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

DRUG INTERACTION ( 40 FDA reports)
THROMBOCYTOPENIA ( 37 FDA reports)
ASTHENIA ( 35 FDA reports)
RENAL FAILURE ACUTE ( 35 FDA reports)
HYPOTENSION ( 32 FDA reports)
RENAL FAILURE ( 31 FDA reports)
CONFUSIONAL STATE ( 30 FDA reports)
VOMITING ( 30 FDA reports)
FALL ( 29 FDA reports)
PNEUMONIA ( 28 FDA reports)
MYALGIA ( 27 FDA reports)
DEHYDRATION ( 25 FDA reports)
ANAEMIA ( 24 FDA reports)
DYSPNOEA ( 24 FDA reports)
OVERDOSE ( 24 FDA reports)
DIARRHOEA ( 23 FDA reports)
DIZZINESS ( 23 FDA reports)
TREMOR ( 23 FDA reports)
URINARY RETENTION ( 23 FDA reports)
PYREXIA ( 22 FDA reports)
HYPERKALAEMIA ( 21 FDA reports)
NAUSEA ( 21 FDA reports)
OEDEMA PERIPHERAL ( 21 FDA reports)
GENERAL PHYSICAL HEALTH DETERIORATION ( 19 FDA reports)
MALAISE ( 19 FDA reports)
AGRANULOCYTOSIS ( 17 FDA reports)
NEUTROPENIA ( 17 FDA reports)
SEPTIC SHOCK ( 17 FDA reports)
DEATH ( 16 FDA reports)
DEPRESSION ( 16 FDA reports)
HAEMOGLOBIN DECREASED ( 16 FDA reports)
FATIGUE ( 15 FDA reports)
HALLUCINATION ( 15 FDA reports)
BENIGN PROSTATIC HYPERPLASIA ( 14 FDA reports)
CHOLESTASIS ( 14 FDA reports)
ATRIAL FIBRILLATION ( 13 FDA reports)
CARDIAC FAILURE ( 13 FDA reports)
CONDITION AGGRAVATED ( 13 FDA reports)
CYTOLYTIC HEPATITIS ( 13 FDA reports)
DRUG INEFFECTIVE ( 13 FDA reports)
PANCYTOPENIA ( 13 FDA reports)
RHABDOMYOLYSIS ( 13 FDA reports)
WEIGHT DECREASED ( 13 FDA reports)
AGITATION ( 12 FDA reports)
COMA ( 12 FDA reports)
DECREASED APPETITE ( 12 FDA reports)
DYSURIA ( 12 FDA reports)
HYPOKALAEMIA ( 12 FDA reports)
PULMONARY EMBOLISM ( 12 FDA reports)
RESPIRATORY FAILURE ( 12 FDA reports)
SOMNOLENCE ( 12 FDA reports)
ANXIETY ( 11 FDA reports)
BLOOD CREATININE INCREASED ( 11 FDA reports)
BLOOD PRESSURE DECREASED ( 11 FDA reports)
EOSINOPHILIA ( 11 FDA reports)
GAIT DISTURBANCE ( 11 FDA reports)
LUNG DISORDER ( 11 FDA reports)
MUSCULAR WEAKNESS ( 11 FDA reports)
PAIN ( 11 FDA reports)
SYNCOPE ( 11 FDA reports)
ARTHRALGIA ( 10 FDA reports)
BLOOD CREATINE PHOSPHOKINASE INCREASED ( 10 FDA reports)
CEREBROVASCULAR ACCIDENT ( 10 FDA reports)
COUGH ( 10 FDA reports)
HEPATITIS ( 10 FDA reports)
INTERNATIONAL NORMALISED RATIO INCREASED ( 10 FDA reports)
MELAENA ( 10 FDA reports)
NEOPLASM MALIGNANT ( 10 FDA reports)
PROSTATE CANCER ( 10 FDA reports)
SHOCK ( 10 FDA reports)
WITHDRAWAL SYNDROME ( 10 FDA reports)
CARDIAC ARREST ( 9 FDA reports)
CHEST PAIN ( 9 FDA reports)
DISEASE PROGRESSION ( 9 FDA reports)
DISORIENTATION ( 9 FDA reports)
GASTROINTESTINAL HAEMORRHAGE ( 9 FDA reports)
HYPERTENSION ( 9 FDA reports)
HYPOVOLAEMIC SHOCK ( 9 FDA reports)
IMMUNOSUPPRESSANT DRUG LEVEL INCREASED ( 9 FDA reports)
INSOMNIA ( 9 FDA reports)
LEUKOPENIA ( 9 FDA reports)
PURPURA ( 9 FDA reports)
SEPSIS ( 9 FDA reports)
TOXIC EPIDERMAL NECROLYSIS ( 9 FDA reports)
URINARY TRACT INFECTION ( 9 FDA reports)
AGGRESSION ( 8 FDA reports)
CARDIO-RESPIRATORY ARREST ( 8 FDA reports)
EPISTAXIS ( 8 FDA reports)
HEPATIC ENZYME INCREASED ( 8 FDA reports)
HEPATIC FAILURE ( 8 FDA reports)
LACTIC ACIDOSIS ( 8 FDA reports)
MUSCLE SPASMS ( 8 FDA reports)
NERVOUS SYSTEM DISORDER ( 8 FDA reports)
PROGRESSIVE MULTIFOCAL LEUKOENCEPHALOPATHY ( 8 FDA reports)
PRURITUS ( 8 FDA reports)
STEVENS-JOHNSON SYNDROME ( 8 FDA reports)
SUDDEN DEATH ( 8 FDA reports)
TOXIC SKIN ERUPTION ( 8 FDA reports)
TOXICITY TO VARIOUS AGENTS ( 8 FDA reports)
BLOOD BILIRUBIN INCREASED ( 7 FDA reports)
CIRCULATORY COLLAPSE ( 7 FDA reports)
DERMATITIS BULLOUS ( 7 FDA reports)
DRUG DISPENSING ERROR ( 7 FDA reports)
DRUG PRESCRIBING ERROR ( 7 FDA reports)
ENCEPHALOPATHY ( 7 FDA reports)
ERYTHEMA ( 7 FDA reports)
HYPONATRAEMIA ( 7 FDA reports)
HYPOPHAGIA ( 7 FDA reports)
MALNUTRITION ( 7 FDA reports)
MUCOSAL INFLAMMATION ( 7 FDA reports)
MULTIPLE SCLEROSIS RELAPSE ( 7 FDA reports)
