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

PYREXIA ( 34 FDA reports)
ALTERED STATE OF CONSCIOUSNESS ( 27 FDA reports)
ANAEMIA ( 26 FDA reports)
INTERSTITIAL LUNG DISEASE ( 26 FDA reports)
CEREBRAL INFARCTION ( 25 FDA reports)
RENAL IMPAIRMENT ( 25 FDA reports)
DISSEMINATED INTRAVASCULAR COAGULATION ( 23 FDA reports)
PLATELET COUNT DECREASED ( 23 FDA reports)
WHITE BLOOD CELL COUNT DECREASED ( 23 FDA reports)
PNEUMONIA ( 17 FDA reports)
VOMITING ( 16 FDA reports)
BLOOD PHOSPHORUS DECREASED ( 15 FDA reports)
HYPONATRAEMIA ( 15 FDA reports)
LUMBAR SPINAL STENOSIS ( 15 FDA reports)
BLOOD LACTATE DEHYDROGENASE INCREASED ( 14 FDA reports)
BLOOD POTASSIUM DECREASED ( 14 FDA reports)
BRADYCARDIA ( 14 FDA reports)
CONVULSION ( 14 FDA reports)
DIARRHOEA ( 13 FDA reports)
TINNITUS ( 13 FDA reports)
URINARY TRACT INFECTION ( 13 FDA reports)
WHITE BLOOD CELL COUNT INCREASED ( 13 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 12 FDA reports)
BLOOD ALKALINE PHOSPHATASE INCREASED ( 12 FDA reports)
HEADACHE ( 12 FDA reports)
HEPATIC FUNCTION ABNORMAL ( 12 FDA reports)
NAUSEA ( 12 FDA reports)
RENAL FAILURE ACUTE ( 12 FDA reports)
THROMBOCYTOPENIA ( 12 FDA reports)
LOSS OF CONSCIOUSNESS ( 11 FDA reports)
RETINAL HAEMORRHAGE ( 11 FDA reports)
ACUTE DISSEMINATED ENCEPHALOMYELITIS ( 10 FDA reports)
BLOOD CREATININE INCREASED ( 10 FDA reports)
BLOOD UREA INCREASED ( 10 FDA reports)
C-REACTIVE PROTEIN INCREASED ( 10 FDA reports)
DEAFNESS BILATERAL ( 10 FDA reports)
LIVER DISORDER ( 10 FDA reports)
MUSCULAR WEAKNESS ( 10 FDA reports)
OVERDOSE ( 10 FDA reports)
PNEUMOCYSTIS JIROVECI PNEUMONIA ( 10 FDA reports)
TEMPERATURE INTOLERANCE ( 10 FDA reports)
BLOOD PRESSURE DECREASED ( 9 FDA reports)
HYPOTENSION ( 9 FDA reports)
LYMPHOCYTE COUNT DECREASED ( 9 FDA reports)
SEPSIS ( 9 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 8 FDA reports)
BLOOD AMYLASE INCREASED ( 8 FDA reports)
CONSTIPATION ( 8 FDA reports)
DEATH ( 8 FDA reports)
DECREASED APPETITE ( 8 FDA reports)
JOINT SWELLING ( 8 FDA reports)
MACULAR OEDEMA ( 8 FDA reports)
MALAISE ( 8 FDA reports)
SOMNOLENCE ( 8 FDA reports)
CIRCULATORY COLLAPSE ( 7 FDA reports)
DEEP VEIN THROMBOSIS ( 7 FDA reports)
DYSPHAGIA ( 7 FDA reports)
DYSPNOEA EXERTIONAL ( 7 FDA reports)
HAEMOGLOBIN DECREASED ( 7 FDA reports)
HYPERTENSION ( 7 FDA reports)
HYPOCALCAEMIA ( 7 FDA reports)
LIPASE INCREASED ( 7 FDA reports)
LYMPHOMA ( 7 FDA reports)
RED BLOOD CELL COUNT DECREASED ( 7 FDA reports)
URINE OUTPUT DECREASED ( 7 FDA reports)
