1 FDA reports)
SUDDEN VISUAL LOSS ( 1 FDA reports)
SUPERIOR VENA CAVAL OCCLUSION ( 1 FDA reports)
SUPRAPUBIC PAIN ( 1 FDA reports)
SUPRAVENTRICULAR TACHYARRHYTHMIA ( 1 FDA reports)
SYSTEMIC INFLAMMATORY RESPONSE SYNDROME ( 1 FDA reports)
TERMINAL INSOMNIA ( 1 FDA reports)
THERMAL BURN ( 1 FDA reports)
THIRST ( 1 FDA reports)
THROAT CANCER ( 1 FDA reports)
THROMBOTIC MICROANGIOPATHY ( 1 FDA reports)
THYROID DISORDER ( 1 FDA reports)
TONGUE BLISTERING ( 1 FDA reports)
TONIC CLONIC MOVEMENTS ( 1 FDA reports)
TOXIC ENCEPHALOPATHY ( 1 FDA reports)
TOXIC NODULAR GOITRE ( 1 FDA reports)
TRANSAMINASES INCREASED ( 1 FDA reports)
TRICHIASIS ( 1 FDA reports)
TROPONIN I INCREASED ( 1 FDA reports)
TUMOUR HAEMORRHAGE ( 1 FDA reports)
TUNNEL VISION ( 1 FDA reports)
TYPE IV HYPERSENSITIVITY REACTION ( 1 FDA reports)
URINE ABNORMALITY ( 1 FDA reports)
URINE KETONE BODY PRESENT ( 1 FDA reports)
URINE ODOUR ABNORMAL ( 1 FDA reports)
URTICARIA GENERALISED ( 1 FDA reports)
VAGINAL CANDIDIASIS ( 1 FDA reports)
VAGINAL ULCERATION ( 1 FDA reports)
VASOSPASM ( 1 FDA reports)
VENA CAVA THROMBOSIS ( 1 FDA reports)
VENOUS OCCLUSION ( 1 FDA reports)
VENTRICULAR ARRHYTHMIA ( 1 FDA reports)
VENTRICULAR DYSFUNCTION ( 1 FDA reports)
VENTRICULAR HYPOKINESIA ( 1 FDA reports)
VIITH NERVE PARALYSIS ( 1 FDA reports)
VITREOUS DEGENERATION ( 1 FDA reports)
VULVITIS ( 1 FDA reports)
VULVOVAGINAL DISCOMFORT ( 1 FDA reports)
WHITE BLOOD CELL COUNT ABNORMAL ( 1 FDA reports)
WOUND INFECTION ( 1 FDA reports)

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