NERVOUSNESS ( 7 FDA reports)
ORTHOSTATIC HYPOTENSION ( 7 FDA reports)
PETECHIAE ( 7 FDA reports)
PRODUCT SUBSTITUTION ISSUE ( 7 FDA reports)
RASH ( 7 FDA reports)
RASH ERYTHEMATOUS ( 7 FDA reports)
SUBDURAL HAEMATOMA ( 7 FDA reports)
SUICIDAL IDEATION ( 7 FDA reports)
TENDON RUPTURE ( 7 FDA reports)
ACUTE GENERALISED EXANTHEMATOUS PUSTULOSIS ( 6 FDA reports)
ALOPECIA ( 6 FDA reports)
ANGIOEDEMA ( 6 FDA reports)
ANURIA ( 6 FDA reports)
APLASIA PURE RED CELL ( 6 FDA reports)
ARRHYTHMIA ( 6 FDA reports)
ASCITES ( 6 FDA reports)
BLINDNESS ( 6 FDA reports)
BLOOD PRESSURE FLUCTUATION ( 6 FDA reports)
BONE MARROW FAILURE ( 6 FDA reports)
BRADYCARDIA ( 6 FDA reports)
CONVULSION ( 6 FDA reports)
CYSTIC LYMPHANGIOMA ( 6 FDA reports)
DIABETIC NEUROPATHY ( 6 FDA reports)
DRUG RASH WITH EOSINOPHILIA AND SYSTEMIC SYMPTOMS ( 6 FDA reports)
DYSPHAGIA ( 6 FDA reports)
EATING DISORDER ( 6 FDA reports)
FAECALOMA ( 6 FDA reports)
FEAR ( 6 FDA reports)
FINGER DEFORMITY ( 6 FDA reports)
FLUID INTAKE REDUCED ( 6 FDA reports)
HEADACHE ( 6 FDA reports)
HYDRONEPHROSIS ( 6 FDA reports)
HYPERPYREXIA ( 6 FDA reports)
HYPERTONIA ( 6 FDA reports)
HYPOALBUMINAEMIA ( 6 FDA reports)
INFLUENZA LIKE ILLNESS ( 6 FDA reports)
LEUKOCYTOSIS ( 6 FDA reports)
LOSS OF CONSCIOUSNESS ( 6 FDA reports)
LUNG INFECTION ( 6 FDA reports)
MEMORY IMPAIRMENT ( 6 FDA reports)
MYOCARDIAL INFARCTION ( 6 FDA reports)
MYOSITIS ( 6 FDA reports)
NEUROMYOPATHY ( 6 FDA reports)
PAIN IN EXTREMITY ( 6 FDA reports)
PARALYSIS ( 6 FDA reports)
POLLAKIURIA ( 6 FDA reports)
PROSTATOMEGALY ( 6 FDA reports)
RECTAL HAEMORRHAGE ( 6 FDA reports)
ACUTE PRERENAL FAILURE ( 5 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 5 FDA reports)
ARTHRITIS BACTERIAL ( 5 FDA reports)
CACHEXIA ( 5 FDA reports)
COLITIS ISCHAEMIC ( 5 FDA reports)
CRANIOCEREBRAL INJURY ( 5 FDA reports)
CYANOSIS ( 5 FDA reports)
DEEP VEIN THROMBOSIS ( 5 FDA reports)
DEMENTIA ALZHEIMER'S TYPE ( 5 FDA reports)
DEVICE RELATED SEPSIS ( 5 FDA reports)
ENTEROCOLITIS INFECTIOUS ( 5 FDA reports)
HAEMOPTYSIS ( 5 FDA reports)
HAEMORRHAGE INTRACRANIAL ( 5 FDA reports)
HEAD INJURY ( 5 FDA reports)
HEART RATE INCREASED ( 5 FDA reports)
HYPERHIDROSIS ( 5 FDA reports)
HYPERNATRAEMIA ( 5 FDA reports)
HYPERTHERMIA ( 5 FDA reports)
JAUNDICE ( 5 FDA reports)
LIBIDO DECREASED ( 5 FDA reports)
LYMPHADENOPATHY ( 5 FDA reports)
LYMPHOCELE ( 5 FDA reports)
MYELODYSPLASTIC SYNDROME ( 5 FDA reports)
NASOPHARYNGITIS ( 5 FDA reports)
NEOPLASM PROGRESSION ( 5 FDA reports)
OSTEONECROSIS ( 5 FDA reports)
PALLOR ( 5 FDA reports)
PANCREATITIS CHRONIC ( 5 FDA reports)
PEMPHIGOID ( 5 FDA reports)
PNEUMONITIS ( 5 FDA reports)
POST PROCEDURAL HAEMORRHAGE ( 5 FDA reports)
PROSTATITIS ( 5 FDA reports)
PSEUDOHYPERKALAEMIA ( 5 FDA reports)
RESPIRATORY ARREST ( 5 FDA reports)
SENSORY DISTURBANCE ( 5 FDA reports)
SUICIDE ATTEMPT ( 5 FDA reports)
TENDONITIS ( 5 FDA reports)
TRANSIENT ISCHAEMIC ATTACK ( 5 FDA reports)
URETERIC ANASTOMOSIS COMPLICATION ( 5 FDA reports)
URINARY HESITATION ( 5 FDA reports)
URINARY TRACT OBSTRUCTION ( 5 FDA reports)
URTICARIA ( 5 FDA reports)
VENTRICULAR FIBRILLATION ( 5 FDA reports)
VERTIGO ( 5 FDA reports)
VISUAL DISTURBANCE ( 5 FDA reports)
VOLVULUS ( 5 FDA reports)
ABDOMINAL PAIN ( 4 FDA reports)
ACUTE MYELOID LEUKAEMIA ( 4 FDA reports)
AGORAPHOBIA ( 4 FDA reports)
ANHEDONIA ( 4 FDA reports)
BACK PAIN ( 4 FDA reports)
BALANCE DISORDER ( 4 FDA reports)
BLADDER CATHETERISATION ( 4 FDA reports)
BLOOD UREA INCREASED ( 4 FDA reports)
CARDIAC DISORDER ( 4 FDA reports)
CEREBRAL HAEMORRHAGE ( 4 FDA reports)
CHILLS ( 4 FDA reports)
CLAUSTROPHOBIA ( 4 FDA reports)
COGNITIVE DISORDER ( 4 FDA reports)
CONSTIPATION ( 4 FDA reports)
CORONARY ARTERY DISEASE ( 4 FDA reports)
CYTOMEGALOVIRUS INFECTION ( 4 FDA reports)
DELIRIUM ( 4 FDA reports)
DELUSION ( 4 FDA reports)