VASCULITIS ( 7 FDA reports)
CARDIAC ARREST ( 6 FDA reports)
CARDIAC FAILURE ( 6 FDA reports)
CARDIO-RESPIRATORY ARREST ( 6 FDA reports)
CHEST PAIN ( 6 FDA reports)
COMA ( 6 FDA reports)
COMMUNICATION DISORDER ( 6 FDA reports)
DRUG INTERACTION ( 6 FDA reports)
ECZEMA ( 6 FDA reports)
ENCEPHALOPATHY ( 6 FDA reports)
GAIT DISTURBANCE ( 6 FDA reports)
GAMMA-GLUTAMYLTRANSFERASE INCREASED ( 6 FDA reports)
GASTROENTERITIS ( 6 FDA reports)
HERPES ZOSTER ( 6 FDA reports)
HYPOPHAGIA ( 6 FDA reports)
INFUSION RELATED REACTION ( 6 FDA reports)
LACRIMATION INCREASED ( 6 FDA reports)
LARGE INTESTINAL HAEMORRHAGE ( 6 FDA reports)
MULTIPLE MYELOMA ( 6 FDA reports)
MUSCLE SPASMS ( 6 FDA reports)
NASOPHARYNGITIS ( 6 FDA reports)
NEUTROPENIA ( 6 FDA reports)
OEDEMA PERIPHERAL ( 6 FDA reports)
PANCYTOPENIA ( 6 FDA reports)
PNEUMONIA STAPHYLOCOCCAL ( 6 FDA reports)
SALIVARY HYPERSECRETION ( 6 FDA reports)
SUBARACHNOID HAEMORRHAGE ( 6 FDA reports)
THINKING ABNORMAL ( 6 FDA reports)
APPENDICITIS ( 5 FDA reports)
ASTHENIA ( 5 FDA reports)
BLOOD BILIRUBIN INCREASED ( 5 FDA reports)
CATHETER PLACEMENT ( 5 FDA reports)
CATHETER RELATED INFECTION ( 5 FDA reports)
CATHETER REMOVAL ( 5 FDA reports)
CEREBRAL ISCHAEMIA ( 5 FDA reports)
CONJUNCTIVITIS ( 5 FDA reports)
HYPERGLYCAEMIA ( 5 FDA reports)
LUNG INFILTRATION ( 5 FDA reports)
MUSCLE CONTRACTURE ( 5 FDA reports)
MYCOBACTERIUM AVIUM COMPLEX INFECTION ( 5 FDA reports)
MYOCLONUS ( 5 FDA reports)
NEOPLASM MALIGNANT ( 5 FDA reports)
OVARIAN CANCER RECURRENT ( 5 FDA reports)
PALPITATIONS ( 5 FDA reports)
PARKINSONISM ( 5 FDA reports)
PLEURAL EFFUSION ( 5 FDA reports)
RENAL DISORDER ( 5 FDA reports)
RESPIRATORY DISTRESS ( 5 FDA reports)
RESPIRATORY TRACT INFECTION ( 5 FDA reports)
STAPHYLOCOCCAL INFECTION ( 5 FDA reports)
URTICARIA ( 5 FDA reports)
ABDOMINAL PAIN ( 4 FDA reports)
ABDOMINAL PAIN UPPER ( 4 FDA reports)
ADRENAL INSUFFICIENCY ( 4 FDA reports)
ANAPHYLACTIC SHOCK ( 4 FDA reports)
ARTHRALGIA ( 4 FDA reports)
ASCITES ( 4 FDA reports)
BLOOD ALBUMIN DECREASED ( 4 FDA reports)
BLOOD PRESSURE INCREASED ( 4 FDA reports)
BRAIN STEM SYNDROME ( 4 FDA reports)
BREAST CANCER ( 4 FDA reports)
CELLULITIS ( 4 FDA reports)
CONDITION AGGRAVATED ( 4 FDA reports)
COUGH ( 4 FDA reports)
DELIRIUM ( 4 FDA reports)
DIZZINESS ( 4 FDA reports)
DYSPEPSIA ( 4 FDA reports)
DYSPNOEA ( 4 FDA reports)
EOSINOPHIL COUNT INCREASED ( 4 FDA reports)
ERYTHEMA ( 4 FDA reports)
FALL ( 4 FDA reports)
GENERAL PHYSICAL HEALTH DETERIORATION ( 4 FDA reports)
