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

DRUG INTERACTION ( 76 FDA reports)
NAUSEA ( 75 FDA reports)
DYSPNOEA ( 67 FDA reports)
ARTHRALGIA ( 65 FDA reports)
DRUG INEFFECTIVE ( 63 FDA reports)
PNEUMONIA ( 59 FDA reports)
PAIN ( 58 FDA reports)
OEDEMA PERIPHERAL ( 53 FDA reports)
FATIGUE ( 49 FDA reports)
VOMITING ( 48 FDA reports)
DIARRHOEA ( 47 FDA reports)
RHEUMATOID ARTHRITIS ( 46 FDA reports)
PAIN IN EXTREMITY ( 45 FDA reports)
RENAL FAILURE ACUTE ( 44 FDA reports)
ANAEMIA ( 42 FDA reports)
DIZZINESS ( 41 FDA reports)
GENERAL PHYSICAL HEALTH DETERIORATION ( 41 FDA reports)
HEADACHE ( 39 FDA reports)
SOMNOLENCE ( 39 FDA reports)
MALAISE ( 38 FDA reports)
PYREXIA ( 37 FDA reports)
WEIGHT DECREASED ( 33 FDA reports)
HYPERTENSION ( 31 FDA reports)
OSTEONECROSIS ( 31 FDA reports)
ABDOMINAL PAIN ( 30 FDA reports)
CONDITION AGGRAVATED ( 30 FDA reports)
PULMONARY EMBOLISM ( 29 FDA reports)
CHEST PAIN ( 28 FDA reports)
JOINT SWELLING ( 28 FDA reports)
SEPSIS ( 28 FDA reports)
ABDOMINAL PAIN UPPER ( 27 FDA reports)
GASTROINTESTINAL HAEMORRHAGE ( 27 FDA reports)
BACK PAIN ( 26 FDA reports)
CARDIAC FAILURE ( 26 FDA reports)
ASTHENIA ( 25 FDA reports)
DECREASED APPETITE ( 25 FDA reports)
HYPOTENSION ( 25 FDA reports)
PLEURAL EFFUSION ( 25 FDA reports)
TACHYCARDIA ( 25 FDA reports)
RASH ( 24 FDA reports)
WEIGHT INCREASED ( 24 FDA reports)
IMPAIRED HEALING ( 23 FDA reports)
DEATH ( 22 FDA reports)
DEHYDRATION ( 22 FDA reports)
GAIT DISTURBANCE ( 22 FDA reports)
PARAESTHESIA ( 22 FDA reports)
CONFUSIONAL STATE ( 21 FDA reports)
MELAENA ( 20 FDA reports)
PANCYTOPENIA ( 20 FDA reports)
C-REACTIVE PROTEIN INCREASED ( 19 FDA reports)
DEPRESSION ( 19 FDA reports)
DEEP VEIN THROMBOSIS ( 18 FDA reports)
PRURITUS ( 18 FDA reports)
URINARY TRACT INFECTION ( 18 FDA reports)
BLOOD CHOLESTEROL INCREASED ( 17 FDA reports)
BLOOD CREATININE INCREASED ( 17 FDA reports)
CONSTIPATION ( 17 FDA reports)
DUODENAL ULCER ( 17 FDA reports)
GASTRITIS ( 17 FDA reports)
HYPERHIDROSIS ( 17 FDA reports)
INSOMNIA ( 17 FDA reports)
PALPITATIONS ( 17 FDA reports)
ATRIAL FIBRILLATION ( 16 FDA reports)
DRUG EFFECT DECREASED ( 16 FDA reports)
FALL ( 16 FDA reports)
GAMMA-GLUTAMYLTRANSFERASE INCREASED ( 16 FDA reports)
HYPOKALAEMIA ( 16 FDA reports)
INFUSION RELATED REACTION ( 16 FDA reports)
MYOCARDIAL INFARCTION ( 16 FDA reports)
OSTEOARTHRITIS ( 16 FDA reports)
RENAL FAILURE ( 16 FDA reports)
AGEUSIA ( 15 FDA reports)
ALOPECIA ( 15 FDA reports)
ARTHRITIS ( 15 FDA reports)
CHOLELITHIASIS ( 15 FDA reports)
DYSPEPSIA ( 15 FDA reports)
HAEMATEMESIS ( 15 FDA reports)
HAEMATOMA ( 15 FDA reports)
HAEMOGLOBIN DECREASED ( 15 FDA reports)
MUSCLE SPASMS ( 15 FDA reports)
SPEECH DISORDER ( 15 FDA reports)
STRESS ( 15 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 14 FDA reports)
CEREBROVASCULAR ACCIDENT ( 14 FDA reports)
HYPERSENSITIVITY ( 14 FDA reports)
LYMPHADENOPATHY ( 14 FDA reports)
COUGH ( 13 FDA reports)
DRUG HYPERSENSITIVITY ( 13 FDA reports)
HAEMATURIA ( 13 FDA reports)
HYPOAESTHESIA ( 13 FDA reports)
RESTLESSNESS ( 13 FDA reports)
THROMBOCYTOPENIA ( 13 FDA reports)
CHILLS ( 12 FDA reports)
DISORIENTATION ( 12 FDA reports)
DYSPNOEA EXERTIONAL ( 12 FDA reports)
ERYTHEMA ( 12 FDA reports)
FLUSHING ( 12 FDA reports)
KNEE ARTHROPLASTY ( 12 FDA reports)
LEUKOPENIA ( 12 FDA reports)
LOWER RESPIRATORY TRACT INFECTION ( 12 FDA reports)
NEPHROLITHIASIS ( 12 FDA reports)
RENAL FAILURE CHRONIC ( 12 FDA reports)
SYSTEMIC LUPUS ERYTHEMATOSUS ( 12 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 11 FDA reports)
BRADYCARDIA ( 11 FDA reports)
CROHN'S DISEASE ( 11 FDA reports)
DYSGEUSIA ( 11 FDA reports)
HEPATIC STEATOSIS ( 11 FDA reports)
LETHARGY ( 11 FDA reports)
NEPHROTIC SYNDROME ( 11 FDA reports)
OEDEMA ( 11 FDA reports)
SENSORY DISTURBANCE ( 11 FDA reports)
VISUAL IMPAIRMENT ( 11 FDA reports)
CIRCULATORY COLLAPSE ( 10 FDA reports)
CONVULSION ( 10 FDA reports)
DRUG INTOLERANCE ( 10 FDA reports)
FACTOR VIII INHIBITION ( 10 FDA reports)
GASTRIC ULCER ( 10 FDA reports)
HYPERTENSIVE HEART DISEASE ( 10 FDA reports)
INFECTION ( 10 FDA reports)
LIVER FUNCTION TEST ABNORMAL ( 10 FDA reports)
LOSS OF CONSCIOUSNESS ( 10 FDA reports)
MUSCULAR WEAKNESS ( 10 FDA reports)
MUSCULOSKELETAL PAIN ( 10 FDA reports)
MYALGIA ( 10 FDA reports)
NASOPHARYNGITIS ( 10 FDA reports)
PANCREATITIS ( 10 FDA reports)
PHARYNGITIS ( 10 FDA reports)
POSTOPERATIVE WOUND INFECTION ( 10 FDA reports)
PROSTATIC SPECIFIC ANTIGEN INCREASED ( 10 FDA reports)
PURULENT DISCHARGE ( 10 FDA reports)
ROAD TRAFFIC ACCIDENT ( 10 FDA reports)
SLEEP DISORDER ( 10 FDA reports)
SUICIDAL IDEATION ( 10 FDA reports)
SUICIDE ATTEMPT ( 10 FDA reports)
SYNCOPE ( 10 FDA reports)
URINARY RETENTION ( 10 FDA reports)
URTICARIA ( 10 FDA reports)
VISUAL DISTURBANCE ( 10 FDA reports)
ANXIETY ( 9 FDA reports)
CHROMATURIA ( 9 FDA reports)
GASTRITIS EROSIVE ( 9 FDA reports)
JOINT ARTHROPLASTY ( 9 FDA reports)
LOCALISED INFECTION ( 9 FDA reports)
PERIPHERAL COLDNESS ( 9 FDA reports)
PRESYNCOPE ( 9 FDA reports)
RESPIRATORY FAILURE ( 9 FDA reports)
VERTIGO ( 9 FDA reports)
VISION BLURRED ( 9 FDA reports)
AGGRESSION ( 8 FDA reports)
ANAPHYLACTIC REACTION ( 8 FDA reports)
ANKYLOSING SPONDYLITIS ( 8 FDA reports)
BLOOD ALKALINE PHOSPHATASE INCREASED ( 8 FDA reports)
BLOOD PRESSURE INCREASED ( 8 FDA reports)
BONE DISORDER ( 8 FDA reports)
CARTILAGE INJURY ( 8 FDA reports)
COLITIS ( 8 FDA reports)
ERYSIPELAS ( 8 FDA reports)
FACE INJURY ( 8 FDA reports)
GASTRIC ULCER HAEMORRHAGE ( 8 FDA reports)
HALLUCINATION ( 8 FDA reports)
HAND DEFORMITY ( 8 FDA reports)
HEPATIC PAIN ( 8 FDA reports)
HEPATITIS ( 8 FDA reports)
INTERVERTEBRAL DISC PROTRUSION ( 8 FDA reports)
MOUTH INJURY ( 8 FDA reports)
PELVIC FRACTURE ( 8 FDA reports)
