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

INTERSTITIAL LUNG DISEASE ( 40 FDA reports)
PYREXIA ( 36 FDA reports)
ANAEMIA ( 30 FDA reports)
PLATELET COUNT DECREASED ( 30 FDA reports)
STOMATITIS ( 29 FDA reports)
VOMITING ( 28 FDA reports)
LIVER DISORDER ( 27 FDA reports)
WHITE BLOOD CELL COUNT DECREASED ( 26 FDA reports)
DIARRHOEA ( 24 FDA reports)
RENAL FAILURE ACUTE ( 24 FDA reports)
HEPATIC FUNCTION ABNORMAL ( 23 FDA reports)
NAUSEA ( 22 FDA reports)
CONSTIPATION ( 20 FDA reports)
SEPSIS ( 20 FDA reports)
DISSEMINATED INTRAVASCULAR COAGULATION ( 19 FDA reports)
DRUG ERUPTION ( 19 FDA reports)
PNEUMONIA ( 19 FDA reports)
GASTRIC ULCER ( 18 FDA reports)
CONVULSION ( 17 FDA reports)
PNEUMOCYSTIS JIROVECI PNEUMONIA ( 17 FDA reports)
RESPIRATORY FAILURE ( 16 FDA reports)
DECREASED APPETITE ( 15 FDA reports)
PNEUMONIA ASPIRATION ( 15 FDA reports)
ABDOMINAL PAIN ( 13 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 13 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 13 FDA reports)
HAEMOGLOBIN DECREASED ( 13 FDA reports)
RENAL IMPAIRMENT ( 13 FDA reports)
HYPERTENSION ( 12 FDA reports)
INFECTION ( 12 FDA reports)
RASH ( 12 FDA reports)
ALTERED STATE OF CONSCIOUSNESS ( 11 FDA reports)
C-REACTIVE PROTEIN INCREASED ( 11 FDA reports)
CELLULITIS ( 11 FDA reports)
HISTIOCYTOSIS HAEMATOPHAGIC ( 11 FDA reports)
LEUKOPENIA ( 11 FDA reports)
ASCITES ( 10 FDA reports)
DIZZINESS ( 10 FDA reports)
DYSPNOEA ( 10 FDA reports)
ILEUS ( 10 FDA reports)
LUNG DISORDER ( 10 FDA reports)
MALIGNANT NEOPLASM PROGRESSION ( 10 FDA reports)
BLOOD CREATININE INCREASED ( 9 FDA reports)
GAMMA-GLUTAMYLTRANSFERASE INCREASED ( 9 FDA reports)
GASTRIC ULCER HAEMORRHAGE ( 9 FDA reports)
HYPOKALAEMIA ( 9 FDA reports)
MALAISE ( 9 FDA reports)
MULTI-ORGAN FAILURE ( 9 FDA reports)
MYOCARDIAL INFARCTION ( 9 FDA reports)
RENAL DISORDER ( 9 FDA reports)
BURSITIS ( 8 FDA reports)
CARDIAC FAILURE ( 8 FDA reports)
CARDIAC FAILURE ACUTE ( 8 FDA reports)
ENCEPHALOPATHY ( 8 FDA reports)
FEBRILE NEUTROPENIA ( 8 FDA reports)
HAEMATURIA ( 8 FDA reports)
HEPATIC NEOPLASM MALIGNANT ( 8 FDA reports)
HEPATITIS C ( 8 FDA reports)
NEUTROPHIL COUNT DECREASED ( 8 FDA reports)
PALMAR-PLANTAR ERYTHRODYSAESTHESIA SYNDROME ( 8 FDA reports)
PRINZMETAL ANGINA ( 8 FDA reports)
ABNORMAL BEHAVIOUR ( 7 FDA reports)
BLOOD PRESSURE INCREASED ( 7 FDA reports)
CYTOMEGALOVIRUS INFECTION ( 7 FDA reports)
