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

DYSPNOEA ( 44 FDA reports)
RENAL FAILURE ( 37 FDA reports)
PYREXIA ( 35 FDA reports)
PNEUMONIA ( 31 FDA reports)
COUGH ( 30 FDA reports)
PAIN ( 28 FDA reports)
GASTROINTESTINAL HAEMORRHAGE ( 27 FDA reports)
PAIN IN EXTREMITY ( 27 FDA reports)
MUSCULAR WEAKNESS ( 26 FDA reports)
SEPSIS ( 26 FDA reports)
ACUTE RESPIRATORY FAILURE ( 25 FDA reports)
ANAEMIA ( 24 FDA reports)
BLOOD UREA INCREASED ( 24 FDA reports)
CARDIAC FAILURE CONGESTIVE ( 24 FDA reports)
HAEMOGLOBIN DECREASED ( 22 FDA reports)
HAEMOPTYSIS ( 22 FDA reports)
MELAENA ( 21 FDA reports)
MYALGIA ( 18 FDA reports)
NAUSEA ( 18 FDA reports)
PULMONARY EMBOLISM ( 18 FDA reports)
RENAL FAILURE ACUTE ( 18 FDA reports)
WEGENER'S GRANULOMATOSIS ( 18 FDA reports)
GENERAL PHYSICAL HEALTH DETERIORATION ( 17 FDA reports)
MOBILITY DECREASED ( 17 FDA reports)
NEPHROGENIC SYSTEMIC FIBROSIS ( 17 FDA reports)
OEDEMA PERIPHERAL ( 17 FDA reports)
DIZZINESS ( 16 FDA reports)
SKIN INDURATION ( 15 FDA reports)
ANXIETY ( 14 FDA reports)
CHEST PAIN ( 14 FDA reports)
DEATH ( 14 FDA reports)
EMOTIONAL DISTRESS ( 14 FDA reports)
FATIGUE ( 13 FDA reports)
HEADACHE ( 13 FDA reports)
HYPOTENSION ( 13 FDA reports)
VOMITING ( 13 FDA reports)
SKIN HYPERTROPHY ( 12 FDA reports)
ATRIAL FIBRILLATION ( 11 FDA reports)
CARDIAC FAILURE ( 11 FDA reports)
CEREBRAL INFARCTION ( 11 FDA reports)
INTERNATIONAL NORMALISED RATIO INCREASED ( 11 FDA reports)
JOINT STIFFNESS ( 11 FDA reports)
JOINT SWELLING ( 11 FDA reports)
ARTHRALGIA ( 10 FDA reports)
ASTHENIA ( 10 FDA reports)
CHEST DISCOMFORT ( 10 FDA reports)
DEEP VEIN THROMBOSIS ( 10 FDA reports)
DRUG INEFFECTIVE ( 10 FDA reports)
LUNG INFECTION ( 10 FDA reports)
MYOCARDIAL INFARCTION ( 10 FDA reports)
PALPITATIONS ( 10 FDA reports)
PRURITUS ( 10 FDA reports)
PULMONARY HAEMORRHAGE ( 10 FDA reports)
SCAR ( 10 FDA reports)
SKIN FIBROSIS ( 10 FDA reports)
ABASIA ( 9 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 9 FDA reports)
CEREBROVASCULAR ACCIDENT ( 9 FDA reports)
DEPRESSION ( 9 FDA reports)
FALL ( 9 FDA reports)
HYPERTENSION ( 9 FDA reports)
ISCHAEMIC STROKE ( 9 FDA reports)
SKIN HYPERPIGMENTATION ( 9 FDA reports)
THROMBOCYTOPENIA ( 9 FDA reports)
ACUTE MYOCARDIAL INFARCTION ( 8 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 8 FDA reports)