PNEUMONITIS ( 8 FDA reports)
PSORIATIC ARTHROPATHY ( 8 FDA reports)
SINUSITIS ( 8 FDA reports)
SWELLING ( 8 FDA reports)
TUBERCULOSIS ( 8 FDA reports)
VASCULITIS ( 8 FDA reports)
AGITATION ( 7 FDA reports)
ASTHMA ( 7 FDA reports)
BLOOD CREATINE PHOSPHOKINASE INCREASED ( 7 FDA reports)
BLOOD GLUCOSE INCREASED ( 7 FDA reports)
BLOOD TRIGLYCERIDES INCREASED ( 7 FDA reports)
CARDIAC ARREST ( 7 FDA reports)
CARDIAC DISORDER ( 7 FDA reports)
DIABETES MELLITUS INADEQUATE CONTROL ( 7 FDA reports)
DRUG ABUSE ( 7 FDA reports)
DYSPHAGIA ( 7 FDA reports)
ECZEMA ( 7 FDA reports)
ELECTROCARDIOGRAM T WAVE INVERSION ( 7 FDA reports)
FEELING ABNORMAL ( 7 FDA reports)
HERPES ZOSTER ( 7 FDA reports)
HYPOCALCAEMIA ( 7 FDA reports)
HYPOGLYCAEMIA ( 7 FDA reports)
INFLUENZA LIKE ILLNESS ( 7 FDA reports)
INTERNATIONAL NORMALISED RATIO INCREASED ( 7 FDA reports)
JOINT STIFFNESS ( 7 FDA reports)
MASS ( 7 FDA reports)
MIGRAINE ( 7 FDA reports)
PAIN IN JAW ( 7 FDA reports)
PLEURISY ( 7 FDA reports)
PNEUMOTHORAX ( 7 FDA reports)
PSORIASIS ( 7 FDA reports)
RENAL IMPAIRMENT ( 7 FDA reports)
SKIN EXFOLIATION ( 7 FDA reports)
STAPHYLOCOCCAL INFECTION ( 7 FDA reports)
TACHYARRHYTHMIA ( 7 FDA reports)
TENDON RUPTURE ( 7 FDA reports)
TREMOR ( 7 FDA reports)
VARICOSE VEIN ( 7 FDA reports)
WITHDRAWAL SYNDROME ( 7 FDA reports)
ABSCESS JAW ( 6 FDA reports)
ACUTE HEPATIC FAILURE ( 6 FDA reports)
AMNESIA ( 6 FDA reports)
ANAL ABSCESS ( 6 FDA reports)
ANOSMIA ( 6 FDA reports)
AORTIC VALVE INCOMPETENCE ( 6 FDA reports)
APHASIA ( 6 FDA reports)
ARRHYTHMIA ( 6 FDA reports)
ASCITES ( 6 FDA reports)
BLOOD PRESSURE FLUCTUATION ( 6 FDA reports)
BLOOD PRODUCT TRANSFUSION DEPENDENT ( 6 FDA reports)
BONE PAIN ( 6 FDA reports)
BRAIN NEOPLASM ( 6 FDA reports)
BURNING SENSATION ( 6 FDA reports)
CLOSTRIDIAL INFECTION ( 6 FDA reports)
COGNITIVE DISORDER ( 6 FDA reports)
CONGESTIVE CARDIOMYOPATHY ( 6 FDA reports)
DERMATITIS PSORIASIFORM ( 6 FDA reports)
DISTURBANCE IN ATTENTION ( 6 FDA reports)
ELECTROLYTE IMBALANCE ( 6 FDA reports)
ENCEPHALOPATHY ( 6 FDA reports)
ESCHERICHIA URINARY TRACT INFECTION ( 6 FDA reports)
HAEMOPTYSIS ( 6 FDA reports)
HEPATITIS ACUTE ( 6 FDA reports)
HEPATITIS TOXIC ( 6 FDA reports)
HIP SURGERY ( 6 FDA reports)
HYPOMAGNESAEMIA ( 6 FDA reports)
HYPONATRAEMIA ( 6 FDA reports)
HYPOXIA ( 6 FDA reports)
INFLAMMATION ( 6 FDA reports)
INJECTION SITE PRURITUS ( 6 FDA reports)
INJECTION SITE SWELLING ( 6 FDA reports)
JOINT EFFUSION ( 6 FDA reports)
LABORATORY TEST ABNORMAL ( 6 FDA reports)
LISTLESS ( 6 FDA reports)
LUNG ADENOCARCINOMA ( 6 FDA reports)
LUNG NEOPLASM MALIGNANT ( 6 FDA reports)
MALIGNANT NEOPLASM PROGRESSION ( 6 FDA reports)
MYOCARDIAL ISCHAEMIA ( 6 FDA reports)
NEPHROGENIC ANAEMIA ( 6 FDA reports)
NIGHT SWEATS ( 6 FDA reports)
PALLOR ( 6 FDA reports)
PELVIC VENOUS THROMBOSIS ( 6 FDA reports)
PHOTOPHOBIA ( 6 FDA reports)
PLATELET COUNT DECREASED ( 6 FDA reports)
PLEURITIC PAIN ( 6 FDA reports)
PRODUCTIVE COUGH ( 6 FDA reports)
PROSTATE CANCER ( 6 FDA reports)
PRURITUS GENERALISED ( 6 FDA reports)
PULMONARY OEDEMA ( 6 FDA reports)
RASH PRURITIC ( 6 FDA reports)
RECTAL HAEMORRHAGE ( 6 FDA reports)
RIB FRACTURE ( 6 FDA reports)
THROMBOSIS ( 6 FDA reports)
TONGUE OEDEMA ( 6 FDA reports)
ULCER ( 6 FDA reports)
UNRESPONSIVE TO STIMULI ( 6 FDA reports)
VIRAL INFECTION ( 6 FDA reports)
ABDOMINAL DISCOMFORT ( 5 FDA reports)
ABDOMINAL DISTENSION ( 5 FDA reports)
ABSCESS BACTERIAL ( 5 FDA reports)
BLOOD BILIRUBIN INCREASED ( 5 FDA reports)
BLOOD CALCIUM INCREASED ( 5 FDA reports)
BLOOD LACTATE DEHYDROGENASE INCREASED ( 5 FDA reports)
BLOOD UREA INCREASED ( 5 FDA reports)
BRONCHOSPASM ( 5 FDA reports)
CARDIAC FAILURE CHRONIC ( 5 FDA reports)
CARDIO-RESPIRATORY ARREST ( 5 FDA reports)
CARDIOVASCULAR INSUFFICIENCY ( 5 FDA reports)
CELLULITIS ( 5 FDA reports)
CEREBRAL INFARCTION ( 5 FDA reports)
CHEST DISCOMFORT ( 5 FDA reports)
CHRONIC OBSTRUCTIVE PULMONARY DISEASE ( 5 FDA reports)
DEPRESSED LEVEL OF CONSCIOUSNESS ( 5 FDA reports)
DERMATITIS ( 5 FDA reports)
DIABETES MELLITUS ( 5 FDA reports)
DRUG ERUPTION ( 5 FDA reports)
DRY SKIN ( 5 FDA reports)
DYSPNOEA AT REST ( 5 FDA reports)
DYSSTASIA ( 5 FDA reports)
EATING DISORDER ( 5 FDA reports)
ELECTROCARDIOGRAM ST SEGMENT DEPRESSION ( 5 FDA reports)
ENCEPHALITIS ( 5 FDA reports)
ERYSIPELOID ( 5 FDA reports)
FACE OEDEMA ( 5 FDA reports)
FEAR ( 5 FDA reports)
FOOT DEFORMITY ( 5 FDA reports)
GASTRIC HAEMORRHAGE ( 5 FDA reports)
GASTROINTESTINAL DISORDER ( 5 FDA reports)
GASTROINTESTINAL VIRAL INFECTION ( 5 FDA reports)
GLYCOSYLATED HAEMOGLOBIN INCREASED ( 5 FDA reports)
HEPATIC ENZYME INCREASED ( 5 FDA reports)
HEPATITIS B DNA INCREASED ( 5 FDA reports)
HEPATOMEGALY ( 5 FDA reports)
HOSPITALISATION ( 5 FDA reports)
HYPERGLYCAEMIA ( 5 FDA reports)
HYPOPHAGIA ( 5 FDA reports)
ILEUS ( 5 FDA reports)
INJECTION SITE ERYTHEMA ( 5 FDA reports)
INTESTINAL ULCER ( 5 FDA reports)
LUNG ADENOCARCINOMA METASTATIC ( 5 FDA reports)
LUNG INFILTRATION ( 5 FDA reports)
MEMORY IMPAIRMENT ( 5 FDA reports)
MENTAL DISORDER ( 5 FDA reports)
MITRAL VALVE INCOMPETENCE ( 5 FDA reports)
MOBILITY DECREASED ( 5 FDA reports)
MULTIPLE MYELOMA ( 5 FDA reports)
MUSCULOSKELETAL CHEST PAIN ( 5 FDA reports)
MUSCULOSKELETAL STIFFNESS ( 5 FDA reports)
NEUROLOGICAL SYMPTOM ( 5 FDA reports)
NEUTROPENIA ( 5 FDA reports)
ODYNOPHAGIA ( 5 FDA reports)
ORAL CANDIDIASIS ( 5 FDA reports)
OSTEOMYELITIS ( 5 FDA reports)
PLEURAL DISORDER ( 5 FDA reports)
POLYNEUROPATHY ( 5 FDA reports)
PULMONARY CONGESTION ( 5 FDA reports)
PULMONARY FIBROSIS ( 5 FDA reports)
PYELONEPHRITIS ( 5 FDA reports)
RENAL CYST ( 5 FDA reports)
RESTLESS LEGS SYNDROME ( 5 FDA reports)
SENSORY LOSS ( 5 FDA reports)
SKIN NECROSIS ( 5 FDA reports)
SKIN ULCER ( 5 FDA reports)