DUODENAL ULCER ( 7 FDA reports)
GASTRIC CANCER ( 7 FDA reports)
GASTROINTESTINAL HAEMORRHAGE ( 7 FDA reports)
HEPATIC FAILURE ( 7 FDA reports)
OVERDOSE ( 7 FDA reports)
PRURITUS ( 7 FDA reports)
PULMONARY EMBOLISM ( 7 FDA reports)
ABDOMINAL PAIN UPPER ( 6 FDA reports)
ALOPECIA ( 6 FDA reports)
BLOOD PRESSURE DECREASED ( 6 FDA reports)
BLOOD UREA INCREASED ( 6 FDA reports)
BONE MARROW FAILURE ( 6 FDA reports)
DECUBITUS ULCER ( 6 FDA reports)
DELIRIUM ( 6 FDA reports)
GRAFT VERSUS HOST DISEASE ( 6 FDA reports)
HEPATITIS B ( 6 FDA reports)
HYPOGLYCAEMIA ( 6 FDA reports)
MELAENA ( 6 FDA reports)
METASTASES TO LYMPH NODES ( 6 FDA reports)
PHARYNGITIS ( 6 FDA reports)
PNEUMONIA BACTERIAL ( 6 FDA reports)
PULMONARY OEDEMA ( 6 FDA reports)
SEPTIC SHOCK ( 6 FDA reports)
ACUTE RESPIRATORY DISTRESS SYNDROME ( 5 FDA reports)
ARRHYTHMIA ( 5 FDA reports)
BLOOD LACTATE DEHYDROGENASE INCREASED ( 5 FDA reports)
DEATH ( 5 FDA reports)
DEPRESSED LEVEL OF CONSCIOUSNESS ( 5 FDA reports)
DRUG INTERACTION ( 5 FDA reports)
FALL ( 5 FDA reports)
FEELING ABNORMAL ( 5 FDA reports)
HAEMATOCRIT DECREASED ( 5 FDA reports)
HALLUCINATION ( 5 FDA reports)
HEPATIC CIRRHOSIS ( 5 FDA reports)
HYPERTENSIVE ENCEPHALOPATHY ( 5 FDA reports)
JAUNDICE ( 5 FDA reports)
LUNG NEOPLASM MALIGNANT ( 5 FDA reports)
MUCOUS MEMBRANE DISORDER ( 5 FDA reports)
MYCOBACTERIUM KANSASII INFECTION ( 5 FDA reports)
OEDEMA ( 5 FDA reports)
PROTEINURIA ( 5 FDA reports)
PSEUDOMONAS INFECTION ( 5 FDA reports)
RED BLOOD CELL COUNT DECREASED ( 5 FDA reports)
RENAL FAILURE ( 5 FDA reports)
STREPTOCOCCAL INFECTION ( 5 FDA reports)
SWELLING FACE ( 5 FDA reports)
WOUND INFECTION ( 5 FDA reports)
ANAPHYLACTIC SHOCK ( 4 FDA reports)
ATRIAL FIBRILLATION ( 4 FDA reports)
CATHETER RELATED COMPLICATION ( 4 FDA reports)
COMMUNICATION DISORDER ( 4 FDA reports)
CONDITION AGGRAVATED ( 4 FDA reports)
CONGESTIVE CARDIOMYOPATHY ( 4 FDA reports)
CYSTITIS ( 4 FDA reports)
DEEP VEIN THROMBOSIS ( 4 FDA reports)
DERMATITIS ( 4 FDA reports)
EOSINOPHIL COUNT INCREASED ( 4 FDA reports)
GASTROINTESTINAL NECROSIS ( 4 FDA reports)
HYDROCEPHALUS ( 4 FDA reports)
HYPONATRAEMIA ( 4 FDA reports)
ILEAL PERFORATION ( 4 FDA reports)
INFECTIOUS PERITONITIS ( 4 FDA reports)
INTESTINAL ISCHAEMIA ( 4 FDA reports)
INTESTINAL OBSTRUCTION ( 4 FDA reports)
LEG AMPUTATION ( 4 FDA reports)
MUSCULAR WEAKNESS ( 4 FDA reports)