APHASIA ( 8 FDA reports)
BURNING SENSATION ( 8 FDA reports)
HAEMORRHAGE ( 8 FDA reports)
INSOMNIA ( 8 FDA reports)
NEUTROPENIA ( 8 FDA reports)
SYNCOPE ( 8 FDA reports)
ABDOMINAL DISCOMFORT ( 7 FDA reports)
BLOOD GLUCOSE INCREASED ( 7 FDA reports)
DIALYSIS ( 7 FDA reports)
DISCOMFORT ( 7 FDA reports)
FEELING ABNORMAL ( 7 FDA reports)
MEMORY IMPAIRMENT ( 7 FDA reports)
VISUAL IMPAIRMENT ( 7 FDA reports)
BACK PAIN ( 6 FDA reports)
CATARACT ( 6 FDA reports)
DISEASE PROGRESSION ( 6 FDA reports)
DRUG INTERACTION ( 6 FDA reports)
GASTRITIS EROSIVE ( 6 FDA reports)
HYPOAESTHESIA ( 6 FDA reports)
INFECTION ( 6 FDA reports)
INJURY ( 6 FDA reports)
IRRITABLE BOWEL SYNDROME ( 6 FDA reports)
LOSS OF CONSCIOUSNESS ( 6 FDA reports)
NECK PAIN ( 6 FDA reports)
PLEURAL EFFUSION ( 6 FDA reports)
RASH ( 6 FDA reports)
SKIN BURNING SENSATION ( 6 FDA reports)
SUICIDAL IDEATION ( 6 FDA reports)
ABDOMINAL PAIN UPPER ( 5 FDA reports)
AGRAPHIA ( 5 FDA reports)
ALOPECIA ( 5 FDA reports)
ANHEDONIA ( 5 FDA reports)
BLOOD CREATININE INCREASED ( 5 FDA reports)
BLOOD PRESSURE DECREASED ( 5 FDA reports)
CEREBRAL HAEMORRHAGE ( 5 FDA reports)
COGNITIVE DISORDER ( 5 FDA reports)
CONVULSION ( 5 FDA reports)
CYSTITIS ( 5 FDA reports)
DRY SKIN ( 5 FDA reports)
ERYTHEMA ( 5 FDA reports)
FIBROSIS ( 5 FDA reports)
HAEMORRHAGE INTRACRANIAL ( 5 FDA reports)
HALLUCINATION ( 5 FDA reports)
HEART RATE INCREASED ( 5 FDA reports)
HYPOGLYCAEMIA ( 5 FDA reports)
IRON DEFICIENCY ANAEMIA ( 5 FDA reports)
JOINT INSTABILITY ( 5 FDA reports)
JOINT RANGE OF MOTION DECREASED ( 5 FDA reports)
LEARNING DISORDER ( 5 FDA reports)
LIVEDO RETICULARIS ( 5 FDA reports)
MUSCULOSKELETAL CHEST PAIN ( 5 FDA reports)
PEAU D'ORANGE ( 5 FDA reports)
PERFORMANCE STATUS DECREASED ( 5 FDA reports)
PULMONARY ARTERIAL HYPERTENSION ( 5 FDA reports)
SCAB ( 5 FDA reports)
SKIN DISORDER ( 5 FDA reports)
SKIN SWELLING ( 5 FDA reports)
SKIN TIGHTNESS ( 5 FDA reports)
SKIN ULCER ( 5 FDA reports)
URINARY TRACT INFECTION ( 5 FDA reports)
WEIGHT DECREASED ( 5 FDA reports)
ABNORMAL BEHAVIOUR ( 4 FDA reports)
ADRENAL INSUFFICIENCY ( 4 FDA reports)
BLOOD POTASSIUM DECREASED ( 4 FDA reports)
BLOOD URINE PRESENT ( 4 FDA reports)
BONE PAIN ( 4 FDA reports)
BRAIN OEDEMA ( 4 FDA reports)