HAEMATOCRIT DECREASED ( 4 FDA reports)
HAEMATURIA ( 4 FDA reports)
HAEMOPTYSIS ( 4 FDA reports)
MALIGNANT NEOPLASM PROGRESSION ( 4 FDA reports)
NEPHROTIC SYNDROME ( 4 FDA reports)
OXYGEN SATURATION DECREASED ( 4 FDA reports)
PANCREATIC ENZYMES INCREASED ( 4 FDA reports)
PNEUMOTHORAX ( 4 FDA reports)
PULMONARY ARTERY THROMBOSIS ( 4 FDA reports)
PULMONARY EMBOLISM ( 4 FDA reports)
RASH ( 4 FDA reports)
RENAL FAILURE ( 4 FDA reports)
RHABDOMYOLYSIS ( 4 FDA reports)
SHOCK ( 4 FDA reports)
SHOCK HAEMORRHAGIC ( 4 FDA reports)
STOMATITIS ( 4 FDA reports)
SUBCUTANEOUS ABSCESS ( 4 FDA reports)
SUICIDE ATTEMPT ( 4 FDA reports)
URINARY RETENTION ( 4 FDA reports)
VISUAL ACUITY REDUCED ( 4 FDA reports)
WEIGHT DECREASED ( 4 FDA reports)
ABDOMINAL TENDERNESS ( 3 FDA reports)
ACUTE MYELOID LEUKAEMIA ( 3 FDA reports)
BACK PAIN ( 3 FDA reports)
BLOOD THYROID STIMULATING HORMONE INCREASED ( 3 FDA reports)
BODY TEMPERATURE DECREASED ( 3 FDA reports)
BRONCHOPULMONARY ASPERGILLOSIS ( 3 FDA reports)
C-REACTIVE PROTEIN DECREASED ( 3 FDA reports)
CENTRAL NERVOUS SYSTEM LESION ( 3 FDA reports)
CEREBRAL HAEMORRHAGE ( 3 FDA reports)
CHOKING ( 3 FDA reports)
CYST ( 3 FDA reports)
CYTOMEGALOVIRUS VIRAEMIA ( 3 FDA reports)
DEPRESSED LEVEL OF CONSCIOUSNESS ( 3 FDA reports)
DRUG INEFFECTIVE ( 3 FDA reports)
DYSPHONIA ( 3 FDA reports)
ENTEROCOCCAL SEPSIS ( 3 FDA reports)
ESCHERICHIA SEPSIS ( 3 FDA reports)
FUNGAL INFECTION ( 3 FDA reports)
GENERALISED OEDEMA ( 3 FDA reports)
GLOSSODYNIA ( 3 FDA reports)
HAEMATEMESIS ( 3 FDA reports)
HAEMATOCHEZIA ( 3 FDA reports)
HAEMOLYSIS ( 3 FDA reports)
HAEMORRHAGE SUBCUTANEOUS ( 3 FDA reports)
HYPERKALAEMIA ( 3 FDA reports)
HYPOALBUMINAEMIA ( 3 FDA reports)
HYPOGLYCAEMIA ( 3 FDA reports)
HYPOTHYROIDISM ( 3 FDA reports)
HYPOXIA ( 3 FDA reports)
ILEUS PARALYTIC ( 3 FDA reports)
INTUSSUSCEPTION ( 3 FDA reports)
JAUNDICE ( 3 FDA reports)
JEJUNAL PERFORATION ( 3 FDA reports)
LARYNGEAL GRANULOMA ( 3 FDA reports)
LUNG ABSCESS ( 3 FDA reports)
NEONATAL ASPHYXIA ( 3 FDA reports)
NERVOUS SYSTEM DISORDER ( 3 FDA reports)
NEUROGENIC BLADDER ( 3 FDA reports)
OEDEMA ( 3 FDA reports)
OLIGURIA ( 3 FDA reports)
OSTEOARTHRITIS ( 3 FDA reports)
OSTEONECROSIS OF JAW ( 3 FDA reports)
PALMAR-PLANTAR ERYTHRODYSAESTHESIA SYNDROME ( 3 FDA reports)
PANCREATITIS ( 3 FDA reports)
PANCREATITIS ACUTE ( 3 FDA reports)
PARALYSIS ( 3 FDA reports)
PLEURISY ( 3 FDA reports)
PNEUMONIA ASPIRATION ( 3 FDA reports)
PNEUMONIA BACTERIAL ( 3 FDA reports)
PSEUDOMONAS INFECTION ( 3 FDA reports)
PULMONARY OEDEMA ( 3 FDA reports)