SPINAL DISORDER ( 5 FDA reports)
SUBILEUS ( 5 FDA reports)
SWELLING FACE ( 5 FDA reports)
TRICUSPID VALVE INCOMPETENCE ( 5 FDA reports)
UPPER LIMB FRACTURE ( 5 FDA reports)
VENTRICULAR HYPERTROPHY ( 5 FDA reports)
WHEEZING ( 5 FDA reports)
ABNORMAL BEHAVIOUR ( 4 FDA reports)
ALCOHOL ABUSE ( 4 FDA reports)
ANAL FISTULA ( 4 FDA reports)
ANAPHYLACTIC SHOCK ( 4 FDA reports)
ANGINA PECTORIS ( 4 FDA reports)
ANGIOEDEMA ( 4 FDA reports)
ANKLE FRACTURE ( 4 FDA reports)
AORTIC ARTERIOSCLEROSIS ( 4 FDA reports)
APPENDICITIS ( 4 FDA reports)
AUTOIMMUNE THROMBOCYTOPENIA ( 4 FDA reports)
BALANCE DISORDER ( 4 FDA reports)
BLADDER OBSTRUCTION ( 4 FDA reports)
BLADDER TAMPONADE ( 4 FDA reports)
BLOOD CALCIUM DECREASED ( 4 FDA reports)
BLOOD CREATINE INCREASED ( 4 FDA reports)
BLOOD PHOSPHORUS INCREASED ( 4 FDA reports)
BLOOD PRESSURE DECREASED ( 4 FDA reports)
BONE SWELLING ( 4 FDA reports)
BREAST CANCER ( 4 FDA reports)
BRONCHOPNEUMONIA ( 4 FDA reports)
CARDIOVASCULAR DISORDER ( 4 FDA reports)
CATHETER SITE PAIN ( 4 FDA reports)
CHAPPED LIPS ( 4 FDA reports)
CHOLECYSTITIS ( 4 FDA reports)
COAGULOPATHY ( 4 FDA reports)
COMA ( 4 FDA reports)
CYSTITIS ( 4 FDA reports)
DECUBITUS ULCER ( 4 FDA reports)
DEPRESSED MOOD ( 4 FDA reports)
DEVICE DISLOCATION ( 4 FDA reports)
DIALYSIS ( 4 FDA reports)
DIASTOLIC DYSFUNCTION ( 4 FDA reports)
DISSEMINATED TUBERCULOSIS ( 4 FDA reports)
DRY THROAT ( 4 FDA reports)
DYSARTHRIA ( 4 FDA reports)
ENDOTRACHEAL INTUBATION ( 4 FDA reports)
EPISTAXIS ( 4 FDA reports)
EYE PAIN ( 4 FDA reports)
FAECES DISCOLOURED ( 4 FDA reports)
FIBRIN D DIMER INCREASED ( 4 FDA reports)
FISTULA ( 4 FDA reports)
GLOMERULAR FILTRATION RATE DECREASED ( 4 FDA reports)
HAEMOLYTIC ANAEMIA ( 4 FDA reports)
HAEMORRHAGIC DIATHESIS ( 4 FDA reports)
HEART RATE DECREASED ( 4 FDA reports)
HEART RATE INCREASED ( 4 FDA reports)
HEPATIC CIRRHOSIS ( 4 FDA reports)
HEPATITIS B ( 4 FDA reports)
HERNIA ( 4 FDA reports)
HIP FRACTURE ( 4 FDA reports)
HYDRONEPHROSIS ( 4 FDA reports)
HYPERCALCAEMIA ( 4 FDA reports)
HYPERPARATHYROIDISM SECONDARY ( 4 FDA reports)
HYPERTENSIVE NEPHROPATHY ( 4 FDA reports)
INJECTION SITE PAIN ( 4 FDA reports)
INJECTION SITE REACTION ( 4 FDA reports)
INTENTIONAL OVERDOSE ( 4 FDA reports)
JOINT ANKYLOSIS ( 4 FDA reports)
JOINT INJURY ( 4 FDA reports)
LEFT ATRIAL DILATATION ( 4 FDA reports)
LIMB DISCOMFORT ( 4 FDA reports)
LIMB INJURY ( 4 FDA reports)
MALIGNANT MELANOMA ( 4 FDA reports)
METABOLIC ACIDOSIS ( 4 FDA reports)
MOTOR DYSFUNCTION ( 4 FDA reports)
MOUTH ULCERATION ( 4 FDA reports)
NAIL DISORDER ( 4 FDA reports)
NOCTURIA ( 4 FDA reports)
OFF LABEL USE ( 4 FDA reports)
OROPHARYNGEAL PAIN ( 4 FDA reports)
OSTEONECROSIS OF JAW ( 4 FDA reports)
OVERDOSE ( 4 FDA reports)
PENILE OEDEMA ( 4 FDA reports)
PERFORMANCE STATUS DECREASED ( 4 FDA reports)
PERIANAL ABSCESS ( 4 FDA reports)
PNEUMOCYSTIS JIROVECI PNEUMONIA ( 4 FDA reports)
POSTOPERATIVE THROMBOSIS ( 4 FDA reports)
POSTRENAL FAILURE ( 4 FDA reports)
PREGNANCY ( 4 FDA reports)
PROCTITIS ( 4 FDA reports)
PROSTATIC OPERATION ( 4 FDA reports)
PROTEINURIA ( 4 FDA reports)
RASH MACULAR ( 4 FDA reports)
RASH PUSTULAR ( 4 FDA reports)
RENAL SURGERY ( 4 FDA reports)
RENAL TUBULAR DISORDER ( 4 FDA reports)
RESPIRATORY TRACT INFECTION ( 4 FDA reports)
RETICULOCYTE COUNT DECREASED ( 4 FDA reports)
RETINOPATHY HYPERTENSIVE ( 4 FDA reports)
RHABDOMYOLYSIS ( 4 FDA reports)
SCROTAL OEDEMA ( 4 FDA reports)
SHOCK ( 4 FDA reports)
SKIN INDURATION ( 4 FDA reports)
SPINAL COLUMN STENOSIS ( 4 FDA reports)
SPINAL FRACTURE ( 4 FDA reports)
STOMATITIS ( 4 FDA reports)
SYNOVECTOMY ( 4 FDA reports)
TACHYPNOEA ( 4 FDA reports)
TENDONITIS ( 4 FDA reports)
TETANY ( 4 FDA reports)
THROAT TIGHTNESS ( 4 FDA reports)
UPPER RESPIRATORY TRACT INFECTION ( 4 FDA reports)
URINARY BLADDER HAEMORRHAGE ( 4 FDA reports)
UROSEPSIS ( 4 FDA reports)
VARICES OESOPHAGEAL ( 4 FDA reports)
VASCULAR DEMENTIA ( 4 FDA reports)
VISUAL ACUITY REDUCED ( 4 FDA reports)
ABORTION SPONTANEOUS ( 3 FDA reports)
ABSCESS ( 3 FDA reports)
ACUTE MYOCARDIAL INFARCTION ( 3 FDA reports)
ALVEOLITIS FIBROSING ( 3 FDA reports)
ANOREXIA ( 3 FDA reports)
APNOEA ( 3 FDA reports)
APRAXIA ( 3 FDA reports)
ARTHROPATHY ( 3 FDA reports)
ASPHYXIA ( 3 FDA reports)
BACTERIAL INFECTION ( 3 FDA reports)
BENIGN PROSTATIC HYPERPLASIA ( 3 FDA reports)
BLEPHAROSPASM ( 3 FDA reports)
BLISTER ( 3 FDA reports)
BUNDLE BRANCH BLOCK ( 3 FDA reports)
CARDIOACTIVE DRUG LEVEL INCREASED ( 3 FDA reports)
CARPAL TUNNEL SYNDROME ( 3 FDA reports)
CATARACT ( 3 FDA reports)
CHRONIC HEPATITIS ( 3 FDA reports)
CLOSTRIDIUM DIFFICILE COLITIS ( 3 FDA reports)
COLON ADENOMA ( 3 FDA reports)
CONTUSION ( 3 FDA reports)
COR PULMONALE ( 3 FDA reports)
COSTOCHONDRITIS ( 3 FDA reports)
CRYING ( 3 FDA reports)
CYST ( 3 FDA reports)
DEFAECATION URGENCY ( 3 FDA reports)
DELIRIUM ( 3 FDA reports)
DEMENTIA ( 3 FDA reports)
DEMYELINATION ( 3 FDA reports)
DEVICE RELATED INFECTION ( 3 FDA reports)
DIFFUSE ALVEOLAR DAMAGE ( 3 FDA reports)
DISEASE RECURRENCE ( 3 FDA reports)
DISSOCIATIVE AMNESIA ( 3 FDA reports)
DIVERTICULITIS ( 3 FDA reports)
DRUG TOXICITY ( 3 FDA reports)
DRY MOUTH ( 3 FDA reports)
DUODENITIS ( 3 FDA reports)
ECCHYMOSIS ( 3 FDA reports)
ENDOCARDITIS BACTERIAL ( 3 FDA reports)
EXCORIATION ( 3 FDA reports)
EXTRADURAL HAEMATOMA ( 3 FDA reports)
EYE IRRITATION ( 3 FDA reports)
EYE SWELLING ( 3 FDA reports)
EYELID OEDEMA ( 3 FDA reports)
FEMUR FRACTURE ( 3 FDA reports)
FIBROMYALGIA ( 3 FDA reports)
FISTULA REPAIR ( 3 FDA reports)
FLATULENCE ( 3 FDA reports)
GLAUCOMA ( 3 FDA reports)
GOUT ( 3 FDA reports)
GROIN PAIN ( 3 FDA reports)
HAEMORRHAGIC ANAEMIA ( 3 FDA reports)
HAEMORRHOIDS ( 3 FDA reports)
HEMIPARESIS ( 3 FDA reports)
HEPATIC FAILURE ( 3 FDA reports)