CANDIDIASIS ( 4 FDA reports)
CONTUSION ( 4 FDA reports)
DEFORMITY ( 4 FDA reports)
DYSGEUSIA ( 4 FDA reports)
DYSPNOEA EXERTIONAL ( 4 FDA reports)
EMBOLIC STROKE ( 4 FDA reports)
HAEMORRHOIDAL HAEMORRHAGE ( 4 FDA reports)
HYPERSOMNIA ( 4 FDA reports)
JOINT ARTHROPLASTY ( 4 FDA reports)
MALAISE ( 4 FDA reports)
MALNUTRITION ( 4 FDA reports)
METASTASES TO CENTRAL NERVOUS SYSTEM ( 4 FDA reports)
METASTASES TO LUNG ( 4 FDA reports)
MULTIPLE MYELOMA ( 4 FDA reports)
MUSCLE ATROPHY ( 4 FDA reports)
NERVE INJURY ( 4 FDA reports)
OVERDOSE ( 4 FDA reports)
OXYGEN SATURATION DECREASED ( 4 FDA reports)
PAIN OF SKIN ( 4 FDA reports)
POOR QUALITY SLEEP ( 4 FDA reports)
RASH PAPULAR ( 4 FDA reports)
RASH PRURITIC ( 4 FDA reports)
RENAL INJURY ( 4 FDA reports)
RESPIRATORY FAILURE ( 4 FDA reports)
RHABDOMYOLYSIS ( 4 FDA reports)
RIGHT VENTRICULAR FAILURE ( 4 FDA reports)
SKIN EXFOLIATION ( 4 FDA reports)
SKIN WARM ( 4 FDA reports)
SOMNOLENCE ( 4 FDA reports)
SUDDEN DEATH ( 4 FDA reports)
THROMBOANGIITIS OBLITERANS ( 4 FDA reports)
VISION BLURRED ( 4 FDA reports)
ABDOMINAL WALL HAEMORRHAGE ( 3 FDA reports)
ACUTE RESPIRATORY DISTRESS SYNDROME ( 3 FDA reports)
ANURIA ( 3 FDA reports)
BLEEDING VARICOSE VEIN ( 3 FDA reports)
BLEPHAROSPASM ( 3 FDA reports)
C-REACTIVE PROTEIN INCREASED ( 3 FDA reports)
CARDIAC DISORDER ( 3 FDA reports)
CARDIOGENIC SHOCK ( 3 FDA reports)
CARDIOMEGALY ( 3 FDA reports)
CHILLS ( 3 FDA reports)
COLON CANCER ( 3 FDA reports)
COMMUNICATION DISORDER ( 3 FDA reports)
CONDITION AGGRAVATED ( 3 FDA reports)
DEVICE RELATED SEPSIS ( 3 FDA reports)
DIARRHOEA ( 3 FDA reports)
DRY THROAT ( 3 FDA reports)
EPILEPSY ( 3 FDA reports)
EXPIRED DRUG ADMINISTERED ( 3 FDA reports)
EYE PAIN ( 3 FDA reports)
FEBRILE BONE MARROW APLASIA ( 3 FDA reports)
FEELING HOT ( 3 FDA reports)
GAIT DISTURBANCE ( 3 FDA reports)
GAMMA-GLUTAMYLTRANSFERASE INCREASED ( 3 FDA reports)
HERNIA ( 3 FDA reports)
HYPERAESTHESIA ( 3 FDA reports)
HYPERTONIC BLADDER ( 3 FDA reports)
ILL-DEFINED DISORDER ( 3 FDA reports)
JAUNDICE ( 3 FDA reports)
LARGE INTESTINE CARCINOMA ( 3 FDA reports)
LUNG ADENOCARCINOMA STAGE IV ( 3 FDA reports)
MICROCYTIC ANAEMIA ( 3 FDA reports)
MOOD ALTERED ( 3 FDA reports)
MOTOR DYSFUNCTION ( 3 FDA reports)
MULTIPLE SCLEROSIS ( 3 FDA reports)
MUSCLE SPASMS ( 3 FDA reports)