RASH GENERALISED ( 3 FDA reports)
RESPIRATORY FAILURE ( 3 FDA reports)
SINUS BRADYCARDIA ( 3 FDA reports)
SKIN ATROPHY ( 3 FDA reports)
SYNCOPE ( 3 FDA reports)
TRAUMATIC FRACTURE ( 3 FDA reports)
TUBERCULOSIS TEST POSITIVE ( 3 FDA reports)
VASCULITIS CEREBRAL ( 3 FDA reports)
WEIGHT INCREASED ( 3 FDA reports)
WHEEZING ( 3 FDA reports)
ABDOMINAL DISCOMFORT ( 2 FDA reports)
ABDOMINAL DISTENSION ( 2 FDA reports)
ACUTE GENERALISED EXANTHEMATOUS PUSTULOSIS ( 2 FDA reports)
ACUTE RESPIRATORY DISTRESS SYNDROME ( 2 FDA reports)
AMNESIA ( 2 FDA reports)
ANOREXIA ( 2 FDA reports)
AORTIC ANEURYSM RUPTURE ( 2 FDA reports)
AORTIC DISSECTION ( 2 FDA reports)
APNOEA ( 2 FDA reports)
ARTERIOSCLEROTIC RETINOPATHY ( 2 FDA reports)
ARTHRITIS ( 2 FDA reports)
ASPIRATION ( 2 FDA reports)
ASTHMA ( 2 FDA reports)
ATELECTASIS ( 2 FDA reports)
BACTERIAL INFECTION ( 2 FDA reports)
BLADDER CATHETERISATION ( 2 FDA reports)
BLADDER TRANSITIONAL CELL CARCINOMA ( 2 FDA reports)
BLOOD CREATINE PHOSPHOKINASE INCREASED ( 2 FDA reports)
BLOOD FOLATE DECREASED ( 2 FDA reports)
BLOOD POTASSIUM INCREASED ( 2 FDA reports)
BLOOD SODIUM DECREASED ( 2 FDA reports)
BODY TEMPERATURE INCREASED ( 2 FDA reports)
BONE MARROW FAILURE ( 2 FDA reports)
BRAIN DEATH ( 2 FDA reports)
CARDIAC FAILURE CONGESTIVE ( 2 FDA reports)
CARDIAC TAMPONADE ( 2 FDA reports)
CATARACT ( 2 FDA reports)
CELLULITIS STAPHYLOCOCCAL ( 2 FDA reports)
CERVICAL DYSPLASIA ( 2 FDA reports)
CHEST X-RAY ABNORMAL ( 2 FDA reports)
CLAVICLE FRACTURE ( 2 FDA reports)
COLITIS ISCHAEMIC ( 2 FDA reports)
CYANOSIS ( 2 FDA reports)
DECREASED ACTIVITY ( 2 FDA reports)
DECUBITUS ULCER ( 2 FDA reports)
DEMENTIA ( 2 FDA reports)
DEMENTIA ALZHEIMER'S TYPE ( 2 FDA reports)
DEPRESSION ( 2 FDA reports)
DIABETES MELLITUS ( 2 FDA reports)
DISCOMFORT ( 2 FDA reports)
DISEASE PROGRESSION ( 2 FDA reports)
DISSEMINATED TUBERCULOSIS ( 2 FDA reports)
DRUG ERUPTION ( 2 FDA reports)
DYSGEUSIA ( 2 FDA reports)
DYSLALIA ( 2 FDA reports)
ELECTROCARDIOGRAM ABNORMAL ( 2 FDA reports)
EMBOLISM VENOUS ( 2 FDA reports)
ENTEROCOLITIS ( 2 FDA reports)
ENTEROCOLITIS BACTERIAL ( 2 FDA reports)
ERYTHEMA MULTIFORME ( 2 FDA reports)
FACIAL PALSY ( 2 FDA reports)
FATIGUE ( 2 FDA reports)
FEMORAL NECK FRACTURE ( 2 FDA reports)
FIBULA FRACTURE ( 2 FDA reports)
FISTULA ( 2 FDA reports)
FOAMING AT MOUTH ( 2 FDA reports)
FOREARM FRACTURE ( 2 FDA reports)
GALACTORRHOEA ( 2 FDA reports)
GASTRIC CANCER ( 2 FDA reports)
GASTRIC ULCER HAEMORRHAGE ( 2 FDA reports)