DEMENTIA ( 4 FDA reports)
DRUG DEPENDENCE ( 4 FDA reports)
DYSPHONIA ( 4 FDA reports)
GASTRITIS ( 4 FDA reports)
HAEMATEMESIS ( 4 FDA reports)
HAEMATOMA ( 4 FDA reports)
HAEMODYNAMIC INSTABILITY ( 4 FDA reports)
HYPERCAPNIA ( 4 FDA reports)
HYPERSENSITIVITY ( 4 FDA reports)
HYPOPHARYNGEAL CANCER ( 4 FDA reports)
INTERSTITIAL LUNG DISEASE ( 4 FDA reports)
LOWER RESPIRATORY TRACT INFECTION ( 4 FDA reports)
LUNG NEOPLASM MALIGNANT ( 4 FDA reports)
LYMPHOMA ( 4 FDA reports)
MENTAL IMPAIRMENT ( 4 FDA reports)
METABOLIC ALKALOSIS ( 4 FDA reports)
METASTASES TO LUNG ( 4 FDA reports)
MUSCULOSKELETAL PAIN ( 4 FDA reports)
MUSCULOSKELETAL STIFFNESS ( 4 FDA reports)
NIGHT SWEATS ( 4 FDA reports)
OSTEONECROSIS OF JAW ( 4 FDA reports)
PAIN IN JAW ( 4 FDA reports)
PANCREATITIS ACUTE ( 4 FDA reports)
PARAESTHESIA ( 4 FDA reports)
PARANOIA ( 4 FDA reports)
PHOTOSENSITIVITY REACTION ( 4 FDA reports)
PLEURAL EFFUSION ( 4 FDA reports)
PNEUMONIA ASPIRATION ( 4 FDA reports)
RASH MACULO-PAPULAR ( 4 FDA reports)
SKIN LESION ( 4 FDA reports)
TOOTH EXTRACTION ( 4 FDA reports)
WEIGHT INCREASED ( 4 FDA reports)
WHITE BLOOD CELL COUNT DECREASED ( 4 FDA reports)
WHITE BLOOD CELL COUNT INCREASED ( 4 FDA reports)
WRONG DRUG ADMINISTERED ( 4 FDA reports)
ABDOMINAL PAIN UPPER ( 3 FDA reports)
ABDOMINAL WALL HAEMATOMA ( 3 FDA reports)
ABNORMAL BEHAVIOUR ( 3 FDA reports)
ACCIDENTAL OVERDOSE ( 3 FDA reports)
ACUTE CORONARY SYNDROME ( 3 FDA reports)
ACUTE RESPIRATORY DISTRESS SYNDROME ( 3 FDA reports)
AMNESIA ( 3 FDA reports)
ARRHYTHMIA SUPRAVENTRICULAR ( 3 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 3 FDA reports)
ATRIAL FLUTTER ( 3 FDA reports)
BACTERIAL TEST POSITIVE ( 3 FDA reports)
BLADDER CANCER RECURRENT ( 3 FDA reports)
BRONCHIAL OBSTRUCTION ( 3 FDA reports)
BRONCHITIS ( 3 FDA reports)
BRONCHOSPASM ( 3 FDA reports)
CHOLECYSTITIS ACUTE ( 3 FDA reports)
DEBRIDEMENT ( 3 FDA reports)
DEPRESSED LEVEL OF CONSCIOUSNESS ( 3 FDA reports)
DIABETES MELLITUS ( 3 FDA reports)
DRUG ADMINISTRATION ERROR ( 3 FDA reports)
DRUG WITHDRAWAL SYNDROME ( 3 FDA reports)
DYSGEUSIA ( 3 FDA reports)
DYSKINESIA ( 3 FDA reports)
DYSPNOEA EXERTIONAL ( 3 FDA reports)
ENDOMETRIAL CANCER ( 3 FDA reports)
EPILEPSY ( 3 FDA reports)
EYELID OEDEMA ( 3 FDA reports)
FAILURE TO THRIVE ( 3 FDA reports)
GASTRIC ULCER ( 3 FDA reports)
GASTROINTESTINAL INFECTION ( 3 FDA reports)
GASTROINTESTINAL ULCER ( 3 FDA reports)
GRAND MAL CONVULSION ( 3 FDA reports)
GYNAECOMASTIA ( 3 FDA reports)
HEPATITIS ACUTE ( 3 FDA reports)
HICCUPS ( 3 FDA reports)
HYPOAESTHESIA ( 3 FDA reports)
HYPOGLYCAEMIA ( 3 FDA reports)
IIIRD NERVE PARALYSIS ( 3 FDA reports)
INFARCTION ( 3 FDA reports)
JAUNDICE CHOLESTATIC ( 3 FDA reports)
METABOLIC ACIDOSIS ( 3 FDA reports)
MOVEMENT DISORDER ( 3 FDA reports)
MUSCLE ATROPHY ( 3 FDA reports)
NEPHROLITHIASIS ( 3 FDA reports)
NEPHROPATHY TOXIC ( 3 FDA reports)
NEUROMUSCULAR BLOCKADE ( 3 FDA reports)
OEDEMA ( 3 FDA reports)
OXYGEN SATURATION DECREASED ( 3 FDA reports)
PAROSMIA ( 3 FDA reports)
PLATELET COUNT DECREASED ( 3 FDA reports)
PROSTATIC SPECIFIC ANTIGEN INCREASED ( 3 FDA reports)
PROTEINURIA ( 3 FDA reports)
PSYCHOMOTOR HYPERACTIVITY ( 3 FDA reports)
PULMONARY FIBROSIS ( 3 FDA reports)
PULMONARY HYPERTENSION ( 3 FDA reports)
RASH PRURITIC ( 3 FDA reports)
RENAL DISORDER ( 3 FDA reports)
RESPIRATORY DISTRESS ( 3 FDA reports)
SEDATION ( 3 FDA reports)
SHOCK HAEMORRHAGIC ( 3 FDA reports)
SUPRAVENTRICULAR TACHYCARDIA ( 3 FDA reports)
THINKING ABNORMAL ( 3 FDA reports)
THYROID CANCER ( 3 FDA reports)
TRANSURETHRAL PROSTATECTOMY ( 3 FDA reports)
VASCULAR PURPURA ( 3 FDA reports)
VASCULITIS ( 3 FDA reports)
VENTRICULAR EXTRASYSTOLES ( 3 FDA reports)
VISION BLURRED ( 3 FDA reports)
WALKING DISABILITY ( 3 FDA reports)
AMYOTROPHIC LATERAL SCLEROSIS ( 2 FDA reports)
ANAL ABSCESS ( 2 FDA reports)