MUSCULOSKELETAL STIFFNESS ( 3 FDA reports)
NASOPHARYNGITIS ( 3 FDA reports)
NEOPLASM ( 3 FDA reports)
NYSTAGMUS ( 3 FDA reports)
ORAL DISCOMFORT ( 3 FDA reports)
ORGANISING PNEUMONIA ( 3 FDA reports)
OROPHARYNGEAL PAIN ( 3 FDA reports)
PARAESTHESIA ( 3 FDA reports)
PERSONALITY CHANGE ( 3 FDA reports)
PROTHROMBIN TIME PROLONGED ( 3 FDA reports)
RASH GENERALISED ( 3 FDA reports)
RECTAL HAEMORRHAGE ( 3 FDA reports)
SEPTIC SHOCK ( 3 FDA reports)
STRESS ( 3 FDA reports)
SUBARACHNOID HAEMORRHAGE ( 3 FDA reports)
THROAT IRRITATION ( 3 FDA reports)
THROMBOSIS ( 3 FDA reports)
TINNITUS ( 3 FDA reports)
TREMOR ( 3 FDA reports)
TUBULOINTERSTITIAL NEPHRITIS ( 3 FDA reports)
URINARY RETENTION ( 3 FDA reports)
VENOUS INSUFFICIENCY ( 3 FDA reports)
VENOUS STENOSIS ( 3 FDA reports)
VIOLENCE-RELATED SYMPTOM ( 3 FDA reports)
WEIGHT INCREASED ( 3 FDA reports)
WRONG TECHNIQUE IN DRUG USAGE PROCESS ( 3 FDA reports)
ABDOMINAL PAIN ( 2 FDA reports)
ANGINA PECTORIS ( 2 FDA reports)
ASPHYXIA ( 2 FDA reports)
BALANCE DISORDER ( 2 FDA reports)
BLINDNESS UNILATERAL ( 2 FDA reports)
BLOOD ALKALINE PHOSPHATASE INCREASED ( 2 FDA reports)
BLOOD CREATININE ABNORMAL ( 2 FDA reports)
BLOOD POTASSIUM INCREASED ( 2 FDA reports)
BLOOD PRESSURE ABNORMAL ( 2 FDA reports)
BLOOD PRESSURE INCREASED ( 2 FDA reports)
BRADYCARDIA ( 2 FDA reports)
BRAIN INJURY ( 2 FDA reports)
CARDIOVASCULAR DISORDER ( 2 FDA reports)
CENTRAL NERVOUS SYSTEM LESION ( 2 FDA reports)
CEREBRAL ISCHAEMIA ( 2 FDA reports)
CHOLELITHIASIS ( 2 FDA reports)
COAGULOPATHY ( 2 FDA reports)
COLITIS COLLAGENOUS ( 2 FDA reports)
CONSTIPATION ( 2 FDA reports)
CORONARY ARTERIAL STENT INSERTION ( 2 FDA reports)
CYSTITIS HAEMORRHAGIC ( 2 FDA reports)
CYTOLYTIC HEPATITIS ( 2 FDA reports)
DECREASED APPETITE ( 2 FDA reports)
DEHYDRATION ( 2 FDA reports)
DEPRESSED LEVEL OF CONSCIOUSNESS ( 2 FDA reports)
DISEASE RECURRENCE ( 2 FDA reports)
DRUG ERUPTION ( 2 FDA reports)
ENDOCARDITIS ( 2 FDA reports)
EPISTAXIS ( 2 FDA reports)
FEBRILE NEUTROPENIA ( 2 FDA reports)
FLANK PAIN ( 2 FDA reports)
GASTROINTESTINAL TELANGIECTASIA ( 2 FDA reports)
HAEMATOMA ( 2 FDA reports)
HAEMATURIA ( 2 FDA reports)
HEARING IMPAIRED ( 2 FDA reports)
HEPATIC FUNCTION ABNORMAL ( 2 FDA reports)
HEPATIC NECROSIS ( 2 FDA reports)