GASTROINTESTINAL HAEMORRHAGE ( 2 FDA reports)
GASTROOESOPHAGEAL REFLUX DISEASE ( 2 FDA reports)
GINGIVAL HYPERPLASIA ( 2 FDA reports)
GINGIVAL SWELLING ( 2 FDA reports)
GLOSSITIS ( 2 FDA reports)
GLYCOSYLATED HAEMOGLOBIN INCREASED ( 2 FDA reports)
HAEMATOCRIT INCREASED ( 2 FDA reports)
HEPATIC STEATOSIS ( 2 FDA reports)
HYPERNATRAEMIA ( 2 FDA reports)
HYPERVENTILATION ( 2 FDA reports)
HYPOAESTHESIA ORAL ( 2 FDA reports)
HYPOKINESIA ( 2 FDA reports)
HYPOXIC ENCEPHALOPATHY ( 2 FDA reports)
INAPPROPRIATE ANTIDIURETIC HORMONE SECRETION ( 2 FDA reports)
INJURY ASPHYXIATION ( 2 FDA reports)
INTRAOCULAR PRESSURE INCREASED ( 2 FDA reports)
JAW DISORDER ( 2 FDA reports)
JOINT WARMTH ( 2 FDA reports)
LEUKAEMIA ( 2 FDA reports)
LIGAMENT RUPTURE ( 2 FDA reports)
LUNG DISORDER ( 2 FDA reports)
MALLORY-WEISS SYNDROME ( 2 FDA reports)
MELAENA ( 2 FDA reports)
METABOLIC ENCEPHALOPATHY ( 2 FDA reports)
METASTASES TO BLADDER ( 2 FDA reports)
MULTIPLE SCLEROSIS RELAPSE ( 2 FDA reports)
MUSCULOSKELETAL CHEST PAIN ( 2 FDA reports)
MYALGIA ( 2 FDA reports)
MYELOBLAST COUNT INCREASED ( 2 FDA reports)
MYOCARDIAL ISCHAEMIA ( 2 FDA reports)
NEUTROPHIL PERCENTAGE INCREASED ( 2 FDA reports)
ORAL PUSTULE ( 2 FDA reports)
OSTEOMYELITIS ( 2 FDA reports)
OSTEOPOROSIS ( 2 FDA reports)
PALLOR ( 2 FDA reports)
PHYSIOTHERAPY ( 2 FDA reports)
PNEUMOMEDIASTINUM ( 2 FDA reports)
PNEUMONIA LEGIONELLA ( 2 FDA reports)
PNEUMONIA VIRAL ( 2 FDA reports)
POLYARTHRITIS ( 2 FDA reports)
POSTRENAL FAILURE ( 2 FDA reports)
PROTEIN TOTAL DECREASED ( 2 FDA reports)
PROTHROMBIN TIME PROLONGED ( 2 FDA reports)
PRURITUS ( 2 FDA reports)
PULMONARY HAEMORRHAGE ( 2 FDA reports)
PULMONARY TUBERCULOSIS ( 2 FDA reports)
PUSTULAR PSORIASIS ( 2 FDA reports)
PYELONEPHRITIS ( 2 FDA reports)
RASH PUSTULAR ( 2 FDA reports)
RED BLOOD CELL SEDIMENTATION RATE INCREASED ( 2 FDA reports)
RETROPERITONEAL LYMPHADENOPATHY ( 2 FDA reports)
RHEUMATOID ARTHRITIS ( 2 FDA reports)
RIB FRACTURE ( 2 FDA reports)
SEPTIC SHOCK ( 2 FDA reports)
SKIN EXFOLIATION ( 2 FDA reports)
SKIN ULCER ( 2 FDA reports)
SPEECH REHABILITATION ( 2 FDA reports)
SPINAL COMPRESSION FRACTURE ( 2 FDA reports)
SUBCUTANEOUS EMPHYSEMA ( 2 FDA reports)
SUBDURAL HAEMORRHAGE ( 2 FDA reports)
TENDON DISORDER ( 2 FDA reports)
THERAPY NON-RESPONDER ( 2 FDA reports)
TROUSSEAU'S SYNDROME ( 2 FDA reports)
TUBERCULOSIS ( 2 FDA reports)
TUBULOINTERSTITIAL NEPHRITIS ( 2 FDA reports)
UPPER RESPIRATORY TRACT INFLAMMATION ( 2 FDA reports)
VARICELLA ( 2 FDA reports)
VISION BLURRED ( 2 FDA reports)