ANAPHYLACTIC REACTION ( 2 FDA reports)
ANAPHYLACTIC SHOCK ( 2 FDA reports)
ANASTOMOTIC HAEMORRHAGE ( 2 FDA reports)
ANGINA PECTORIS ( 2 FDA reports)
ANGIOGRAM ( 2 FDA reports)
ANOREXIA ( 2 FDA reports)
ANTI-ERYTHROPOIETIN ANTIBODY POSITIVE ( 2 FDA reports)
AORTIC DISSECTION ( 2 FDA reports)
APPETITE DISORDER ( 2 FDA reports)
ARTERIAL BRUIT ( 2 FDA reports)
ARTHRITIS ( 2 FDA reports)
ASPHYXIA ( 2 FDA reports)
ATRIOVENTRICULAR BLOCK ( 2 FDA reports)
ATTENTION DEFICIT/HYPERACTIVITY DISORDER ( 2 FDA reports)
B-CELL LYMPHOMA ( 2 FDA reports)
BLADDER NEOPLASM ( 2 FDA reports)
BLADDER OBSTRUCTION ( 2 FDA reports)
BLADDER PAIN ( 2 FDA reports)
BLINDNESS UNILATERAL ( 2 FDA reports)
BLOOD ALKALINE PHOSPHATASE INCREASED ( 2 FDA reports)
BREAST CYST ( 2 FDA reports)
BREATH SOUNDS ABNORMAL ( 2 FDA reports)
BRONCHOPNEUMONIA ( 2 FDA reports)
BUNDLE BRANCH BLOCK ( 2 FDA reports)
BUNDLE BRANCH BLOCK RIGHT ( 2 FDA reports)
C-REACTIVE PROTEIN INCREASED ( 2 FDA reports)
CATARACT ( 2 FDA reports)
CATHETER SITE HAEMORRHAGE ( 2 FDA reports)
CELLULITIS ( 2 FDA reports)
CEREBRAL TOXOPLASMOSIS ( 2 FDA reports)
CHOLECYSTITIS CHRONIC ( 2 FDA reports)
CHOLESTATIC LIVER INJURY ( 2 FDA reports)
COAGULOPATHY ( 2 FDA reports)
COLITIS ( 2 FDA reports)
COMPLETED SUICIDE ( 2 FDA reports)
COMPLICATIONS OF TRANSPLANTED KIDNEY ( 2 FDA reports)
CORONARY ANGIOPLASTY ( 2 FDA reports)
CRYING ( 2 FDA reports)
DERMATITIS ACNEIFORM ( 2 FDA reports)
DISTURBANCE IN ATTENTION ( 2 FDA reports)
DUODENITIS ( 2 FDA reports)
DYSPHORIA ( 2 FDA reports)
ECONOMIC PROBLEM ( 2 FDA reports)
EMBOLISM ( 2 FDA reports)
ENCEPHALITIS ( 2 FDA reports)
ENURESIS ( 2 FDA reports)
ESCHERICHIA SEPSIS ( 2 FDA reports)
FACE OEDEMA ( 2 FDA reports)
FLUID RETENTION ( 2 FDA reports)
GALLBLADDER OEDEMA ( 2 FDA reports)
GASTRITIS HAEMORRHAGIC ( 2 FDA reports)
GASTROINTESTINAL EROSION ( 2 FDA reports)
GENERAL PHYSICAL CONDITION ABNORMAL ( 2 FDA reports)
GENERALISED OEDEMA ( 2 FDA reports)
GINGIVAL BLEEDING ( 2 FDA reports)
GLOMERULAR FILTRATION RATE DECREASED ( 2 FDA reports)
HAEMATOCRIT DECREASED ( 2 FDA reports)
HAEMATOLOGICAL MALIGNANCY ( 2 FDA reports)
HAEMATURIA ( 2 FDA reports)
HAEMORRHOIDS ( 2 FDA reports)
HEART RATE DECREASED ( 2 FDA reports)
HEMIPLEGIA ( 2 FDA reports)
HEPATIC CIRRHOSIS ( 2 FDA reports)
HERPES VIRUS INFECTION ( 2 FDA reports)
HERPES ZOSTER ( 2 FDA reports)
HYPERAMMONAEMIA ( 2 FDA reports)
HYPERBILIRUBINAEMIA ( 2 FDA reports)
HYPERCALCAEMIA ( 2 FDA reports)
HYPERLACTACIDAEMIA ( 2 FDA reports)
HYPERTENSIVE CRISIS ( 2 FDA reports)
HYPOTHERMIA ( 2 FDA reports)
HYPOXIA ( 2 FDA reports)
HYPOXIC-ISCHAEMIC ENCEPHALOPATHY ( 2 FDA reports)
ILEITIS ( 2 FDA reports)
ILL-DEFINED DISORDER ( 2 FDA reports)
IMMUNE RECONSTITUTION SYNDROME ( 2 FDA reports)
IMPULSE-CONTROL DISORDER ( 2 FDA reports)
INCORRECT DOSE ADMINISTERED ( 2 FDA reports)
INFECTION ( 2 FDA reports)
INGUINAL HERNIA ( 2 FDA reports)
INGUINAL HERNIA REPAIR ( 2 FDA reports)
INITIAL INSOMNIA ( 2 FDA reports)
INTERVERTEBRAL DISC PROTRUSION ( 2 FDA reports)
INTRAOCULAR PRESSURE INCREASED ( 2 FDA reports)
IRIDOCYCLITIS ( 2 FDA reports)
ISCHAEMIC STROKE ( 2 FDA reports)
JOINT INJURY ( 2 FDA reports)
JOINT SWELLING ( 2 FDA reports)
KIDNEY TRANSPLANT REJECTION ( 2 FDA reports)
LARGE INTESTINAL ULCER HAEMORRHAGE ( 2 FDA reports)
LARYNGOSPASM ( 2 FDA reports)
LEUKAEMIA ( 2 FDA reports)
LIPOSARCOMA ( 2 FDA reports)
LIVER ABSCESS ( 2 FDA reports)
LIVER DISORDER ( 2 FDA reports)
LIVER INJURY ( 2 FDA reports)
LUNG CONSOLIDATION ( 2 FDA reports)
LYMPH NODE PAIN ( 2 FDA reports)
LYMPHOCYTE COUNT DECREASED ( 2 FDA reports)
MALIGNANT NEOPLASM PROGRESSION ( 2 FDA reports)
MEDICATION ERROR ( 2 FDA reports)
MENINGISM ( 2 FDA reports)
MENINGITIS ( 2 FDA reports)
MENTAL DISORDER ( 2 FDA reports)
MICTURITION URGENCY ( 2 FDA reports)
MIOSIS ( 2 FDA reports)