HEPATITIS TOXIC ( 2 FDA reports)
HEPATOMEGALY ( 2 FDA reports)
HEPATOTOXICITY ( 2 FDA reports)
HYPERCOAGULATION ( 2 FDA reports)
HYPERKALAEMIA ( 2 FDA reports)
HYPOACUSIS ( 2 FDA reports)
INCORRECT DOSE ADMINISTERED ( 2 FDA reports)
INJECTION SITE HAEMATOMA ( 2 FDA reports)
INJECTION SITE HAEMORRHAGE ( 2 FDA reports)
INTERNATIONAL NORMALISED RATIO FLUCTUATION ( 2 FDA reports)
INTERSTITIAL LUNG DISEASE ( 2 FDA reports)
LIVER FUNCTION TEST ABNORMAL ( 2 FDA reports)
MUSCLE SWELLING ( 2 FDA reports)
MYOCARDIAL RUPTURE ( 2 FDA reports)
NASAL CONGESTION ( 2 FDA reports)
NECROTISING FASCIITIS ( 2 FDA reports)
NEOPLASM MALIGNANT ( 2 FDA reports)
OCULAR VASCULAR DISORDER ( 2 FDA reports)
OFF LABEL USE ( 2 FDA reports)
PARESIS ( 2 FDA reports)
PNEUMONIA ASPIRATION ( 2 FDA reports)
PNEUMONIA BACTERIAL ( 2 FDA reports)
POST PROCEDURAL HAEMORRHAGE ( 2 FDA reports)
PULMONARY HYPERTENSION ( 2 FDA reports)
PULMONARY INFARCTION ( 2 FDA reports)
RENAL IMPAIRMENT ( 2 FDA reports)
RESTLESS LEGS SYNDROME ( 2 FDA reports)
SKIN DISCOLOURATION ( 2 FDA reports)
TACHYCARDIA ( 2 FDA reports)
TRANSITIONAL CELL CARCINOMA ( 2 FDA reports)
WHITE BLOOD CELL COUNT DECREASED ( 2 FDA reports)
ABNORMAL DREAMS ( 1 FDA reports)
ACCIDENTAL OVERDOSE ( 1 FDA reports)
ACUTE HEPATIC FAILURE ( 1 FDA reports)
ACUTE MYELOID LEUKAEMIA ( 1 FDA reports)
AGITATION ( 1 FDA reports)
ALTERED STATE OF CONSCIOUSNESS ( 1 FDA reports)
AMAUROSIS FUGAX ( 1 FDA reports)
ANTICOAGULATION DRUG LEVEL ABOVE THERAPEUTIC ( 1 FDA reports)
APPENDICITIS ( 1 FDA reports)
ARRHYTHMIA ( 1 FDA reports)
ARTERY DISSECTION ( 1 FDA reports)
ASTHMA ( 1 FDA reports)
AZOTAEMIA ( 1 FDA reports)
BILIARY COLIC ( 1 FDA reports)
BLOOD BILIRUBIN INCREASED ( 1 FDA reports)
BLOOD GLUCOSE DECREASED ( 1 FDA reports)
BLOOD GLUCOSE FLUCTUATION ( 1 FDA reports)
BLOOD PH INCREASED ( 1 FDA reports)
BLOOD PRESSURE IMMEASURABLE ( 1 FDA reports)
BLOOD SODIUM DECREASED ( 1 FDA reports)
BLOOD TRIGLYCERIDES INCREASED ( 1 FDA reports)
BRADYARRHYTHMIA ( 1 FDA reports)
BRONCHITIS ( 1 FDA reports)
BUNDLE BRANCH BLOCK RIGHT ( 1 FDA reports)
CACHEXIA ( 1 FDA reports)
CARDIAC ARREST ( 1 FDA reports)
CARDIAC DEATH ( 1 FDA reports)
CARDIAC FAILURE CHRONIC ( 1 FDA reports)
CARDIOACTIVE DRUG LEVEL INCREASED ( 1 FDA reports)
CATHETER RELATED INFECTION ( 1 FDA reports)