NEUTROPENIA ( 4 FDA reports)
PANCYTOPENIA ( 4 FDA reports)
PROSTATE CANCER ( 4 FDA reports)
PSYCHIATRIC SYMPTOM ( 4 FDA reports)
QUADRIPLEGIA ( 4 FDA reports)
TRANSIENT ISCHAEMIC ATTACK ( 4 FDA reports)
ACUTE GRAFT VERSUS HOST DISEASE ( 3 FDA reports)
ACUTE HEPATIC FAILURE ( 3 FDA reports)
AGRANULOCYTOSIS ( 3 FDA reports)
ANAL ABSCESS ( 3 FDA reports)
ANAPHYLACTIC REACTION ( 3 FDA reports)
ANAPHYLACTOID REACTION ( 3 FDA reports)
ASTHENIA ( 3 FDA reports)
BLOOD ALKALINE PHOSPHATASE INCREASED ( 3 FDA reports)
BONE MARROW DEPRESSION ( 3 FDA reports)
BRADYCARDIA ( 3 FDA reports)
BRAIN OEDEMA ( 3 FDA reports)
BRONCHOPNEUMONIA ( 3 FDA reports)
CEREBRAL HAEMORRHAGE ( 3 FDA reports)
CHOLECYSTITIS ( 3 FDA reports)
COUGH ( 3 FDA reports)
DECREASED ACTIVITY ( 3 FDA reports)
DISORIENTATION ( 3 FDA reports)
DRUG INEFFECTIVE ( 3 FDA reports)
DYSGEUSIA ( 3 FDA reports)
EATING DISORDER ( 3 FDA reports)
ERYTHEMA ( 3 FDA reports)
EYELID DISORDER ( 3 FDA reports)
FATIGUE ( 3 FDA reports)
FUNGAL INFECTION ( 3 FDA reports)
GENERAL PHYSICAL HEALTH DETERIORATION ( 3 FDA reports)
HAEMATEMESIS ( 3 FDA reports)
HAEMORRHAGE SUBCUTANEOUS ( 3 FDA reports)
HEART RATE DECREASED ( 3 FDA reports)
HEPATIC ENZYME INCREASED ( 3 FDA reports)
HEPATIC VEIN OCCLUSION ( 3 FDA reports)
HERPES ZOSTER DISSEMINATED ( 3 FDA reports)
HICCUPS ( 3 FDA reports)
HOT FLUSH ( 3 FDA reports)
HYPERGLYCAEMIA ( 3 FDA reports)
HYPERSENSITIVITY ( 3 FDA reports)
HYPOMAGNESAEMIA ( 3 FDA reports)
HYPOTENSION ( 3 FDA reports)
INFECTIVE SPONDYLITIS ( 3 FDA reports)
LIVER FUNCTION TEST ABNORMAL ( 3 FDA reports)
NEUROPATHY PERIPHERAL ( 3 FDA reports)
OEDEMA PERIPHERAL ( 3 FDA reports)
OESOPHAGEAL CARCINOMA ( 3 FDA reports)
OESOPHAGEAL ULCER ( 3 FDA reports)
OSMOTIC DEMYELINATION SYNDROME ( 3 FDA reports)
OXYGEN SATURATION DECREASED ( 3 FDA reports)
PERICARDITIS ( 3 FDA reports)
PNEUMONIA FUNGAL ( 3 FDA reports)
PSEUDOMONAL SEPSIS ( 3 FDA reports)
PULMONARY MASS ( 3 FDA reports)
RESTLESSNESS ( 3 FDA reports)
RHABDOMYOLYSIS ( 3 FDA reports)
STAPHYLOCOCCAL SEPSIS ( 3 FDA reports)
SUPRAVENTRICULAR TACHYCARDIA ( 3 FDA reports)
THROMBOCYTOPENIA ( 3 FDA reports)
TOXIC EPIDERMAL NECROLYSIS ( 3 FDA reports)
TOXIC SKIN ERUPTION ( 3 FDA reports)
TREMOR ( 3 FDA reports)
TUBERCULOUS PLEURISY ( 3 FDA reports)
URETERIC ANASTOMOSIS COMPLICATION ( 3 FDA reports)
ABULIA ( 2 FDA reports)
ACUTE RESPIRATORY FAILURE ( 2 FDA reports)