HEPATIC NEOPLASM MALIGNANT ( 3 FDA reports)
HEPATOTOXICITY ( 3 FDA reports)
HYPERCHOLESTEROLAEMIA ( 3 FDA reports)
HYPERSOMNIA ( 3 FDA reports)
HYPERTRIGLYCERIDAEMIA ( 3 FDA reports)
HYPOALBUMINAEMIA ( 3 FDA reports)
HYPOXIC-ISCHAEMIC ENCEPHALOPATHY ( 3 FDA reports)
ILL-DEFINED DISORDER ( 3 FDA reports)
INFLAMMATORY MARKER INCREASED ( 3 FDA reports)
INFLUENZA ( 3 FDA reports)
INJURY ( 3 FDA reports)
INTERVERTEBRAL DISC DEGENERATION ( 3 FDA reports)
INTERVERTEBRAL DISC OPERATION ( 3 FDA reports)
INTESTINAL INFARCTION ( 3 FDA reports)
INTESTINAL STENOSIS ( 3 FDA reports)
ISCHAEMIC STROKE ( 3 FDA reports)
JAUNDICE ( 3 FDA reports)
JOINT DISLOCATION ( 3 FDA reports)
LACRIMATION INCREASED ( 3 FDA reports)
LEFT VENTRICULAR HYPERTROPHY ( 3 FDA reports)
LOWER LIMB FRACTURE ( 3 FDA reports)
LUMBAR SPINAL STENOSIS ( 3 FDA reports)
LUNG DISORDER ( 3 FDA reports)
LUPUS-LIKE SYNDROME ( 3 FDA reports)
LYMPH NODE CALCIFICATION ( 3 FDA reports)
LYMPHADENITIS ( 3 FDA reports)
MALNUTRITION ( 3 FDA reports)
MATERNAL EXPOSURE DURING PREGNANCY ( 3 FDA reports)
MENINGITIS ASEPTIC ( 3 FDA reports)
MENTAL DISORDER DUE TO A GENERAL MEDICAL CONDITION ( 3 FDA reports)
MIXED CONNECTIVE TISSUE DISEASE ( 3 FDA reports)
MONOPLEGIA ( 3 FDA reports)
MUCOSAL INFLAMMATION ( 3 FDA reports)
MULTI-ORGAN FAILURE ( 3 FDA reports)
MUSCLE INJURY ( 3 FDA reports)
MYELITIS ( 3 FDA reports)
NECK MASS ( 3 FDA reports)
NECROSIS ( 3 FDA reports)
NEGATIVE THOUGHTS ( 3 FDA reports)
NEURALGIA ( 3 FDA reports)
NODULE ( 3 FDA reports)
NON-HODGKIN'S LYMPHOMA ( 3 FDA reports)
OESOPHAGEAL HYPOMOTILITY ( 3 FDA reports)
OESOPHAGEAL STENOSIS ( 3 FDA reports)
OPTIC NEURITIS ( 3 FDA reports)
OSTEOPOROSIS ( 3 FDA reports)
OXYGEN SATURATION DECREASED ( 3 FDA reports)
PARAPLEGIA ( 3 FDA reports)
PERIPHERAL ISCHAEMIA ( 3 FDA reports)
PETECHIAE ( 3 FDA reports)
POOR QUALITY DRUG ADMINISTERED ( 3 FDA reports)
PREMATURE DELIVERY ( 3 FDA reports)
PULMONARY ARTERIAL HYPERTENSION ( 3 FDA reports)
PULMONARY TUBERCULOSIS ( 3 FDA reports)
PULSELESS ELECTRICAL ACTIVITY ( 3 FDA reports)
RADIOACTIVE IODINE THERAPY ( 3 FDA reports)
RASH ERYTHEMATOUS ( 3 FDA reports)
RECTAL TENESMUS ( 3 FDA reports)
RED BLOOD CELL SEDIMENTATION RATE INCREASED ( 3 FDA reports)
RHEUMATOID NODULE ( 3 FDA reports)
SCIATICA ( 3 FDA reports)
SELF-MEDICATION ( 3 FDA reports)
SEPTIC SHOCK ( 3 FDA reports)
SPINAL OPERATION ( 3 FDA reports)
STEVENS-JOHNSON SYNDROME ( 3 FDA reports)
STUPOR ( 3 FDA reports)
SUBCUTANEOUS ABSCESS ( 3 FDA reports)
THINKING ABNORMAL ( 3 FDA reports)
THORACIC VERTEBRAL FRACTURE ( 3 FDA reports)
THYROTOXIC CRISIS ( 3 FDA reports)
TIBIA FRACTURE ( 3 FDA reports)
TONGUE DRY ( 3 FDA reports)
TOXIC EPIDERMAL NECROLYSIS ( 3 FDA reports)
TRANSAMINASES INCREASED ( 3 FDA reports)
TROPONIN INCREASED ( 3 FDA reports)
URINARY INCONTINENCE ( 3 FDA reports)
VAGINAL HAEMORRHAGE ( 3 FDA reports)
VENOUS THROMBOSIS LIMB ( 3 FDA reports)
VENTRICULAR EXTRASYSTOLES ( 3 FDA reports)
VENTRICULAR FIBRILLATION ( 3 FDA reports)
WOUND ( 3 FDA reports)
ABDOMINAL INJURY ( 2 FDA reports)
ABDOMINAL MASS ( 2 FDA reports)
ABSCESS LIMB ( 2 FDA reports)
ACCIDENTAL OVERDOSE ( 2 FDA reports)
ACTIVATED PARTIAL THROMBOPLASTIN TIME PROLONGED ( 2 FDA reports)
ACUTE MYELOID LEUKAEMIA ( 2 FDA reports)
ADENOSINE DEAMINASE DEFICIENCY ( 2 FDA reports)
AFFECTIVE DISORDER ( 2 FDA reports)
AGITATED DEPRESSION ( 2 FDA reports)
ALTERED STATE OF CONSCIOUSNESS ( 2 FDA reports)
ANGER ( 2 FDA reports)
ANTINUCLEAR ANTIBODY POSITIVE ( 2 FDA reports)
ANTIPHOSPHOLIPID ANTIBODIES ( 2 FDA reports)
ANTIPSYCHOTIC DRUG LEVEL INCREASED ( 2 FDA reports)
AORTITIS ( 2 FDA reports)
APATHY ( 2 FDA reports)
APHONIA ( 2 FDA reports)
ARTERIOSCLEROSIS CORONARY ARTERY ( 2 FDA reports)
ARTHRITIS BACTERIAL ( 2 FDA reports)
ARTHRODESIS ( 2 FDA reports)
ASPIRATION ( 2 FDA reports)
ATRIAL FLUTTER ( 2 FDA reports)
BACK DISORDER ( 2 FDA reports)
BARTHOLIN'S ABSCESS ( 2 FDA reports)
BASAL CELL CARCINOMA ( 2 FDA reports)
BEHCET'S SYNDROME ( 2 FDA reports)
BLADDER PROLAPSE ( 2 FDA reports)
BLEPHARITIS ( 2 FDA reports)
BLOOD BILIRUBIN ABNORMAL ( 2 FDA reports)
BLOOD CREATININE DECREASED ( 2 FDA reports)
BLOOD POTASSIUM DECREASED ( 2 FDA reports)
BLOOD PRESSURE SYSTOLIC INCREASED ( 2 FDA reports)
BLOOD PROLACTIN INCREASED ( 2 FDA reports)
BONE MARROW DISORDER ( 2 FDA reports)
BONE NEOPLASM MALIGNANT ( 2 FDA reports)
BRACHIAL PLEXUS INJURY ( 2 FDA reports)
BREAST ABSCESS ( 2 FDA reports)
BREAST CANCER FEMALE ( 2 FDA reports)
BRONCHITIS ( 2 FDA reports)
BURSITIS ( 2 FDA reports)
CANDIDIASIS ( 2 FDA reports)
CARDIAC FAILURE CONGESTIVE ( 2 FDA reports)
CENTRAL NERVOUS SYSTEM LESION ( 2 FDA reports)
CEREBRAL MICROANGIOPATHY ( 2 FDA reports)
CERVICAL SPINE FLATTENING ( 2 FDA reports)
CHEILITIS GRANULOMATOSA ( 2 FDA reports)
CHEST X-RAY ABNORMAL ( 2 FDA reports)
CHOLECYSTECTOMY ( 2 FDA reports)
CHRONIC FATIGUE SYNDROME ( 2 FDA reports)
COAGULATION TEST ABNORMAL ( 2 FDA reports)
COLD SWEAT ( 2 FDA reports)
COOMBS POSITIVE HAEMOLYTIC ANAEMIA ( 2 FDA reports)
COORDINATION ABNORMAL ( 2 FDA reports)
CORONARY ARTERY THROMBOSIS ( 2 FDA reports)
DELUSION ( 2 FDA reports)
DENTAL IMPLANTATION ( 2 FDA reports)
DENTAL OPERATION ( 2 FDA reports)
DERMAL CYST ( 2 FDA reports)
DIABETIC FOOT ( 2 FDA reports)
DIABETIC NEUROPATHY ( 2 FDA reports)
DIARRHOEA HAEMORRHAGIC ( 2 FDA reports)
DILATATION ATRIAL ( 2 FDA reports)
DISEASE PROGRESSION ( 2 FDA reports)
DISTURBANCE IN SEXUAL AROUSAL ( 2 FDA reports)
DIVERTICULUM INTESTINAL ( 2 FDA reports)
DRUG ABUSER ( 2 FDA reports)
DRUG DISPENSING ERROR ( 2 FDA reports)
DRUG LEVEL INCREASED ( 2 FDA reports)
DRY EYE ( 2 FDA reports)
DYSHIDROSIS ( 2 FDA reports)
DYSPHONIA ( 2 FDA reports)
EAR INFECTION ( 2 FDA reports)
EAR PAIN ( 2 FDA reports)
ELECTROCARDIOGRAM QT PROLONGED ( 2 FDA reports)