MITRAL VALVE INCOMPETENCE ( 2 FDA reports)
MULTIPLE MYELOMA ( 2 FDA reports)
MUSCLE HAEMORRHAGE ( 2 FDA reports)
MYOPATHY ( 2 FDA reports)
NEUTROPHIL COUNT INCREASED ( 2 FDA reports)
NIKOLSKY'S SIGN ( 2 FDA reports)
NOCTURIA ( 2 FDA reports)
NON-SMALL CELL LUNG CANCER ( 2 FDA reports)
NORMOCHROMIC NORMOCYTIC ANAEMIA ( 2 FDA reports)
OBESITY ( 2 FDA reports)
OESOPHAGEAL DISORDER ( 2 FDA reports)
OFF LABEL USE ( 2 FDA reports)
ORAL DISORDER ( 2 FDA reports)
OROPHARYNGEAL DISCOMFORT ( 2 FDA reports)
OSTEOARTHRITIS ( 2 FDA reports)
OSTEOMYELITIS ( 2 FDA reports)
PALPITATIONS ( 2 FDA reports)
PANCREATIC CARCINOMA ( 2 FDA reports)
PANCREATITIS ( 2 FDA reports)
PEMPHIGUS ( 2 FDA reports)
PHOTOPHOBIA ( 2 FDA reports)
PLATELET COUNT INCREASED ( 2 FDA reports)
PLATELET DISORDER ( 2 FDA reports)
PNEUMONIA PRIMARY ATYPICAL ( 2 FDA reports)
PNEUMOTHORAX ( 2 FDA reports)
POLYURIA ( 2 FDA reports)
POOR QUALITY SLEEP ( 2 FDA reports)
PROSTATE CANCER METASTATIC ( 2 FDA reports)
PROSTATISM ( 2 FDA reports)
PROTHROMBIN TIME PROLONGED ( 2 FDA reports)
PRURITUS GENERALISED ( 2 FDA reports)
PULMONARY ALVEOLAR HAEMORRHAGE ( 2 FDA reports)
PUNCTURE SITE HAEMORRHAGE ( 2 FDA reports)
QUALITY OF LIFE DECREASED ( 2 FDA reports)
RENAL IMPAIRMENT ( 2 FDA reports)
RESTLESSNESS ( 2 FDA reports)
RETINAL ARTERY OCCLUSION ( 2 FDA reports)
RETINAL ISCHAEMIA ( 2 FDA reports)
RETINAL PIGMENT EPITHELIAL TEAR ( 2 FDA reports)
RETROPERITONEAL HAEMATOMA ( 2 FDA reports)
RIB FRACTURE ( 2 FDA reports)
SLEEP DISORDER ( 2 FDA reports)
SMALL CELL LUNG CANCER STAGE UNSPECIFIED ( 2 FDA reports)
SPLENOMEGALY ( 2 FDA reports)
STAPHYLOCOCCAL INFECTION ( 2 FDA reports)
STENT PLACEMENT ( 2 FDA reports)
STOOL ANALYSIS ABNORMAL ( 2 FDA reports)
STRESS ( 2 FDA reports)
STRIDOR ( 2 FDA reports)
SUICIDAL BEHAVIOUR ( 2 FDA reports)
SWELLING ( 2 FDA reports)
SWOLLEN TONGUE ( 2 FDA reports)
TONSILLITIS ( 2 FDA reports)
TOOTH DISORDER ( 2 FDA reports)
TOOTH LOSS ( 2 FDA reports)
TREATMENT NONCOMPLIANCE ( 2 FDA reports)
TROPONIN INCREASED ( 2 FDA reports)
UNEVALUABLE EVENT ( 2 FDA reports)
UNRESPONSIVE TO STIMULI ( 2 FDA reports)
URETHRAL INJURY ( 2 FDA reports)
URETHRAL STENOSIS ( 2 FDA reports)
URINARY BLADDER POLYP ( 2 FDA reports)
URINE FLOW DECREASED ( 2 FDA reports)
URINE OUTPUT INCREASED ( 2 FDA reports)
UROGENITAL HAEMORRHAGE ( 2 FDA reports)
UROSEPSIS ( 2 FDA reports)
VARICES OESOPHAGEAL ( 2 FDA reports)
VEIN DISORDER ( 2 FDA reports)
VENTRICULAR TACHYCARDIA ( 2 FDA reports)
WHEEZING ( 2 FDA reports)
WOUND DEHISCENCE ( 2 FDA reports)
WRONG TECHNIQUE IN DRUG USAGE PROCESS ( 2 FDA reports)
ABDOMINAL DISTENSION ( 1 FDA reports)
ABDOMINAL PAIN LOWER ( 1 FDA reports)
ACCIDENTAL EXPOSURE ( 1 FDA reports)
ACUTE MYOCARDIAL INFARCTION ( 1 FDA reports)
ACUTE PULMONARY OEDEMA ( 1 FDA reports)
ADRENAL INSUFFICIENCY ( 1 FDA reports)
ADRENAL NEOPLASM ( 1 FDA reports)
AGEUSIA ( 1 FDA reports)
AKATHISIA ( 1 FDA reports)
ANGER ( 1 FDA reports)
AORTIC VALVE INCOMPETENCE ( 1 FDA reports)
APATHY ( 1 FDA reports)
APHASIA ( 1 FDA reports)
APNOEA ( 1 FDA reports)
ARTERIAL HAEMORRHAGE ( 1 FDA reports)
ARTERIOVENOUS MALFORMATION ( 1 FDA reports)
ATELECTASIS ( 1 FDA reports)
ATRIOVENTRICULAR BLOCK COMPLETE ( 1 FDA reports)
ATRIOVENTRICULAR BLOCK FIRST DEGREE ( 1 FDA reports)
ATRIOVENTRICULAR BLOCK SECOND DEGREE ( 1 FDA reports)
ATYPICAL MYCOBACTERIAL INFECTION ( 1 FDA reports)
AZOTAEMIA ( 1 FDA reports)
BACTERAEMIA ( 1 FDA reports)
BICYTOPENIA ( 1 FDA reports)
BIOPSY PROSTATE ( 1 FDA reports)
BLADDER DISCOMFORT ( 1 FDA reports)
BLADDER DISORDER ( 1 FDA reports)
BLEPHARITIS ( 1 FDA reports)
BLINDNESS TRANSIENT ( 1 FDA reports)
BLISTER ( 1 FDA reports)
BLOOD AMYLASE INCREASED ( 1 FDA reports)
BLOOD CALCIUM DECREASED ( 1 FDA reports)
BLOOD CORTISOL DECREASED ( 1 FDA reports)
BLOOD CREATINE INCREASED ( 1 FDA reports)