AMMONIA INCREASED ( 2 FDA reports)
ANTINUCLEAR ANTIBODY INCREASED ( 2 FDA reports)
ANURIA ( 2 FDA reports)
APHAGIA ( 2 FDA reports)
ARTHRALGIA ( 2 FDA reports)
BACK PAIN ( 2 FDA reports)
BACTERIAL INFECTION ( 2 FDA reports)
BACTERIAL SEPSIS ( 2 FDA reports)
BLINDNESS CORTICAL ( 2 FDA reports)
BLISTER ( 2 FDA reports)
BLOOD BILIRUBIN INCREASED ( 2 FDA reports)
BLOOD CHOLESTEROL DECREASED ( 2 FDA reports)
BLOOD CREATININE DECREASED ( 2 FDA reports)
BLOOD GLUCOSE INCREASED ( 2 FDA reports)
BLOOD PH DECREASED ( 2 FDA reports)
BLOOD URIC ACID INCREASED ( 2 FDA reports)
BRONCHITIS ( 2 FDA reports)
CANDIDIASIS ( 2 FDA reports)
CARDIAC ARREST ( 2 FDA reports)
CENTRAL PONTINE MYELINOLYSIS ( 2 FDA reports)
CEREBRAL INFARCTION ( 2 FDA reports)
CHEILITIS ( 2 FDA reports)
CROSSMATCH INCOMPATIBLE ( 2 FDA reports)
CRYPTOGENIC ORGANISING PNEUMONIA ( 2 FDA reports)
CYTOMEGALOVIRUS COLITIS ( 2 FDA reports)
DEHYDRATION ( 2 FDA reports)
DEMYELINATION ( 2 FDA reports)
DERMATITIS ALLERGIC ( 2 FDA reports)
DERMATITIS EXFOLIATIVE ( 2 FDA reports)
DEVICE INTERACTION ( 2 FDA reports)
DISEASE PROGRESSION ( 2 FDA reports)
DIVERTICULITIS ( 2 FDA reports)
DRUG LEVEL INCREASED ( 2 FDA reports)
DRUG-INDUCED LIVER INJURY ( 2 FDA reports)
DYSARTHRIA ( 2 FDA reports)
DYSLALIA ( 2 FDA reports)
DYSURIA ( 2 FDA reports)
ENCEPHALITIS ( 2 FDA reports)
ENDOCARDITIS NONINFECTIVE ( 2 FDA reports)
ENTERITIS INFECTIOUS ( 2 FDA reports)
EPILEPSY ( 2 FDA reports)
EYE LUXATION ( 2 FDA reports)
FAECES DISCOLOURED ( 2 FDA reports)
FLUSHING ( 2 FDA reports)
GASTRIC CANCER STAGE III ( 2 FDA reports)
GASTRITIS ( 2 FDA reports)
GASTROENTERITIS ( 2 FDA reports)
GENERALISED ERYTHEMA ( 2 FDA reports)
GRAFT VERSUS HOST DISEASE IN LUNG ( 2 FDA reports)
GRAND MAL CONVULSION ( 2 FDA reports)
GRANULOCYTOPENIA ( 2 FDA reports)
HAEMODIALYSIS ( 2 FDA reports)
HEPATIC INFARCTION ( 2 FDA reports)
HEPATIC NEOPLASM MALIGNANT NON-RESECTABLE ( 2 FDA reports)
HEPATITIS ( 2 FDA reports)
HYPERAMMONAEMIA ( 2 FDA reports)
HYPERCHLORAEMIA ( 2 FDA reports)
HYPERCOAGULATION ( 2 FDA reports)
HYPERHIDROSIS ( 2 FDA reports)
HYPERKALAEMIA ( 2 FDA reports)
HYPERNATRAEMIA ( 2 FDA reports)
HYPERURICAEMIA ( 2 FDA reports)
ILEUS PARALYTIC ( 2 FDA reports)
INFUSION RELATED REACTION ( 2 FDA reports)
INJECTION SITE EXTRAVASATION ( 2 FDA reports)
KAPOSI'S SARCOMA ( 2 FDA reports)
LIVER CARCINOMA RUPTURED ( 2 FDA reports)