ELECTROCARDIOGRAM REPOLARISATION ABNORMALITY ( 2 FDA reports)
EMPHYSEMA ( 2 FDA reports)
EMPYEMA ( 2 FDA reports)
ENCEPHALITIS VIRAL ( 2 FDA reports)
ENTEROCOLITIS HAEMORRHAGIC ( 2 FDA reports)
ENTEROCUTANEOUS FISTULA ( 2 FDA reports)
EPILEPSY ( 2 FDA reports)
EPSTEIN-BARR VIRUS INFECTION ( 2 FDA reports)
ERYTHEMA OF EYELID ( 2 FDA reports)
EXECUTIVE DYSFUNCTION ( 2 FDA reports)
EYE INFLAMMATION ( 2 FDA reports)
FACIAL PARESIS ( 2 FDA reports)
FEELING HOT ( 2 FDA reports)
FIBULA FRACTURE ( 2 FDA reports)
FLANK PAIN ( 2 FDA reports)
FOOT FRACTURE ( 2 FDA reports)
FOOT OPERATION ( 2 FDA reports)
FOREARM FRACTURE ( 2 FDA reports)
FURUNCLE ( 2 FDA reports)
GALLBLADDER DISORDER ( 2 FDA reports)
GALLBLADDER OPERATION ( 2 FDA reports)
GASTRIC INFECTION ( 2 FDA reports)
GASTROENTERITIS ( 2 FDA reports)
GASTROENTERITIS NOROVIRUS ( 2 FDA reports)
GASTROINTESTINAL ANASTOMOTIC LEAK ( 2 FDA reports)
GASTROINTESTINAL EROSION ( 2 FDA reports)
GASTROINTESTINAL ULCER PERFORATION ( 2 FDA reports)
GENE MUTATION ( 2 FDA reports)
GINGIVAL SWELLING ( 2 FDA reports)
GLOSSODYNIA ( 2 FDA reports)
GOITRE ( 2 FDA reports)
GRAND MAL CONVULSION ( 2 FDA reports)
HAEMANGIOMA OF LIVER ( 2 FDA reports)
HAEMATOCHEZIA ( 2 FDA reports)
HAEMATOSPERMIA ( 2 FDA reports)
HAEMODYNAMIC INSTABILITY ( 2 FDA reports)
HAEMORRHAGE ( 2 FDA reports)
HALLUCINATION, AUDITORY ( 2 FDA reports)
HEART RATE IRREGULAR ( 2 FDA reports)
HEMIPLEGIA ( 2 FDA reports)
HEPATIC NECROSIS ( 2 FDA reports)
HEPATIC NEOPLASM ( 2 FDA reports)
HEPATORENAL SYNDROME ( 2 FDA reports)
HIP ARTHROPLASTY ( 2 FDA reports)
HORDEOLUM ( 2 FDA reports)
HUMERUS FRACTURE ( 2 FDA reports)
HYDROTHORAX ( 2 FDA reports)
HYPERKALAEMIA ( 2 FDA reports)
HYPERTENSIVE CRISIS ( 2 FDA reports)
HYPOAESTHESIA FACIAL ( 2 FDA reports)
IDIOPATHIC THROMBOCYTOPENIC PURPURA ( 2 FDA reports)
IMMOBILE ( 2 FDA reports)
IMMUNOSUPPRESSION ( 2 FDA reports)
INCREASED APPETITE ( 2 FDA reports)
INTERSTITIAL LUNG DISEASE ( 2 FDA reports)
INTESTINAL OBSTRUCTION ( 2 FDA reports)
IRITIS ( 2 FDA reports)
JAUNDICE CHOLESTATIC ( 2 FDA reports)
JAW OPERATION ( 2 FDA reports)
JOINT DESTRUCTION ( 2 FDA reports)
KNEE OPERATION ( 2 FDA reports)
LARGE INTESTINAL ULCER ( 2 FDA reports)
LATENT TUBERCULOSIS ( 2 FDA reports)
LIGAMENT LAXITY ( 2 FDA reports)
LIMB DEFORMITY ( 2 FDA reports)
LIVER ABSCESS ( 2 FDA reports)
LOGORRHOEA ( 2 FDA reports)
LUMBAR VERTEBRAL FRACTURE ( 2 FDA reports)
LUNG CONSOLIDATION ( 2 FDA reports)
LUNG INFECTION ( 2 FDA reports)
LYMPH NODE TUBERCULOSIS ( 2 FDA reports)
MANIA ( 2 FDA reports)
MASTICATION DISORDER ( 2 FDA reports)
MASTITIS ( 2 FDA reports)
MENINGITIS ( 2 FDA reports)
MENTAL STATUS CHANGES ( 2 FDA reports)
METASTASES TO SPINE ( 2 FDA reports)
METASTATIC MALIGNANT MELANOMA ( 2 FDA reports)
MICROCYTIC ANAEMIA ( 2 FDA reports)
MICTURITION URGENCY ( 2 FDA reports)
MOUTH HAEMORRHAGE ( 2 FDA reports)
MULTIMORBIDITY ( 2 FDA reports)
MULTIPLE DRUG OVERDOSE INTENTIONAL ( 2 FDA reports)
MUSCLE DISORDER ( 2 FDA reports)
MUSCULOSKELETAL DISORDER ( 2 FDA reports)
MYOCARDITIS ( 2 FDA reports)
NASAL CONGESTION ( 2 FDA reports)
NECROSIS ISCHAEMIC ( 2 FDA reports)
NERVE COMPRESSION ( 2 FDA reports)
NERVOUSNESS ( 2 FDA reports)
NEUROPATHY PERIPHERAL ( 2 FDA reports)
NIGHTMARE ( 2 FDA reports)
NO THERAPEUTIC RESPONSE ( 2 FDA reports)
NON-CARDIAC CHEST PAIN ( 2 FDA reports)
OBSTRUCTION GASTRIC ( 2 FDA reports)
OCCULT BLOOD ( 2 FDA reports)
OEDEMA MOUTH ( 2 FDA reports)
OESOPHAGITIS ( 2 FDA reports)
OSTEITIS ( 2 FDA reports)
OSTEOMYELITIS CHRONIC ( 2 FDA reports)
OSTEOPENIA ( 2 FDA reports)
OVARIAN CANCER ( 2 FDA reports)
OVARIAN NEOPLASM ( 2 FDA reports)
PALATAL OEDEMA ( 2 FDA reports)
PALMAR-PLANTAR ERYTHRODYSAESTHESIA SYNDROME ( 2 FDA reports)
PANCREATIC CARCINOMA METASTATIC ( 2 FDA reports)
PANCREATOLITHIASIS ( 2 FDA reports)
PARKINSON'S DISEASE ( 2 FDA reports)
PAROSMIA ( 2 FDA reports)
PAROTID GLAND ENLARGEMENT ( 2 FDA reports)
PERICARDIAL EFFUSION ( 2 FDA reports)
PERICARDITIS ( 2 FDA reports)
PERIPHERAL ARTERIAL OCCLUSIVE DISEASE ( 2 FDA reports)
PERIPHERAL VASCULAR DISORDER ( 2 FDA reports)
PERSONALITY CHANGE ( 2 FDA reports)
PHOTOSENSITIVITY REACTION ( 2 FDA reports)
POLYDIPSIA ( 2 FDA reports)
POSTOPERATIVE WOUND COMPLICATION ( 2 FDA reports)
PREMATURE BABY ( 2 FDA reports)
PROCEDURAL COMPLICATION ( 2 FDA reports)
PSEUDOMEMBRANOUS COLITIS ( 2 FDA reports)
PSYCHOMOTOR HYPERACTIVITY ( 2 FDA reports)
PULMONARY ARTERY THROMBOSIS ( 2 FDA reports)
PULMONARY HYPERTENSION ( 2 FDA reports)
PUSTULAR PSORIASIS ( 2 FDA reports)
RADICULAR PAIN ( 2 FDA reports)
RADIUS FRACTURE ( 2 FDA reports)
RALES ( 2 FDA reports)
RASH MACULO-PAPULAR ( 2 FDA reports)
RECTAL CANCER ( 2 FDA reports)
RENAL DISORDER ( 2 FDA reports)
RENAL TUBULAR NECROSIS ( 2 FDA reports)
RESPIRATORY ARREST ( 2 FDA reports)
RESPIRATORY DISORDER ( 2 FDA reports)
ROTATOR CUFF SYNDROME ( 2 FDA reports)
SALIVARY GLAND CALCULUS ( 2 FDA reports)
SEMINOMA ( 2 FDA reports)
SEPTIC ARTHRITIS STAPHYLOCOCCAL ( 2 FDA reports)
SJOGREN'S SYNDROME ( 2 FDA reports)
SKIN DISCOLOURATION ( 2 FDA reports)
SKIN HAEMORRHAGE ( 2 FDA reports)
SKIN LACERATION ( 2 FDA reports)
SLUGGISHNESS ( 2 FDA reports)
SMALL FOR DATES BABY ( 2 FDA reports)
SPHINCTER OF ODDI DYSFUNCTION ( 2 FDA reports)
SPINAL COLUMN INJURY ( 2 FDA reports)
SPINAL LAMINECTOMY ( 2 FDA reports)
SPINAL OSTEOARTHRITIS ( 2 FDA reports)
SPLENIC RUPTURE ( 2 FDA reports)
STAPHYLOCOCCAL SEPSIS ( 2 FDA reports)
SUBARACHNOID HAEMORRHAGE ( 2 FDA reports)
SUBDURAL HAEMATOMA ( 2 FDA reports)
SUBMANDIBULAR MASS ( 2 FDA reports)
SUNBURN ( 2 FDA reports)
SURGERY ( 2 FDA reports)
SWOLLEN TONGUE ( 2 FDA reports)
SYNOVIAL CYST ( 2 FDA reports)
SYPHILIS ( 2 FDA reports)
TENDERNESS ( 2 FDA reports)