BLOOD CREATINE PHOSPHOKINASE MB ( 1 FDA reports)
BLOOD GLUCOSE INCREASED ( 1 FDA reports)
BLOOD LACTATE DEHYDROGENASE INCREASED ( 1 FDA reports)
BLOOD POTASSIUM INCREASED ( 1 FDA reports)
BLOOD PRESSURE INCREASED ( 1 FDA reports)
BLOOD PRESSURE ORTHOSTATIC ABNORMAL ( 1 FDA reports)
BLOOD PRESSURE SYSTOLIC INCREASED ( 1 FDA reports)
BLOOD TEST ABNORMAL ( 1 FDA reports)
BLOOD UREA ABNORMAL ( 1 FDA reports)
BLOOD URINE PRESENT ( 1 FDA reports)
BODY TEMPERATURE INCREASED ( 1 FDA reports)
BONE LESION ( 1 FDA reports)
BONE MARROW TRANSPLANT ( 1 FDA reports)
BOTULISM ( 1 FDA reports)
BOVINE TUBERCULOSIS ( 1 FDA reports)
BRAIN OEDEMA ( 1 FDA reports)
BREAST CALCIFICATIONS ( 1 FDA reports)
BREAST NEOPLASM ( 1 FDA reports)
BREAST PAIN ( 1 FDA reports)
BRUXISM ( 1 FDA reports)
BURSITIS ( 1 FDA reports)
CALCINOSIS ( 1 FDA reports)
CARDIAC ENZYMES INCREASED ( 1 FDA reports)
CARDIAC FAILURE CONGESTIVE ( 1 FDA reports)
CAROTID ARTERY OCCLUSION ( 1 FDA reports)
CENTRAL NERVOUS SYSTEM LESION ( 1 FDA reports)
CENTRAL OBESITY ( 1 FDA reports)
CEREBRAL ISCHAEMIA ( 1 FDA reports)
CHEILITIS ( 1 FDA reports)
CHEST DISCOMFORT ( 1 FDA reports)
CHOKING ( 1 FDA reports)
CHONDROPATHY ( 1 FDA reports)
CHROMATURIA ( 1 FDA reports)
CHRONIC HEPATITIS ( 1 FDA reports)
CHRONIC LYMPHOCYTIC LEUKAEMIA ( 1 FDA reports)
CHRONIC MYELOID LEUKAEMIA ( 1 FDA reports)
COLON CANCER ( 1 FDA reports)
COLON CANCER METASTATIC ( 1 FDA reports)
COMMUNICATION DISORDER ( 1 FDA reports)
CONCOMITANT DISEASE AGGRAVATED ( 1 FDA reports)
CONCOMITANT DISEASE PROGRESSION ( 1 FDA reports)
CONCUSSION ( 1 FDA reports)
CONGESTIVE CARDIOMYOPATHY ( 1 FDA reports)
CONJUNCTIVAL OEDEMA ( 1 FDA reports)
CONJUNCTIVAL PALLOR ( 1 FDA reports)
CONTINUOUS HAEMODIAFILTRATION ( 1 FDA reports)
CONTRAINDICATION TO MEDICAL TREATMENT ( 1 FDA reports)
CREATININE RENAL CLEARANCE DECREASED ( 1 FDA reports)
CULTURE WOUND POSITIVE ( 1 FDA reports)
CUSHING'S SYNDROME ( 1 FDA reports)
CUSHINGOID ( 1 FDA reports)
CYSTOGRAM ABNORMAL ( 1 FDA reports)
DERMATITIS ( 1 FDA reports)
DERMATITIS ALLERGIC ( 1 FDA reports)
DERMATITIS EXFOLIATIVE ( 1 FDA reports)
DEVICE RELATED INFECTION ( 1 FDA reports)
DIPLOPIA ( 1 FDA reports)
DISCOMFORT ( 1 FDA reports)
DIVERTICULUM ( 1 FDA reports)
DIVERTICULUM INTESTINAL ( 1 FDA reports)
DRUG DOSE OMISSION ( 1 FDA reports)
DRUG EFFECT DECREASED ( 1 FDA reports)
DRUG HYPERSENSITIVITY ( 1 FDA reports)
DRUG LEVEL BELOW THERAPEUTIC ( 1 FDA reports)
DRUG LEVEL INCREASED ( 1 FDA reports)
DRY MOUTH ( 1 FDA reports)
DYSARTHRIA ( 1 FDA reports)
DYSPEPSIA ( 1 FDA reports)
DYSSTASIA ( 1 FDA reports)
EJECTION FRACTION DECREASED ( 1 FDA reports)
ELECTROCARDIOGRAM QT PROLONGED ( 1 FDA reports)
EMOTIONAL DISORDER ( 1 FDA reports)
EMOTIONAL DISTRESS ( 1 FDA reports)
ENDOCARDITIS ( 1 FDA reports)
ENDOSCOPY ( 1 FDA reports)
ENTEROCOCCUS TEST POSITIVE ( 1 FDA reports)
EPIDERMAL NECROSIS ( 1 FDA reports)
ERYTHROMELALGIA ( 1 FDA reports)
ERYTHROSIS ( 1 FDA reports)
ESCHAR ( 1 FDA reports)
EXOSTOSIS ( 1 FDA reports)
EXPOSED BONE IN JAW ( 1 FDA reports)
EXTERNAL EAR INFLAMMATION ( 1 FDA reports)
EXTRAPYRAMIDAL DISORDER ( 1 FDA reports)
EYE DISORDER ( 1 FDA reports)
EYELID PTOSIS ( 1 FDA reports)
FAMILY STRESS ( 1 FDA reports)
FANCONI SYNDROME ACQUIRED ( 1 FDA reports)
FEELING ABNORMAL ( 1 FDA reports)
FEMUR FRACTURE ( 1 FDA reports)
FIXED ERUPTION ( 1 FDA reports)
FLANK PAIN ( 1 FDA reports)
FLUSHING ( 1 FDA reports)
FOREIGN BODY ( 1 FDA reports)
FULL BLOOD COUNT ABNORMAL ( 1 FDA reports)
FUNGAL INFECTION ( 1 FDA reports)
GAMMA-GLUTAMYLTRANSFERASE INCREASED ( 1 FDA reports)
GAMMOPATHY ( 1 FDA reports)
GANGRENE ( 1 FDA reports)
GASTRIC PERFORATION ( 1 FDA reports)
GASTRIC POLYPS ( 1 FDA reports)
GASTRIC VARICES ( 1 FDA reports)
GASTRITIS EROSIVE ( 1 FDA reports)
GASTROINTESTINAL MUCOSAL DISORDER ( 1 FDA reports)