LYMPHOCYTE COUNT INCREASED ( 2 FDA reports)
METASTASES TO ABDOMINAL CAVITY ( 2 FDA reports)
MUSCLE SPASMS ( 2 FDA reports)
MYOCLONUS ( 2 FDA reports)
MYOSITIS ( 2 FDA reports)
NEOPLASM MALIGNANT ( 2 FDA reports)
OESOPHAGEAL STENOSIS ( 2 FDA reports)
OESOPHAGEAL ULCER PERFORATION ( 2 FDA reports)
OESOPHAGEAL VARICES HAEMORRHAGE ( 2 FDA reports)
PAIN IN EXTREMITY ( 2 FDA reports)
PALPITATIONS ( 2 FDA reports)
PANCREATITIS ACUTE ( 2 FDA reports)
PERIOSTITIS ( 2 FDA reports)
PNEUMOTHORAX ( 2 FDA reports)
POLYOMAVIRUS TEST POSITIVE ( 2 FDA reports)
PROTEIN TOTAL DECREASED ( 2 FDA reports)
PROTEIN-LOSING GASTROENTEROPATHY ( 2 FDA reports)
PULMONARY ALVEOLAR HAEMORRHAGE ( 2 FDA reports)
RASH ERYTHEMATOUS ( 2 FDA reports)
RASH MACULO-PAPULAR ( 2 FDA reports)
RECTAL PERFORATION ( 2 FDA reports)
RENAL CELL CARCINOMA ( 2 FDA reports)
RESPIRATORY ARREST ( 2 FDA reports)
RETROPERITONEAL ABSCESS ( 2 FDA reports)
REVERSIBLE POSTERIOR LEUKOENCEPHALOPATHY SYNDROME ( 2 FDA reports)
SINUSITIS ( 2 FDA reports)
SKIN EXFOLIATION ( 2 FDA reports)
SOMNOLENCE ( 2 FDA reports)
SPLEEN DISORDER ( 2 FDA reports)
STAPHYLOCOCCAL INFECTION ( 2 FDA reports)
STRIDOR ( 2 FDA reports)
SWELLING ( 2 FDA reports)
THROMBOPHLEBITIS MIGRANS ( 2 FDA reports)
URINARY INCONTINENCE ( 2 FDA reports)
URINARY RETENTION ( 2 FDA reports)
URINE OUTPUT DECREASED ( 2 FDA reports)
VARICELLA ( 2 FDA reports)
VISION BLURRED ( 2 FDA reports)
VISUAL IMPAIRMENT ( 2 FDA reports)
WHITE BLOOD CELL COUNT INCREASED ( 2 FDA reports)
ABASIA ( 1 FDA reports)
ABDOMINAL DISCOMFORT ( 1 FDA reports)
ADRENAL INSUFFICIENCY ( 1 FDA reports)
ADVERSE REACTION ( 1 FDA reports)
ALCOHOL USE ( 1 FDA reports)
ANGINA PECTORIS ( 1 FDA reports)
ANOREXIA ( 1 FDA reports)
AORTIC ANEURYSM RUPTURE ( 1 FDA reports)
APALLIC SYNDROME ( 1 FDA reports)
APHASIA ( 1 FDA reports)
APPENDICITIS ( 1 FDA reports)
ARTHRITIS ( 1 FDA reports)
ARTHRITIS BACTERIAL ( 1 FDA reports)
ATRIOVENTRICULAR BLOCK ( 1 FDA reports)
B-CELL LYMPHOMA ( 1 FDA reports)
BLOOD ALBUMIN DECREASED ( 1 FDA reports)
BLOOD AMYLASE INCREASED ( 1 FDA reports)
BLOOD BILIRUBIN DECREASED ( 1 FDA reports)
BLOOD CHOLESTEROL INCREASED ( 1 FDA reports)
BLOOD POTASSIUM INCREASED ( 1 FDA reports)
BLOOD SODIUM DECREASED ( 1 FDA reports)
BLOOD TRIGLYCERIDES INCREASED ( 1 FDA reports)
BRAIN NATRIURETIC PEPTIDE INCREASED ( 1 FDA reports)
CACHEXIA ( 1 FDA reports)