THERAPEUTIC RESPONSE UNEXPECTED ( 2 FDA reports)
THROMBOPHLEBITIS ( 2 FDA reports)
THYROID CANCER ( 2 FDA reports)
THYROID CANCER RECURRENT ( 2 FDA reports)
TINNITUS ( 2 FDA reports)
TONGUE PARALYSIS ( 2 FDA reports)
TOOTH AVULSION ( 2 FDA reports)
TOOTH LOSS ( 2 FDA reports)
TRANSIENT ISCHAEMIC ATTACK ( 2 FDA reports)
TRAUMATIC BRAIN INJURY ( 2 FDA reports)
TREATMENT FAILURE ( 2 FDA reports)
TYPE 2 DIABETES MELLITUS ( 2 FDA reports)
UMBILICAL HERNIA ( 2 FDA reports)
VAGINAL INFECTION ( 2 FDA reports)
VASCULAR CALCIFICATION ( 2 FDA reports)
VASCULAR INSUFFICIENCY ( 2 FDA reports)
VENOUS THROMBOSIS ( 2 FDA reports)
VENTRICULAR DYSFUNCTION ( 2 FDA reports)
VIRAL TEST NEGATIVE ( 2 FDA reports)
WEGENER'S GRANULOMATOSIS ( 2 FDA reports)
WHITE BLOOD CELL COUNT DECREASED ( 2 FDA reports)
WHITE BLOOD CELL COUNT INCREASED ( 2 FDA reports)
WOUND COMPLICATION ( 2 FDA reports)
WOUND SECRETION ( 2 FDA reports)
WOUND TREATMENT ( 2 FDA reports)
ABDOMINAL ADHESIONS ( 1 FDA reports)
ABDOMINAL HERNIA ( 1 FDA reports)
ABDOMINAL PAIN LOWER ( 1 FDA reports)
ABDOMINAL REBOUND TENDERNESS ( 1 FDA reports)
ABNORMAL DREAMS ( 1 FDA reports)
ABNORMAL SENSATION IN EYE ( 1 FDA reports)
ABORTION ( 1 FDA reports)
ABSCESS DRAINAGE ( 1 FDA reports)
ABSCESS INTESTINAL ( 1 FDA reports)
ACCIDENT ( 1 FDA reports)
ACIDOSIS ( 1 FDA reports)
ACNE ( 1 FDA reports)
ACQUIRED CLAW TOE ( 1 FDA reports)
ACTIVATED PARTIAL THROMBOPLASTIN TIME SHORTENED ( 1 FDA reports)
ACUTE CORONARY SYNDROME ( 1 FDA reports)
ACUTE ENDOCARDITIS ( 1 FDA reports)
ADVERSE DRUG REACTION ( 1 FDA reports)
AGRANULOCYTOSIS ( 1 FDA reports)
ALCOHOL WITHDRAWAL SYNDROME ( 1 FDA reports)
ALLERGIC GRANULOMATOUS ANGIITIS ( 1 FDA reports)
ALOPECIA TOTALIS ( 1 FDA reports)
ALOPECIA UNIVERSALIS ( 1 FDA reports)
ALVEOLITIS ALLERGIC ( 1 FDA reports)
AMYOTROPHIC LATERAL SCLEROSIS ( 1 FDA reports)
ANAEMIA POSTOPERATIVE ( 1 FDA reports)
ANAL ATRESIA ( 1 FDA reports)
ANAL CANCER ( 1 FDA reports)
ANAL FISSURE ( 1 FDA reports)
ANAL HAEMORRHAGE ( 1 FDA reports)
ANAL INFECTION ( 1 FDA reports)
ANDROGENETIC ALOPECIA ( 1 FDA reports)
ANGIOIMMUNOBLASTIC T-CELL LYMPHOMA STAGE III ( 1 FDA reports)
ANORECTAL VARICES ( 1 FDA reports)
ANTICHOLINERGIC SYNDROME ( 1 FDA reports)
ANTIPHOSPHOLIPID ANTIBODIES POSITIVE ( 1 FDA reports)
ANTIPHOSPHOLIPID SYNDROME ( 1 FDA reports)
ANURIA ( 1 FDA reports)
AORTIC CALCIFICATION ( 1 FDA reports)
AORTIC STENOSIS ( 1 FDA reports)
APPENDICECTOMY ( 1 FDA reports)
ARTERIOSCLEROSIS ( 1 FDA reports)
ARTHRITIS INFECTIVE ( 1 FDA reports)
ARTHRITIS REACTIVE ( 1 FDA reports)
ASPERGILLUS TEST POSITIVE ( 1 FDA reports)
ATRIAL SEPTAL DEFECT ( 1 FDA reports)
AUTOIMMUNE DISORDER ( 1 FDA reports)
B-CELL LYMPHOMA ( 1 FDA reports)
BACTERIAL TEST ( 1 FDA reports)
BENIGN NEOPLASM ( 1 FDA reports)
BENIGN NEOPLASM OF SKIN ( 1 FDA reports)
BIOPSY SITE UNSPECIFIED ABNORMAL ( 1 FDA reports)
BLADDER CATHETERISATION ( 1 FDA reports)
BLADDER DISORDER ( 1 FDA reports)
BLINDNESS ( 1 FDA reports)
BLOOD AMYLASE INCREASED ( 1 FDA reports)
BLOOD CREATINE PHOSPHOKINASE MB ( 1 FDA reports)
BLOOD GLUCOSE DECREASED ( 1 FDA reports)
BLOOD POTASSIUM INCREASED ( 1 FDA reports)
BLOOD SODIUM DECREASED ( 1 FDA reports)
BLOOD THYROID STIMULATING HORMONE ABNORMAL ( 1 FDA reports)
BLOODY DISCHARGE ( 1 FDA reports)
BONE EROSION ( 1 FDA reports)
BONE FORMATION DECREASED ( 1 FDA reports)
BONE MARROW DEPRESSION ( 1 FDA reports)
BONE MARROW FAILURE ( 1 FDA reports)
BONE TUBERCULOSIS ( 1 FDA reports)
BORDERLINE OVARIAN TUMOUR ( 1 FDA reports)
BOWEN'S DISEASE ( 1 FDA reports)
BRADYPHRENIA ( 1 FDA reports)
BREAST DISCHARGE ( 1 FDA reports)
BREAST DISORDER ( 1 FDA reports)
BREATH ODOUR ( 1 FDA reports)
BRONCHIAL DISORDER ( 1 FDA reports)
BRONCHIECTASIS ( 1 FDA reports)
BRONCHIOLOALVEOLAR CARCINOMA ( 1 FDA reports)
BRONCHITIS CHRONIC ( 1 FDA reports)
BRONCHOSCOPY ( 1 FDA reports)
BULLOUS LUNG DISEASE ( 1 FDA reports)
BUNDLE BRANCH BLOCK LEFT ( 1 FDA reports)
BUNION ( 1 FDA reports)
CANDIDA TEST POSITIVE ( 1 FDA reports)
CARDIAC ABLATION ( 1 FDA reports)
CARDIAC FAILURE ACUTE ( 1 FDA reports)
CARDIAC PACEMAKER INSERTION ( 1 FDA reports)
CARDIAC VALVE DISEASE ( 1 FDA reports)
CARDIOGENIC SHOCK ( 1 FDA reports)
CARDIOMEGALY ( 1 FDA reports)
CAROTID ARTERY DISSECTION ( 1 FDA reports)
CATARACT OPERATION ( 1 FDA reports)
CATHETER PLACEMENT ( 1 FDA reports)
CEREBRAL ISCHAEMIA ( 1 FDA reports)
CERVICAL DYSPLASIA ( 1 FDA reports)
CERVIX CARCINOMA ( 1 FDA reports)
CHOLANGITIS ( 1 FDA reports)
CLOSTRIDIUM COLITIS ( 1 FDA reports)
CLOSTRIDIUM TEST POSITIVE ( 1 FDA reports)
COLECTOMY ( 1 FDA reports)
COLITIS ISCHAEMIC ( 1 FDA reports)
COLITIS ULCERATIVE ( 1 FDA reports)
COLLAGEN DISORDER ( 1 FDA reports)
COLLAPSE OF LUNG ( 1 FDA reports)
COMPLETED SUICIDE ( 1 FDA reports)
CONCOMITANT DISEASE AGGRAVATED ( 1 FDA reports)
CONJUNCTIVITIS ( 1 FDA reports)
CONNECTIVE TISSUE DISORDER ( 1 FDA reports)
CORONARY ARTERY STENOSIS ( 1 FDA reports)
CREATININE RENAL CLEARANCE DECREASED ( 1 FDA reports)
CYTOMEGALOVIRUS INFECTION ( 1 FDA reports)
DACRYOSTENOSIS ACQUIRED ( 1 FDA reports)
DEAFNESS ( 1 FDA reports)
DEAFNESS NEUROSENSORY ( 1 FDA reports)
DEMYELINATING POLYNEUROPATHY ( 1 FDA reports)
DERMATITIS ALLERGIC ( 1 FDA reports)
DERMATITIS BULLOUS ( 1 FDA reports)
DERMATITIS EXFOLIATIVE ( 1 FDA reports)
DILATATION INTRAHEPATIC DUCT ACQUIRED ( 1 FDA reports)
DIVERTICULUM ( 1 FDA reports)
DRUG DEPENDENCE ( 1 FDA reports)
DRUG EXPOSURE BEFORE PREGNANCY ( 1 FDA reports)
DRUG SPECIFIC ANTIBODY PRESENT ( 1 FDA reports)
DRUG WITHDRAWAL SYNDROME ( 1 FDA reports)
DUODENAL ULCER HAEMORRHAGE ( 1 FDA reports)
DUODENAL ULCER PERFORATION ( 1 FDA reports)
DUPUYTREN'S CONTRACTURE ( 1 FDA reports)
DYSKINESIA ( 1 FDA reports)
DYSLIPIDAEMIA ( 1 FDA reports)
DYSTONIA ( 1 FDA reports)