GASTROINTESTINAL TOXICITY ( 1 FDA reports)
GINGIVAL INFECTION ( 1 FDA reports)
GINGIVITIS ( 1 FDA reports)
GOUT ( 1 FDA reports)
GROIN PAIN ( 1 FDA reports)
HAEMOLYTIC ANAEMIA ( 1 FDA reports)
HAEMOPHILUS INFECTION ( 1 FDA reports)
HAEMORRHAGIC ANAEMIA ( 1 FDA reports)
HALLUCINATION, VISUAL ( 1 FDA reports)
HAPTOGLOBIN INCREASED ( 1 FDA reports)
HEAD DISCOMFORT ( 1 FDA reports)
HEART RATE IRREGULAR ( 1 FDA reports)
HEPATIC ENCEPHALOPATHY ( 1 FDA reports)
HEPATIC ENZYME ABNORMAL ( 1 FDA reports)
HEPATIC NEOPLASM ( 1 FDA reports)
HEPATIC NEOPLASM MALIGNANT ( 1 FDA reports)
HEPATIC STEATOSIS ( 1 FDA reports)
HEPATITIS B ( 1 FDA reports)
HEPATOCELLULAR INJURY ( 1 FDA reports)
HEPATOMEGALY ( 1 FDA reports)
HIP ARTHROPLASTY ( 1 FDA reports)
HOT FLUSH ( 1 FDA reports)
HYPERCHOLESTEROLAEMIA ( 1 FDA reports)
HYPERLIPIDAEMIA ( 1 FDA reports)
HYPERTENSIVE HEART DISEASE ( 1 FDA reports)
HYPERTONIC BLADDER ( 1 FDA reports)
HYPERTRANSAMINASAEMIA ( 1 FDA reports)
HYPERTROPHY ( 1 FDA reports)
HYPERVENTILATION ( 1 FDA reports)
HYPOCAPNIA ( 1 FDA reports)
HYPOSMIA ( 1 FDA reports)
HYPOTHROMBINAEMIA ( 1 FDA reports)
HYPOVOLAEMIA ( 1 FDA reports)
IMPETIGO ( 1 FDA reports)
INCONTINENCE ( 1 FDA reports)
INCREASED BRONCHIAL SECRETION ( 1 FDA reports)
INCREASED UPPER AIRWAY SECRETION ( 1 FDA reports)
INFECTION PARASITIC ( 1 FDA reports)
INFECTION SUSCEPTIBILITY INCREASED ( 1 FDA reports)
INFLAMMATION ( 1 FDA reports)
INFUSION RELATED REACTION ( 1 FDA reports)
INJECTION SITE ERYTHEMA ( 1 FDA reports)
INJECTION SITE INDURATION ( 1 FDA reports)
INJECTION SITE INFLAMMATION ( 1 FDA reports)
INJECTION SITE PAIN ( 1 FDA reports)
INJECTION SITE WARMTH ( 1 FDA reports)
INJURY ( 1 FDA reports)
INTENTIONAL OVERDOSE ( 1 FDA reports)
INTERNATIONAL NORMALISED RATIO DECREASED ( 1 FDA reports)
IRON DEFICIENCY ( 1 FDA reports)
IRRITABILITY ( 1 FDA reports)
JUGULAR VEIN THROMBOSIS ( 1 FDA reports)
KLEBSIELLA INFECTION ( 1 FDA reports)
LEFT VENTRICULAR FAILURE ( 1 FDA reports)
LEFT VENTRICULAR HYPERTROPHY ( 1 FDA reports)
LETHARGY ( 1 FDA reports)
LICHENOID KERATOSIS ( 1 FDA reports)
LIP OEDEMA ( 1 FDA reports)
LIPASE INCREASED ( 1 FDA reports)
LIVER FUNCTION TEST ABNORMAL ( 1 FDA reports)
LUNG CANCER METASTATIC ( 1 FDA reports)
LUNG INFILTRATION ( 1 FDA reports)
LUNG SQUAMOUS CELL CARCINOMA STAGE UNSPECIFIED ( 1 FDA reports)
LYMPHOPENIA ( 1 FDA reports)
MACULAR OEDEMA ( 1 FDA reports)
MALLORY-WEISS SYNDROME ( 1 FDA reports)
MASTICATION DISORDER ( 1 FDA reports)
MEDICAL OBSERVATION ABNORMAL ( 1 FDA reports)
MENINGITIS ASEPTIC ( 1 FDA reports)
METASTASES TO LIVER ( 1 FDA reports)
METASTASES TO LYMPH NODES ( 1 FDA reports)
METASTATIC NEOPLASM ( 1 FDA reports)
MIGRAINE ( 1 FDA reports)
MOOD ALTERED ( 1 FDA reports)
MULTI-ORGAN FAILURE ( 1 FDA reports)
MULTIPLE SCLEROSIS ( 1 FDA reports)
MUSCLE CONTRACTIONS INVOLUNTARY ( 1 FDA reports)
MUTISM ( 1 FDA reports)
MYOCARDIAL ISCHAEMIA ( 1 FDA reports)
MYOGLOBIN BLOOD INCREASED ( 1 FDA reports)
MYOPIA ( 1 FDA reports)
NASOPHARYNGEAL CANCER RECURRENT ( 1 FDA reports)
NECK DEFORMITY ( 1 FDA reports)
NECK PAIN ( 1 FDA reports)
NECROSIS ( 1 FDA reports)
NECROTISING RETINITIS ( 1 FDA reports)
NEPHRITIS INTERSTITIAL ( 1 FDA reports)
NEURALGIA ( 1 FDA reports)
NEURODEGENERATIVE DISORDER ( 1 FDA reports)
NEUROLOGICAL DECOMPENSATION ( 1 FDA reports)
NO ADVERSE EVENT ( 1 FDA reports)
NOCTURNAL DYSPNOEA ( 1 FDA reports)
NODULE ( 1 FDA reports)
NORMAL TENSION GLAUCOMA ( 1 FDA reports)
NUCLEAR MAGNETIC RESONANCE IMAGING ABNORMAL ( 1 FDA reports)
OCCULT BLOOD POSITIVE ( 1 FDA reports)
OESOPHAGEAL CANDIDIASIS ( 1 FDA reports)
OESOPHAGEAL ULCER ( 1 FDA reports)
OESOPHAGEAL VARICEAL LIGATION ( 1 FDA reports)
OESOPHAGITIS ( 1 FDA reports)
OESOPHAGITIS ULCERATIVE ( 1 FDA reports)
OLIGURIA ( 1 FDA reports)
OPTIC ATROPHY ( 1 FDA reports)
OPTIC DISC DISORDER ( 1 FDA reports)