CANDIDA SEROLOGY POSITIVE ( 1 FDA reports)
CARDIAC FAILURE CHRONIC ( 1 FDA reports)
CARDIO-RESPIRATORY ARREST ( 1 FDA reports)
CATARACT ( 1 FDA reports)
CENTRAL-ALVEOLAR HYPOVENTILATION ( 1 FDA reports)
CEREBRAL ISCHAEMIA ( 1 FDA reports)
CHEST DISCOMFORT ( 1 FDA reports)
CHEST PAIN ( 1 FDA reports)
CHEST X-RAY ABNORMAL ( 1 FDA reports)
CHEYNE-STOKES RESPIRATION ( 1 FDA reports)
CHOLANGITIS ( 1 FDA reports)
CHOLANGITIS ACUTE ( 1 FDA reports)
CHOLESTATIC LIVER INJURY ( 1 FDA reports)
COLORECTAL CANCER ( 1 FDA reports)
COMPLICATIONS OF TRANSPLANTED KIDNEY ( 1 FDA reports)
CONVERSION DISORDER ( 1 FDA reports)
COORDINATION ABNORMAL ( 1 FDA reports)
CROHN'S DISEASE ( 1 FDA reports)
CRYPTOGENIC ORGANIZING PNEUMONIA ( 1 FDA reports)
CULTURE POSITIVE ( 1 FDA reports)
CYTOMEGALOVIRUS ENTEROCOLITIS ( 1 FDA reports)
CYTOMEGALOVIRUS VIRAEMIA ( 1 FDA reports)
DELAYED RECOVERY FROM ANAESTHESIA ( 1 FDA reports)
DELUSION ( 1 FDA reports)
DELUSIONAL DISORDER, UNSPECIFIED TYPE ( 1 FDA reports)
DENTAL CARIES ( 1 FDA reports)
DERMATITIS ACNEIFORM ( 1 FDA reports)
DIABETES MELLITUS ( 1 FDA reports)
DIALYSIS ( 1 FDA reports)
DIFFICULTY IN WALKING ( 1 FDA reports)
DROWNING ( 1 FDA reports)
DRUG SPECIFIC ANTIBODY PRESENT ( 1 FDA reports)
DRY MOUTH ( 1 FDA reports)
DYSPHAGIA ( 1 FDA reports)
DYSPHONIA ( 1 FDA reports)
DYSSTASIA ( 1 FDA reports)
EJECTION FRACTION DECREASED ( 1 FDA reports)
ELECTROCARDIOGRAM ST SEGMENT DEPRESSION ( 1 FDA reports)
ELECTROENCEPHALOGRAM ABNORMAL ( 1 FDA reports)
ENTEROCOCCAL INFECTION ( 1 FDA reports)
ENTEROCOLITIS HAEMORRHAGIC ( 1 FDA reports)
ERYTHEMA MULTIFORME ( 1 FDA reports)
FEELING HOT ( 1 FDA reports)
FOOD CRAVING ( 1 FDA reports)
GAIT DISTURBANCE ( 1 FDA reports)
GANGRENE ( 1 FDA reports)
GASTRIC MUCOSAL LESION ( 1 FDA reports)
GASTROENTERITIS STAPHYLOCOCCAL ( 1 FDA reports)
GASTROINTESTINAL DISORDER ( 1 FDA reports)
GLOSSODYNIA ( 1 FDA reports)
GOUT ( 1 FDA reports)
GRANULOCYTE COUNT DECREASED ( 1 FDA reports)
HAEMOPTYSIS ( 1 FDA reports)
HAEMORRHAGE ( 1 FDA reports)
HAEMORRHAGE INTRACRANIAL ( 1 FDA reports)
HEART RATE INCREASED ( 1 FDA reports)
HELICOBACTER INFECTION ( 1 FDA reports)
HEPATIC ENCEPHALOPATHY ( 1 FDA reports)
HEPATIC NECROSIS ( 1 FDA reports)
HYPERCAPNIA ( 1 FDA reports)
HYPERKINESIA ( 1 FDA reports)
HYPOPHAGIA ( 1 FDA reports)
HYPOPHOSPHATAEMIA ( 1 FDA reports)
HYPOXIA ( 1 FDA reports)
HYPOXIC-ISCHAEMIC ENCEPHALOPATHY ( 1 FDA reports)