ACUTE MYOCARDIAL INFARCTION ( 1 FDA reports)
ARRHYTHMIA ( 1 FDA reports)
ARTERIAL THROMBOSIS ( 1 FDA reports)
BACK DISORDER ( 1 FDA reports)
BACTERAEMIA ( 1 FDA reports)
BACTERIA STOOL IDENTIFIED ( 1 FDA reports)
BLADDER CANCER ( 1 FDA reports)
BLOOD CALCIUM DECREASED ( 1 FDA reports)
BLOOD GLUCOSE INCREASED ( 1 FDA reports)
BLOOD LACTATE DEHYDROGENASE DECREASED ( 1 FDA reports)
BLOOD SODIUM INCREASED ( 1 FDA reports)
BLOOD URIC ACID INCREASED ( 1 FDA reports)
BREAST ENLARGEMENT ( 1 FDA reports)
BREAST OEDEMA ( 1 FDA reports)
CANDIDA SEROLOGY POSITIVE ( 1 FDA reports)
CARDIAC FAILURE ACUTE ( 1 FDA reports)
CHOLECYSTITIS ( 1 FDA reports)
COLD SWEAT ( 1 FDA reports)
COLITIS COLLAGENOUS ( 1 FDA reports)
COMPRESSION FRACTURE ( 1 FDA reports)
CONJUNCTIVAL HAEMORRHAGE ( 1 FDA reports)
CONTINUOUS HAEMODIAFILTRATION ( 1 FDA reports)
COXSACKIE VIRAL INFECTION ( 1 FDA reports)
CRYPTOGENIC ORGANISING PNEUMONIA ( 1 FDA reports)
CYSTITIS ( 1 FDA reports)
CYSTITIS HAEMORRHAGIC ( 1 FDA reports)
DEATH NEONATAL ( 1 FDA reports)
DEHYDRATION ( 1 FDA reports)
DIABETES MELLITUS INADEQUATE CONTROL ( 1 FDA reports)
DIFFUSE LARGE B-CELL LYMPHOMA ( 1 FDA reports)
DISUSE SYNDROME ( 1 FDA reports)
DIVERTICULITIS ( 1 FDA reports)
DROWNING ( 1 FDA reports)
DRUG LEVEL INCREASED ( 1 FDA reports)
DRUG-INDUCED LIVER INJURY ( 1 FDA reports)
DYSURIA ( 1 FDA reports)
EPIDERMAL GROWTH FACTOR RECEPTOR INCREASED ( 1 FDA reports)
EXECUTIVE DYSFUNCTION ( 1 FDA reports)
EYE INJURY ( 1 FDA reports)
FAECAL INCONTINENCE ( 1 FDA reports)
FEAR OF DEATH ( 1 FDA reports)
FEELING ABNORMAL ( 1 FDA reports)
GASTRIC ULCER ( 1 FDA reports)
GLIOBLASTOMA MULTIFORME ( 1 FDA reports)
GOUT ( 1 FDA reports)
HAEMATOMA ( 1 FDA reports)
HAEMOGLOBIN INCREASED ( 1 FDA reports)
HEPATIC CIRRHOSIS ( 1 FDA reports)
HEPATIC ENCEPHALOPATHY ( 1 FDA reports)
HYPERCALCAEMIA ( 1 FDA reports)
HYPERCAPNIA ( 1 FDA reports)
HYPERLIPIDAEMIA ( 1 FDA reports)
HYPERSENSITIVITY ( 1 FDA reports)
HYPERURICAEMIA ( 1 FDA reports)
HYPOCAPNIA ( 1 FDA reports)
HYPOGLYCAEMIC COMA ( 1 FDA reports)
HYPOKALAEMIA ( 1 FDA reports)
HYPOPROTEINAEMIA ( 1 FDA reports)
HYPOTHERMIA ( 1 FDA reports)
HYSTERECTOMY ( 1 FDA reports)
INFECTION IN AN IMMUNOCOMPROMISED HOST ( 1 FDA reports)
INFLAMMATORY CARCINOMA OF THE BREAST ( 1 FDA reports)
INFLUENZA ( 1 FDA reports)
INSOMNIA ( 1 FDA reports)
INTESTINAL HAEMATOMA ( 1 FDA reports)
INTESTINAL PERFORATION ( 1 FDA reports)
INTRACRANIAL ANEURYSM ( 1 FDA reports)
INTRAUTERINE INFECTION ( 1 FDA reports)
JAUNDICE CHOLESTATIC ( 1 FDA reports)