CATHETER THROMBOSIS ( 1 FDA reports)
CEREBELLAR HAEMATOMA ( 1 FDA reports)
CEREBRAL VENOUS THROMBOSIS ( 1 FDA reports)
CHOLECYSTECTOMY ( 1 FDA reports)
CHOLECYSTITIS CHRONIC ( 1 FDA reports)
CHOLURIA ( 1 FDA reports)
CHRONIC OBSTRUCTIVE PULMONARY DISEASE ( 1 FDA reports)
CLOSTRIDIAL INFECTION ( 1 FDA reports)
COAGULATION TEST ABNORMAL ( 1 FDA reports)
COAGULATION TIME PROLONGED ( 1 FDA reports)
COLON NEOPLASM ( 1 FDA reports)
COMPARTMENT SYNDROME ( 1 FDA reports)
CONFUSIONAL STATE ( 1 FDA reports)
CONGESTIVE CARDIOMYOPATHY ( 1 FDA reports)
COOMBS POSITIVE HAEMOLYTIC ANAEMIA ( 1 FDA reports)
CORONARY ARTERY DISEASE ( 1 FDA reports)
CRYING ( 1 FDA reports)
CYANOSIS ( 1 FDA reports)
DIABETES MELLITUS ( 1 FDA reports)
DIABETES MELLITUS INADEQUATE CONTROL ( 1 FDA reports)
DILATATION VENTRICULAR ( 1 FDA reports)
DISORIENTATION ( 1 FDA reports)
DISSEMINATED INTRAVASCULAR COAGULATION ( 1 FDA reports)
DIZZINESS POSTURAL ( 1 FDA reports)
DRUG EXPOSURE BEFORE PREGNANCY ( 1 FDA reports)
DRUG EXPOSURE DURING PREGNANCY ( 1 FDA reports)
DRUG LEVEL DECREASED ( 1 FDA reports)
DRUG WITHDRAWAL SYNDROME ( 1 FDA reports)
DYSARTHRIA ( 1 FDA reports)
DYSLIPIDAEMIA ( 1 FDA reports)
DYSSTASIA ( 1 FDA reports)
EAR PAIN ( 1 FDA reports)
ECCHYMOSIS ( 1 FDA reports)
ELECTROENCEPHALOGRAM ABNORMAL ( 1 FDA reports)
EXCORIATION ( 1 FDA reports)
EXTREMITY NECROSIS ( 1 FDA reports)
FACE OEDEMA ( 1 FDA reports)
FACIAL PALSY ( 1 FDA reports)
FAECES DISCOLOURED ( 1 FDA reports)
FEAR ( 1 FDA reports)
FISTULA ( 1 FDA reports)
FLATULENCE ( 1 FDA reports)
FLUSHING ( 1 FDA reports)
GALLBLADDER DISORDER ( 1 FDA reports)
GANGRENE ( 1 FDA reports)
GAS POISONING ( 1 FDA reports)
GASTRITIS ( 1 FDA reports)
GESTATIONAL DIABETES ( 1 FDA reports)
GINGIVITIS ( 1 FDA reports)
GLYCOSYLATED HAEMOGLOBIN INCREASED ( 1 FDA reports)
HAEMATEMESIS ( 1 FDA reports)
HAEMATOCRIT DECREASED ( 1 FDA reports)
HAEMODIALYSIS ( 1 FDA reports)
HAEMOLYTIC ANAEMIA ( 1 FDA reports)
HAEMORRHAGIC ANAEMIA ( 1 FDA reports)
HAEMORRHAGIC CEREBRAL INFARCTION ( 1 FDA reports)
HAEMORRHAGIC EROSIVE GASTRITIS ( 1 FDA reports)
HAEMORRHOIDS ( 1 FDA reports)
HEMIPARESIS ( 1 FDA reports)
HEMIPLEGIA ( 1 FDA reports)
HEPATIC FAILURE ( 1 FDA reports)
HEPATIC FIBROSIS ( 1 FDA reports)
HEPATITIS ( 1 FDA reports)