IMMUNOSUPPRESSION ( 1 FDA reports)
INFECTED EPIDERMAL CYST ( 1 FDA reports)
INFECTED SKIN ULCER ( 1 FDA reports)
INGROWING NAIL ( 1 FDA reports)
INSOMNIA ( 1 FDA reports)
JAUNDICE CHOLESTATIC ( 1 FDA reports)
LARYNGEAL OEDEMA ( 1 FDA reports)
LIPASE INCREASED ( 1 FDA reports)
LIVER TRANSPLANT ( 1 FDA reports)
LOGORRHOEA ( 1 FDA reports)
LUNG INFILTRATION ( 1 FDA reports)
LYMPHOCYTE STIMULATION TEST POSITIVE ( 1 FDA reports)
MEMORY IMPAIRMENT ( 1 FDA reports)
METABOLIC ACIDOSIS ( 1 FDA reports)
METASTASES TO BONE ( 1 FDA reports)
METASTASIS ( 1 FDA reports)
MUSCULOSKELETAL CHEST PAIN ( 1 FDA reports)
MYALGIA ( 1 FDA reports)
NAIL DISORDER ( 1 FDA reports)
NASOPHARYNGITIS ( 1 FDA reports)
NECK PAIN ( 1 FDA reports)
NEPHROGENIC ANAEMIA ( 1 FDA reports)
NEURECTOMY ( 1 FDA reports)
NO THERAPEUTIC RESPONSE ( 1 FDA reports)
NON-SMALL CELL LUNG CANCER ( 1 FDA reports)
OROPHARYNGEAL PAIN ( 1 FDA reports)
OSTEOARTHRITIS ( 1 FDA reports)
OSTEOPOROSIS ( 1 FDA reports)
OVARIAN CANCER ( 1 FDA reports)
OVARIAN CANCER RECURRENT ( 1 FDA reports)
PALLOR ( 1 FDA reports)
PARONYCHIA ( 1 FDA reports)
PATHOGEN RESISTANCE ( 1 FDA reports)
PERIPHERAL COLDNESS ( 1 FDA reports)
PHARYNGEAL OEDEMA ( 1 FDA reports)
PLEURAL EFFUSION ( 1 FDA reports)
PNEUMONITIS ( 1 FDA reports)
PSEUDOMEMBRANOUS COLITIS ( 1 FDA reports)
PSYCHOTIC DISORDER ( 1 FDA reports)
PULMONARY TUBERCULOSIS ( 1 FDA reports)
PURPURA ( 1 FDA reports)
RADIATION OESOPHAGITIS ( 1 FDA reports)
RADIATION PNEUMONITIS ( 1 FDA reports)
REFUSAL OF TREATMENT BY PATIENT ( 1 FDA reports)
RIB FRACTURE ( 1 FDA reports)
SENSATION OF FOREIGN BODY ( 1 FDA reports)
SHOCK HAEMORRHAGIC ( 1 FDA reports)
SKIN ULCER ( 1 FDA reports)
SPEECH DISORDER ( 1 FDA reports)
SPINAL COMPRESSION FRACTURE ( 1 FDA reports)
STENOTROPHOMONAS INFECTION ( 1 FDA reports)
SUDDEN DEATH ( 1 FDA reports)
SUICIDAL IDEATION ( 1 FDA reports)
SYSTEMIC INFLAMMATORY RESPONSE SYNDROME ( 1 FDA reports)
THERMAL BURN ( 1 FDA reports)
THROMBOSIS ( 1 FDA reports)
TINEA INFECTION ( 1 FDA reports)
TREATMENT NONCOMPLIANCE ( 1 FDA reports)
TUBERCULOSIS ( 1 FDA reports)
TUMOUR HAEMORRHAGE ( 1 FDA reports)
UPPER GASTROINTESTINAL HAEMORRHAGE ( 1 FDA reports)
UPPER RESPIRATORY TRACT INFLAMMATION ( 1 FDA reports)
VERTIGO ( 1 FDA reports)
WEIGHT DECREASED ( 1 FDA reports)
WHEEZING ( 1 FDA reports)

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