DYSURIA ( 1 FDA reports)
ELECTROCARDIOGRAM ABNORMAL ( 1 FDA reports)
ELECTROCARDIOGRAM POOR R-WAVE PROGRESSION ( 1 FDA reports)
ELECTROCARDIOGRAM Q WAVE ABNORMAL ( 1 FDA reports)
ELECTROCARDIOGRAM ST SEGMENT ELEVATION ( 1 FDA reports)
EMBOLIC STROKE ( 1 FDA reports)
EMOTIONAL DISORDER ( 1 FDA reports)
ENAMEL ANOMALY ( 1 FDA reports)
ENCEPHALITIS BRAIN STEM ( 1 FDA reports)
ENTEROVESICAL FISTULA ( 1 FDA reports)
EOSINOPHILIC CYSTITIS ( 1 FDA reports)
EPIGASTRIC DISCOMFORT ( 1 FDA reports)
ERECTILE DYSFUNCTION ( 1 FDA reports)
ERYTHEMA INDURATUM ( 1 FDA reports)
ERYTHEMA MULTIFORME ( 1 FDA reports)
ERYTHEMA NODOSUM ( 1 FDA reports)
EUPHORIC MOOD ( 1 FDA reports)
EXOSTOSIS ( 1 FDA reports)
EXPOSURE VIA SEMEN ( 1 FDA reports)
EXTRAPYRAMIDAL DISORDER ( 1 FDA reports)
EYE PRURITUS ( 1 FDA reports)
EYELID OPERATION ( 1 FDA reports)
FACET JOINT SYNDROME ( 1 FDA reports)
FASCIITIS ( 1 FDA reports)
FEBRILE INFECTION ( 1 FDA reports)
FEELING COLD ( 1 FDA reports)
FEELING DRUNK ( 1 FDA reports)
FEMALE GENITAL TRACT FISTULA ( 1 FDA reports)
FIBROCYSTIC BREAST DISEASE ( 1 FDA reports)
FISTULA DISCHARGE ( 1 FDA reports)
FLUID RETENTION ( 1 FDA reports)
FOCAL NODULAR HYPERPLASIA ( 1 FDA reports)
FOOD POISONING ( 1 FDA reports)
FORMICATION ( 1 FDA reports)
FRACTURE ( 1 FDA reports)
FUNGAL INFECTION ( 1 FDA reports)
FUNGAL OESOPHAGITIS ( 1 FDA reports)
FUNGAL SKIN INFECTION ( 1 FDA reports)
GAMMA-GLUTAMYLTRANSFERASE ABNORMAL ( 1 FDA reports)
GASTRIC CANCER ( 1 FDA reports)
GASTRIC DISORDER ( 1 FDA reports)
GASTRIC ULCER PERFORATION ( 1 FDA reports)
GASTROINTESTINAL ANGIODYSPLASIA ( 1 FDA reports)
GASTROOESOPHAGEAL REFLUX DISEASE ( 1 FDA reports)
GENERALISED OEDEMA ( 1 FDA reports)
GENITAL SWELLING ( 1 FDA reports)
GOUTY ARTHRITIS ( 1 FDA reports)
GRANULOCYTE COUNT DECREASED ( 1 FDA reports)
HAEMATOCRIT DECREASED ( 1 FDA reports)
HAEMATOTOXICITY ( 1 FDA reports)
HAEMORRHAGIC STROKE ( 1 FDA reports)
HALLUCINATION, VISUAL ( 1 FDA reports)
HEAD DISCOMFORT ( 1 FDA reports)
HEAD INJURY ( 1 FDA reports)
HEARING IMPAIRED ( 1 FDA reports)
HEART SOUNDS ABNORMAL ( 1 FDA reports)
HEPATIC ENZYME ABNORMAL ( 1 FDA reports)
HEPATIC FUNCTION ABNORMAL ( 1 FDA reports)
HEPATIC HAEMORRHAGE ( 1 FDA reports)
HEPATIC LESION ( 1 FDA reports)
HEPATOCELLULAR DAMAGE ( 1 FDA reports)
HERNIA OBSTRUCTIVE ( 1 FDA reports)
HIATUS HERNIA ( 1 FDA reports)
HICCUPS ( 1 FDA reports)
HIGH DENSITY LIPOPROTEIN DECREASED ( 1 FDA reports)
HOT FLUSH ( 1 FDA reports)
HYPERAESTHESIA ( 1 FDA reports)
HYPERPHAGIA ( 1 FDA reports)
HYPERSPLENISM ( 1 FDA reports)
HYPERTHERMIA ( 1 FDA reports)
HYPERTHYROIDISM ( 1 FDA reports)
HYPERVENTILATION ( 1 FDA reports)
HYPERVOLAEMIA ( 1 FDA reports)
HYPOCHROMIC ANAEMIA ( 1 FDA reports)
HYPOPERFUSION ( 1 FDA reports)
HYPOPHOSPHATAEMIA ( 1 FDA reports)
HYPOTHYROIDISM ( 1 FDA reports)
HYPOTONIA ( 1 FDA reports)
HYSTERECTOMY ( 1 FDA reports)
IGA NEPHROPATHY ( 1 FDA reports)
ILEUS PARALYTIC ( 1 FDA reports)
IMMUNE SYSTEM DISORDER ( 1 FDA reports)
IMPAIRED WORK ABILITY ( 1 FDA reports)
IMPLANT SITE INFLAMMATION ( 1 FDA reports)
INADEQUATE ANALGESIA ( 1 FDA reports)
INAPPROPRIATE SCHEDULE OF DRUG ADMINISTRATION ( 1 FDA reports)
INCONTINENCE ( 1 FDA reports)
INCORRECT DOSE ADMINISTERED ( 1 FDA reports)
INCORRECT ROUTE OF DRUG ADMINISTRATION ( 1 FDA reports)
INFECTIOUS PERITONITIS ( 1 FDA reports)
INFERIOR VENA CAVA DILATATION ( 1 FDA reports)
INHIBITORY DRUG INTERACTION ( 1 FDA reports)
INJECTION SITE HAEMATOMA ( 1 FDA reports)
INJECTION SITE HAEMORRHAGE ( 1 FDA reports)
INJECTION SITE INDURATION ( 1 FDA reports)
INJECTION SITE OEDEMA ( 1 FDA reports)
INJECTION SITE PHLEBITIS ( 1 FDA reports)
INTENTIONAL MISUSE ( 1 FDA reports)
INTERCOSTAL NEURALGIA ( 1 FDA reports)
INTERVERTEBRAL DISC COMPRESSION ( 1 FDA reports)
INTERVERTEBRAL DISCITIS ( 1 FDA reports)
INTESTINAL FISTULA ( 1 FDA reports)
INTESTINAL ISCHAEMIA ( 1 FDA reports)
INTESTINAL RESECTION ( 1 FDA reports)
INTESTINAL STEATOSIS ( 1 FDA reports)
INTRAOCULAR PRESSURE INCREASED ( 1 FDA reports)
IRON DEFICIENCY ANAEMIA ( 1 FDA reports)
ISCHAEMIA ( 1 FDA reports)
JOINT RANGE OF MOTION DECREASED ( 1 FDA reports)
KYPHOSIS ( 1 FDA reports)
LARGE INTESTINAL HAEMORRHAGE ( 1 FDA reports)
LARGE INTESTINAL ULCER HAEMORRHAGE ( 1 FDA reports)
LEFT VENTRICULAR DYSFUNCTION ( 1 FDA reports)
LEFT VENTRICULAR END-DIASTOLIC PRESSURE INCREASED ( 1 FDA reports)
LEFT VENTRICULAR FAILURE ( 1 FDA reports)
LEUKAEMIA ( 1 FDA reports)
LEUKOCYTOCLASTIC VASCULITIS ( 1 FDA reports)
LIGAMENT RUPTURE ( 1 FDA reports)
LIPASE INCREASED ( 1 FDA reports)
LOCAL SWELLING ( 1 FDA reports)
LOW DENSITY LIPOPROTEIN INCREASED ( 1 FDA reports)
LUMBAR RADICULOPATHY ( 1 FDA reports)
LUNG ADENOCARCINOMA STAGE II ( 1 FDA reports)
LUNG SQUAMOUS CELL CARCINOMA STAGE UNSPECIFIED ( 1 FDA reports)
LUPUS NEPHRITIS ( 1 FDA reports)
LYMPHADENOPATHY MEDIASTINAL ( 1 FDA reports)
LYMPHANGITIS ( 1 FDA reports)
LYMPHOCYTE COUNT DECREASED ( 1 FDA reports)
LYMPHOMA ( 1 FDA reports)
MACULAR OEDEMA ( 1 FDA reports)
MACULE ( 1 FDA reports)
MAJOR DEPRESSION ( 1 FDA reports)
MALIGNANT HYPERTENSION ( 1 FDA reports)
MALIGNANT MELANOMA IN SITU ( 1 FDA reports)
MATERNAL EXPOSURE TIMING UNSPECIFIED ( 1 FDA reports)
MECHANICAL ILEUS ( 1 FDA reports)
MEDIASTINOSCOPY ( 1 FDA reports)
MELANOCYTIC NAEVUS ( 1 FDA reports)
MENINGISM ( 1 FDA reports)
MENINGITIS BACTERIAL ( 1 FDA reports)
MENORRHAGIA ( 1 FDA reports)
MENSTRUATION IRREGULAR ( 1 FDA reports)
MENTAL IMPAIRMENT ( 1 FDA reports)
METASTASES TO BONE ( 1 FDA reports)
METASTASES TO LUNG ( 1 FDA reports)
METRORRHAGIA ( 1 FDA reports)
MICTURITION DISORDER ( 1 FDA reports)
MITRAL VALVE CALCIFICATION ( 1 FDA reports)
MOOD SWINGS ( 1 FDA reports)
MULTIPLE ENDOCRINE ADENOMATOSIS TYPE II ( 1 FDA reports)
MUSCLE ATROPHY ( 1 FDA reports)