LABORATORY TEST ABNORMAL ( 1 FDA reports)
LACUNAR INFARCTION ( 1 FDA reports)
LEUKOPENIA ( 1 FDA reports)
LISTLESS ( 1 FDA reports)
LIVER FUNCTION TEST ABNORMAL ( 1 FDA reports)
LUNG NEOPLASM ( 1 FDA reports)
LUNG NEOPLASM MALIGNANT ( 1 FDA reports)
LUNG SQUAMOUS CELL CARCINOMA STAGE UNSPECIFIED ( 1 FDA reports)
LYMPHADENOPATHY ( 1 FDA reports)
MALABSORPTION ( 1 FDA reports)
MALIGNANT PLEURAL EFFUSION ( 1 FDA reports)
MEDICATION ERROR ( 1 FDA reports)
METASTASES TO LYMPH NODES ( 1 FDA reports)
MIXED DEAFNESS ( 1 FDA reports)
MULTI-ORGAN FAILURE ( 1 FDA reports)
NECK PAIN ( 1 FDA reports)
NEOPLASM ( 1 FDA reports)
NEOPLASM PROGRESSION ( 1 FDA reports)
NEUTROPHIL COUNT DECREASED ( 1 FDA reports)
NIGHT SWEATS ( 1 FDA reports)
OESTROGEN RECEPTOR ASSAY POSITIVE ( 1 FDA reports)
OPPORTUNISTIC INFECTION ( 1 FDA reports)
ORAL INTAKE REDUCED ( 1 FDA reports)
PAIN ( 1 FDA reports)
PAIN IN JAW ( 1 FDA reports)
PCO2 DECREASED ( 1 FDA reports)
PELVIC PAIN ( 1 FDA reports)
PERIPHERAL ARTERIAL OCCLUSIVE DISEASE ( 1 FDA reports)
PLATELET ADHESIVENESS DECREASED ( 1 FDA reports)
PLATELET COUNT INCREASED ( 1 FDA reports)
PNEUMONIA CYTOMEGALOVIRAL ( 1 FDA reports)
PO2 DECREASED ( 1 FDA reports)
PROGESTERONE RECEPTOR ASSAY POSITIVE ( 1 FDA reports)
PROSTATIC SPECIFIC ANTIGEN INCREASED ( 1 FDA reports)
PSOAS ABSCESS ( 1 FDA reports)
PULMONARY THROMBOSIS ( 1 FDA reports)
RADIUS FRACTURE ( 1 FDA reports)
RALES ( 1 FDA reports)
RECURRENT CANCER ( 1 FDA reports)
RED BLOOD CELL COUNT INCREASED ( 1 FDA reports)
REFLUX OESOPHAGITIS ( 1 FDA reports)
RENAL ARTERITIS ( 1 FDA reports)
RENAL FAILURE CHRONIC ( 1 FDA reports)
RESPIRATORY ACIDOSIS ( 1 FDA reports)
RESPIRATORY ARREST ( 1 FDA reports)
RESPIRATORY RATE DECREASED ( 1 FDA reports)
RETINAL DETACHMENT ( 1 FDA reports)
RETRACTED NIPPLE ( 1 FDA reports)
SINUS TACHYCARDIA ( 1 FDA reports)
SPUTUM CULTURE POSITIVE ( 1 FDA reports)
SUDDEN DEATH ( 1 FDA reports)
SUICIDAL IDEATION ( 1 FDA reports)
SURGERY ( 1 FDA reports)
SYNOVECTOMY ( 1 FDA reports)
SYSTEMIC INFLAMMATORY RESPONSE SYNDROME ( 1 FDA reports)
TACHYCARDIA ( 1 FDA reports)
TERMINAL STATE ( 1 FDA reports)
TOXIC SKIN ERUPTION ( 1 FDA reports)
TRANSAMINASES INCREASED ( 1 FDA reports)
TREATMENT NONCOMPLIANCE ( 1 FDA reports)
TREMOR ( 1 FDA reports)
ULNA FRACTURE ( 1 FDA reports)
UNRESPONSIVE TO VERBAL STIMULI ( 1 FDA reports)
UPPER GASTROINTESTINAL HAEMORRHAGE ( 1 FDA reports)
VENOUS THROMBOSIS LIMB ( 1 FDA reports)

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