OPTIC NEURITIS ( 1 FDA reports)
ORAL HERPES ( 1 FDA reports)
ORAL INTAKE REDUCED ( 1 FDA reports)
ORCHITIS ( 1 FDA reports)
OTITIS EXTERNA ( 1 FDA reports)
PALMAR ERYTHEMA ( 1 FDA reports)
PANCREATIC DISORDER ( 1 FDA reports)
PANCREATIC ENZYMES INCREASED ( 1 FDA reports)
PANCREATIC NECROSIS ( 1 FDA reports)
PANCREATOLITHIASIS ( 1 FDA reports)
PARACENTESIS ABDOMEN ( 1 FDA reports)
PARAPROTEINAEMIA ( 1 FDA reports)
PARKINSONISM ( 1 FDA reports)
PATHOGEN RESISTANCE ( 1 FDA reports)
PELVIC PAIN ( 1 FDA reports)
PEPTIC ULCER ( 1 FDA reports)
PERCUTANEOUS CORONARY INTERVENTION ( 1 FDA reports)
PERINEAL PAIN ( 1 FDA reports)
PERITONEAL EFFUSION ( 1 FDA reports)
PERONEAL NERVE PALSY ( 1 FDA reports)
PERSONALITY CHANGE ( 1 FDA reports)
PHARYNGEAL OEDEMA ( 1 FDA reports)
PLEURITIC PAIN ( 1 FDA reports)
PNEUMONIA BACTERIAL ( 1 FDA reports)
PNEUMONIA ESCHERICHIA ( 1 FDA reports)
POLYP ( 1 FDA reports)
POSTURE ABNORMAL ( 1 FDA reports)
POTENTIATING DRUG INTERACTION ( 1 FDA reports)
PREDISPOSITION TO DISEASE ( 1 FDA reports)
PRESYNCOPE ( 1 FDA reports)
PROCTOCOLITIS ( 1 FDA reports)
PRODUCT QUALITY ISSUE ( 1 FDA reports)
PRODUCTIVE COUGH ( 1 FDA reports)
PROSTATIC DISORDER ( 1 FDA reports)
PSYCHOTIC DISORDER ( 1 FDA reports)
PULMONARY INFARCTION ( 1 FDA reports)
PULMONARY OEDEMA ( 1 FDA reports)
PULMONARY TOXICITY ( 1 FDA reports)
PULMONARY TUBERCULOSIS ( 1 FDA reports)
RALES ( 1 FDA reports)
RASH PAPULAR ( 1 FDA reports)
RASH PUSTULAR ( 1 FDA reports)
RED BLOOD CELL COUNT DECREASED ( 1 FDA reports)
RED MAN SYNDROME ( 1 FDA reports)
RENAL CANCER ( 1 FDA reports)
RENAL FAILURE CHRONIC ( 1 FDA reports)
RENAL TUBULAR NECROSIS ( 1 FDA reports)
RENAL VESSEL DISORDER ( 1 FDA reports)
RESPIRATORY DISORDER ( 1 FDA reports)
RETINAL DEGENERATION ( 1 FDA reports)
RETINAL HAEMORRHAGE ( 1 FDA reports)
RHEUMATOID ARTHRITIS ( 1 FDA reports)
ROAD TRAFFIC ACCIDENT ( 1 FDA reports)
SCAR ( 1 FDA reports)
SCIATICA ( 1 FDA reports)
SERUM FERRITIN INCREASED ( 1 FDA reports)
SEXUAL DYSFUNCTION ( 1 FDA reports)
SINUS BRADYCARDIA ( 1 FDA reports)
SINUSITIS ( 1 FDA reports)
SKIN ATROPHY ( 1 FDA reports)
SKIN MACERATION ( 1 FDA reports)
SKIN NECROSIS ( 1 FDA reports)
SKIN PLAQUE ( 1 FDA reports)
SKIN REACTION ( 1 FDA reports)
SKIN STRIAE ( 1 FDA reports)
SKIN ULCER ( 1 FDA reports)
SPEECH DISORDER ( 1 FDA reports)
SPINAL OSTEOARTHRITIS ( 1 FDA reports)
SPLENIC INFARCTION ( 1 FDA reports)
SPUTUM PURULENT ( 1 FDA reports)
STOMATITIS ( 1 FDA reports)
SUBCORNEAL PUSTULAR DERMATOSIS ( 1 FDA reports)
SUBILEUS ( 1 FDA reports)
SUPERINFECTION ( 1 FDA reports)
SUPRAVENTRICULAR EXTRASYSTOLES ( 1 FDA reports)
SURGICAL FAILURE ( 1 FDA reports)
TABLET PHYSICAL ISSUE ( 1 FDA reports)
TACHYCARDIA ( 1 FDA reports)
TENDERNESS ( 1 FDA reports)
TENSION ( 1 FDA reports)
THERAPEUTIC AGENT TOXICITY ( 1 FDA reports)
THROMBOSIS ( 1 FDA reports)
THROMBOTIC THROMBOCYTOPENIC PURPURA ( 1 FDA reports)
TINNITUS ( 1 FDA reports)
TONGUE DRY ( 1 FDA reports)
TORSADE DE POINTES ( 1 FDA reports)
TRACHEAL DEVIATION ( 1 FDA reports)
TRACHEOBRONCHITIS ( 1 FDA reports)
TRANSAMINASES INCREASED ( 1 FDA reports)
TRANSPLANT REJECTION ( 1 FDA reports)
TRICUSPID VALVE INCOMPETENCE ( 1 FDA reports)
TROPONIN T INCREASED ( 1 FDA reports)
TUBERCULOSIS ( 1 FDA reports)
TUBULOINTERSTITIAL NEPHRITIS ( 1 FDA reports)
TYPE I HYPERSENSITIVITY ( 1 FDA reports)
ULCER HAEMORRHAGE ( 1 FDA reports)
UNDERDOSE ( 1 FDA reports)
UPPER RESPIRATORY TRACT INFECTION ( 1 FDA reports)
URINE ANALYSIS ABNORMAL ( 1 FDA reports)
VASCULAR GRAFT ( 1 FDA reports)
VASCULAR INJURY ( 1 FDA reports)
VENOUS HAEMORRHAGE ( 1 FDA reports)
VENOUS INJURY ( 1 FDA reports)
VISUAL IMPAIRMENT ( 1 FDA reports)
WOUND ( 1 FDA reports)
WOUND COMPLICATION ( 1 FDA reports)
WOUND DEBRIDEMENT ( 1 FDA reports)

© 2014 MedsFacts, Inc
Privacy Policy
Terms of Use