MUSCLE SPASTICITY ( 1 FDA reports)
MUSCLE TWITCHING ( 1 FDA reports)
MUSCULOSKELETAL DISCOMFORT ( 1 FDA reports)
MYCOSIS FUNGOIDES STAGE I ( 1 FDA reports)
MYOGLOBIN URINE PRESENT ( 1 FDA reports)
MYOSCLEROSIS ( 1 FDA reports)
NASAL DRYNESS ( 1 FDA reports)
NASAL MUCOSAL DISORDER ( 1 FDA reports)
NECK INJURY ( 1 FDA reports)
NECK PAIN ( 1 FDA reports)
NECROTISING FASCIITIS ( 1 FDA reports)
NEOPLASM ( 1 FDA reports)
NEOPLASM PROGRESSION ( 1 FDA reports)
NEOPLASM RECURRENCE ( 1 FDA reports)
NEPHRITIC SYNDROME ( 1 FDA reports)
NEPHRITIS INTERSTITIAL ( 1 FDA reports)
NERVE INJURY ( 1 FDA reports)
NERVE ROOT COMPRESSION ( 1 FDA reports)
NEUTROPENIC SEPSIS ( 1 FDA reports)
NO ADVERSE EVENT ( 1 FDA reports)
NON-SMALL CELL LUNG CANCER ( 1 FDA reports)
OCCULT BLOOD POSITIVE ( 1 FDA reports)
OCULAR HYPERAEMIA ( 1 FDA reports)
OESOPHAGEAL ATRESIA ( 1 FDA reports)
OESOPHAGEAL CANDIDIASIS ( 1 FDA reports)
OESOPHAGEAL DISORDER ( 1 FDA reports)
ONYCHOCLASIS ( 1 FDA reports)
ONYCHOMYCOSIS ( 1 FDA reports)
OOPHORECTOMY ( 1 FDA reports)
OPEN WOUND ( 1 FDA reports)
OPTIC ATROPHY ( 1 FDA reports)
ORAL HERPES ( 1 FDA reports)
ORAL INTAKE REDUCED ( 1 FDA reports)
ORAL MUCOSAL BLISTERING ( 1 FDA reports)
ORGAN FAILURE ( 1 FDA reports)
ORGANISING PNEUMONIA ( 1 FDA reports)
ORTHOSTATIC HYPOTENSION ( 1 FDA reports)
OSTEOPOROTIC FRACTURE ( 1 FDA reports)
OVARIAN CYST ( 1 FDA reports)
PAIN MANAGEMENT ( 1 FDA reports)
PANCREATIC DISORDER ( 1 FDA reports)
PANOPHTHALMITIS ( 1 FDA reports)
PARAESTHESIA ORAL ( 1 FDA reports)
PARANOIA ( 1 FDA reports)
PARATHYROIDECTOMY ( 1 FDA reports)
PARESIS ( 1 FDA reports)
PARKINSONIAN GAIT ( 1 FDA reports)
PATENT DUCTUS ARTERIOSUS ( 1 FDA reports)
PELVIC MASS ( 1 FDA reports)
PERIODONTITIS ( 1 FDA reports)
PERIOSTITIS ( 1 FDA reports)
PERIPHERAL NERVE DECOMPRESSION ( 1 FDA reports)
PNEUMONIA LEGIONELLA ( 1 FDA reports)
PNEUMONIA PRIMARY ATYPICAL ( 1 FDA reports)
POLLAKIURIA ( 1 FDA reports)
POLYARTHRITIS ( 1 FDA reports)
POLYURIA ( 1 FDA reports)
PORTAL HYPERTENSION ( 1 FDA reports)
POST PROCEDURAL COMPLICATION ( 1 FDA reports)
POST PROCEDURAL DISCHARGE ( 1 FDA reports)
POST PROCEDURAL HAEMORRHAGE ( 1 FDA reports)
POST PROCEDURAL PULMONARY EMBOLISM ( 1 FDA reports)
POSTOPERATIVE INFECTION ( 1 FDA reports)
PRE-EXISTING CONDITION IMPROVED ( 1 FDA reports)
PREGNANCY OF PARTNER ( 1 FDA reports)
PRESBYOPIA ( 1 FDA reports)
PRODUCT QUALITY ISSUE ( 1 FDA reports)
PROSTATOMEGALY ( 1 FDA reports)
PSYCHOMOTOR SKILLS IMPAIRED ( 1 FDA reports)
PUBIS FRACTURE ( 1 FDA reports)
PULMONARY ALVEOLAR HAEMORRHAGE ( 1 FDA reports)
PULMONARY HAEMORRHAGE ( 1 FDA reports)
PULMONARY HILAR ENLARGEMENT ( 1 FDA reports)
PULPITIS DENTAL ( 1 FDA reports)
PUPILLARY LIGHT REFLEX TESTS ABNORMAL ( 1 FDA reports)
PURULENCE ( 1 FDA reports)
PYURIA ( 1 FDA reports)
RASH MORBILLIFORM ( 1 FDA reports)
RED BLOOD CELL AGGLUTINATION ( 1 FDA reports)
REFLUX OESOPHAGITIS ( 1 FDA reports)
RENAL HAEMORRHAGE ( 1 FDA reports)
RENAL VASCULITIS ( 1 FDA reports)
RENAL VENOUS CONGESTION ( 1 FDA reports)
RESPIRATION ABNORMAL ( 1 FDA reports)
RESPIRATORY DEPRESSION ( 1 FDA reports)
RETINAL DETACHMENT ( 1 FDA reports)
RETINAL VASCULAR THROMBOSIS ( 1 FDA reports)
RETINAL VEIN OCCLUSION ( 1 FDA reports)
RETROPERITONEAL LYMPHADENOPATHY ( 1 FDA reports)
RHINITIS ALLERGIC ( 1 FDA reports)
RIGHT VENTRICULAR FAILURE ( 1 FDA reports)
ROTAVIRUS INFECTION ( 1 FDA reports)
RUBELLA ANTIBODY POSITIVE ( 1 FDA reports)
SEBORRHOEIC KERATOSIS ( 1 FDA reports)
SENSE OF OPPRESSION ( 1 FDA reports)
SEROTONIN SYNDROME ( 1 FDA reports)
SERUM FERRITIN DECREASED ( 1 FDA reports)
SINUS RHYTHM ( 1 FDA reports)
SKIN BURNING SENSATION ( 1 FDA reports)
SKIN CANCER ( 1 FDA reports)
SKIN DISORDER ( 1 FDA reports)
SKIN HYPERTROPHY ( 1 FDA reports)
SKIN LESION ( 1 FDA reports)
SKIN REACTION ( 1 FDA reports)
SLEEP APNOEA SYNDROME ( 1 FDA reports)
SMALL CELL LUNG CANCER STAGE UNSPECIFIED ( 1 FDA reports)
SOFT TISSUE DISORDER ( 1 FDA reports)
SPINAL DEFORMITY ( 1 FDA reports)
SPINAL FUSION SURGERY ( 1 FDA reports)
SPONDYLOLISTHESIS ( 1 FDA reports)
STENOTROPHOMONAS TEST POSITIVE ( 1 FDA reports)
STREPTOCOCCAL SEPSIS ( 1 FDA reports)
SUDDEN DEATH ( 1 FDA reports)
SUDDEN HEARING LOSS ( 1 FDA reports)
SUPRAVENTRICULAR TACHYCARDIA ( 1 FDA reports)
SYSTEMIC LUPUS ERYTHEMATOSUS RASH ( 1 FDA reports)
SYSTOLIC HYPERTENSION ( 1 FDA reports)
TACHYCARDIA PAROXYSMAL ( 1 FDA reports)
TARDIVE DYSKINESIA ( 1 FDA reports)
TELANGIECTASIA ( 1 FDA reports)
TENDON DISORDER ( 1 FDA reports)
TENOSYNOVITIS ( 1 FDA reports)
THYROID NEOPLASM ( 1 FDA reports)
TONSILLAR DISORDER ( 1 FDA reports)
TOOTH INJURY ( 1 FDA reports)
TOOTHACHE ( 1 FDA reports)
TOXIC SKIN ERUPTION ( 1 FDA reports)
TRACHEO-OESOPHAGEAL FISTULA ( 1 FDA reports)
TRANSITIONAL CELL CARCINOMA ( 1 FDA reports)
TREATMENT NONCOMPLIANCE ( 1 FDA reports)
TRIGGER FINGER ( 1 FDA reports)
TROPONIN T INCREASED ( 1 FDA reports)
TUNNEL VISION ( 1 FDA reports)
UNEVALUABLE EVENT ( 1 FDA reports)
UNRESPONSIVE TO VERBAL STIMULI ( 1 FDA reports)
UPPER GASTROINTESTINAL HAEMORRHAGE ( 1 FDA reports)
URETERIC OBSTRUCTION ( 1 FDA reports)
URINE OUTPUT DECREASED ( 1 FDA reports)
UTERINE LEIOMYOMA ( 1 FDA reports)
UTERINE OPERATION ( 1 FDA reports)
UVEITIS ( 1 FDA reports)
VASCULAR OCCLUSION ( 1 FDA reports)
VASOCONSTRICTION ( 1 FDA reports)
VASODILATATION ( 1 FDA reports)
VERY LOW DENSITY LIPOPROTEIN INCREASED ( 1 FDA reports)
VIRAL PERICARDITIS ( 1 FDA reports)
VITAMIN B12 DEFICIENCY ( 1 FDA reports)
VITAMIN D INCREASED ( 1 FDA reports)
WALDENSTROM'S MACROGLOBULINAEMIA ( 1 FDA reports)
WOUND DEHISCENCE ( 1 FDA reports)
WOUND INFECTION ( 1 FDA reports)
WRONG TECHNIQUE IN DRUG USAGE PROCESS ( 1 FDA reports)

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