HEPATOJUGULAR REFLUX ( 1 FDA reports)
HIGH DENSITY LIPOPROTEIN DECREASED ( 1 FDA reports)
HYPERGLYCAEMIA ( 1 FDA reports)
HYPERHIDROSIS ( 1 FDA reports)
HYPERSENSITIVITY ( 1 FDA reports)
HYPOCALCAEMIA ( 1 FDA reports)
HYPOTHYROIDISM ( 1 FDA reports)
INCORRECT DRUG ADMINISTRATION DURATION ( 1 FDA reports)
INCORRECT DRUG ADMINISTRATION RATE ( 1 FDA reports)
INCREASED APPETITE ( 1 FDA reports)
INJECTION SITE PAIN ( 1 FDA reports)
INTERMITTENT CLAUDICATION ( 1 FDA reports)
INTERNATIONAL NORMALISED RATIO ABNORMAL ( 1 FDA reports)
INTESTINAL HAEMORRHAGE ( 1 FDA reports)
LABORATORY TEST ABNORMAL ( 1 FDA reports)
LACUNAR INFARCTION ( 1 FDA reports)
LETHARGY ( 1 FDA reports)
LIVER DISORDER ( 1 FDA reports)
LOWER GASTROINTESTINAL HAEMORRHAGE ( 1 FDA reports)
LUNG DISORDER ( 1 FDA reports)
LUNG INFECTION PSEUDOMONAL ( 1 FDA reports)
MACULAR DEGENERATION ( 1 FDA reports)
MEDICAL DEVICE COMPLICATION ( 1 FDA reports)
MEDICATION ERROR ( 1 FDA reports)
MENINGITIS ( 1 FDA reports)
MENOMETRORRHAGIA ( 1 FDA reports)
MENORRHAGIA ( 1 FDA reports)
MENTAL DISORDER ( 1 FDA reports)
MENTAL IMPAIRMENT ( 1 FDA reports)
MENTAL STATUS CHANGES ( 1 FDA reports)
METASTASES TO HEART ( 1 FDA reports)
METASTATIC RENAL CELL CARCINOMA ( 1 FDA reports)
MOUTH HAEMORRHAGE ( 1 FDA reports)
MUSCLE CONTRACTURE ( 1 FDA reports)
MUSCLE HAEMORRHAGE ( 1 FDA reports)
MUSCLE TIGHTNESS ( 1 FDA reports)
MUSCULOSKELETAL DISORDER ( 1 FDA reports)
MYELODYSPLASTIC SYNDROME TRANSFORMATION ( 1 FDA reports)
MYOCARDIAL ISCHAEMIA ( 1 FDA reports)
NEPHROTIC SYNDROME ( 1 FDA reports)
NIGHT BLINDNESS ( 1 FDA reports)
NIGHT SWEATS ( 1 FDA reports)
NUTRITIONAL CONDITION ABNORMAL ( 1 FDA reports)
OEDEMA ( 1 FDA reports)
OPERATIVE HAEMORRHAGE ( 1 FDA reports)
OPPORTUNISTIC INFECTION ( 1 FDA reports)
PALMAR-PLANTAR ERYTHRODYSAESTHESIA SYNDROME ( 1 FDA reports)
PANCREATIC CARCINOMA ( 1 FDA reports)
PANCREATITIS ( 1 FDA reports)
PARALYSIS ( 1 FDA reports)
PARANOIA ( 1 FDA reports)
PARAPARESIS ( 1 FDA reports)
PERICARDIAL EFFUSION ( 1 FDA reports)
PERICARDITIS ( 1 FDA reports)
PHANTOM PAIN ( 1 FDA reports)
PLEURITIC PAIN ( 1 FDA reports)
PLEUROPERICARDITIS ( 1 FDA reports)
PNEUMONIA STAPHYLOCOCCAL ( 1 FDA reports)
PO2 DECREASED ( 1 FDA reports)
POST PROCEDURAL COMPLICATION ( 1 FDA reports)
POSTERIOR CAPSULE OPACIFICATION ( 1 FDA reports)
PREGNANCY ( 1 FDA reports)
PREGNANCY WITH CONTRACEPTIVE DEVICE ( 1 FDA reports)
PRODUCTIVE COUGH ( 1 FDA reports)
PROSTATE CANCER ( 1 FDA reports)
PROTHROMBIN TIME ABNORMAL ( 1 FDA reports)
PSEUDOMONAL SEPSIS ( 1 FDA reports)
PULMONARY ARTERIAL PRESSURE ABNORMAL ( 1 FDA reports)
PULMONARY ARTERIAL PRESSURE INCREASED ( 1 FDA reports)
PULMONARY ARTERY THROMBOSIS ( 1 FDA reports)
PULMONARY CAVITATION ( 1 FDA reports)
PULMONARY CONGESTION ( 1 FDA reports)
PULMONARY THROMBOSIS ( 1 FDA reports)
QRS AXIS ABNORMAL ( 1 FDA reports)
QUALITY OF LIFE DECREASED ( 1 FDA reports)
RADIATION INJURY ( 1 FDA reports)
RALES ( 1 FDA reports)
RASH MACULAR ( 1 FDA reports)
RED BLOOD CELL COUNT DECREASED ( 1 FDA reports)
RED BLOOD CELL SEDIMENTATION RATE INCREASED ( 1 FDA reports)
RESPIRATORY DISORDER ( 1 FDA reports)
RESPIRATORY RATE INCREASED ( 1 FDA reports)
RESTRICTIVE CARDIOMYOPATHY ( 1 FDA reports)
RETINAL ISCHAEMIA ( 1 FDA reports)
RETINOPATHY ( 1 FDA reports)
RIGHT VENTRICULAR HYPERTROPHY ( 1 FDA reports)
SENSORY LOSS ( 1 FDA reports)
SERUM FERRITIN INCREASED ( 1 FDA reports)
SHOCK ( 1 FDA reports)
SIGMOIDITIS ( 1 FDA reports)
SINUSITIS ( 1 FDA reports)
SKIN OEDEMA ( 1 FDA reports)
SKIN PAPILLOMA ( 1 FDA reports)
SKIN TOXICITY ( 1 FDA reports)
SLEEP DISORDER ( 1 FDA reports)
SPEECH DISORDER ( 1 FDA reports)
SPINAL CORD INFARCTION ( 1 FDA reports)
STAPHYLOCOCCAL INFECTION ( 1 FDA reports)
SUBDURAL HAEMORRHAGE ( 1 FDA reports)
SUDDEN CARDIAC DEATH ( 1 FDA reports)
SUPRAVENTRICULAR TACHYCARDIA ( 1 FDA reports)
SWELLING ( 1 FDA reports)
SWELLING FACE ( 1 FDA reports)
THALAMUS HAEMORRHAGE ( 1 FDA reports)
THROMBOPHLEBITIS ( 1 FDA reports)
THROMBOPHLEBITIS SUPERFICIAL ( 1 FDA reports)
THROMBOSIS IN DEVICE ( 1 FDA reports)
THROMBOTIC CEREBRAL INFARCTION ( 1 FDA reports)
THYROIDITIS ( 1 FDA reports)
TOE AMPUTATION ( 1 FDA reports)
TORTICOLLIS ( 1 FDA reports)
TRANSAMINASES INCREASED ( 1 FDA reports)
TRAUMATIC BRAIN INJURY ( 1 FDA reports)
URTICARIA ( 1 FDA reports)
VASCULAR FRAGILITY ( 1 FDA reports)
VULVOVAGINAL MYCOTIC INFECTION ( 1 FDA reports)
VULVOVAGINAL PAIN ( 1 FDA reports)
WHOLE BLOOD TRANSFUSION ( 1 FDA reports)
WOUND HAEMORRHAGE ( 1 FDA reports)
WOUND SECRETION ( 1 FDA reports)

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