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

NAUSEA ( 58 FDA reports)
FEBRILE NEUTROPENIA ( 54 FDA reports)
VOMITING ( 39 FDA reports)
DIARRHOEA ( 38 FDA reports)
ASTHENIA ( 33 FDA reports)
DECREASED APPETITE ( 27 FDA reports)
MUCOSAL INFLAMMATION ( 24 FDA reports)
PAIN ( 23 FDA reports)
ALOPECIA ( 21 FDA reports)
ABDOMINAL PAIN ( 20 FDA reports)
FATIGUE ( 20 FDA reports)
NEUTROPENIA ( 19 FDA reports)
BLOOD DISORDER ( 18 FDA reports)
ANAEMIA ( 17 FDA reports)
DIZZINESS ( 17 FDA reports)
PYREXIA ( 16 FDA reports)
CHOLECYSTITIS CHRONIC ( 15 FDA reports)
CONSTIPATION ( 15 FDA reports)
DYSPNOEA ( 15 FDA reports)
BACTERAEMIA ( 14 FDA reports)
CHOLELITHIASIS ( 13 FDA reports)
DEATH ( 13 FDA reports)
INFECTION ( 13 FDA reports)
HYPOTENSION ( 12 FDA reports)
EPISTAXIS ( 11 FDA reports)
GALLBLADDER DISORDER ( 11 FDA reports)
ABDOMINAL PAIN UPPER ( 10 FDA reports)
CARDIOTOXICITY ( 9 FDA reports)
PNEUMONIA ( 9 FDA reports)
RENAL FAILURE ( 9 FDA reports)
RESPIRATORY FAILURE ( 9 FDA reports)
THROMBOCYTOPENIA ( 9 FDA reports)
ARTHRALGIA ( 8 FDA reports)
DEHYDRATION ( 8 FDA reports)
INTERSTITIAL LUNG DISEASE ( 8 FDA reports)
MALAISE ( 8 FDA reports)
NEUROPATHY PERIPHERAL ( 8 FDA reports)
PANCREATITIS ( 8 FDA reports)
CHOLECYSTITIS ( 7 FDA reports)
DRUG INEFFECTIVE ( 7 FDA reports)
DYSPHAGIA ( 7 FDA reports)
GENERAL PHYSICAL HEALTH DETERIORATION ( 7 FDA reports)
HAEMOGLOBIN DECREASED ( 7 FDA reports)
HEADACHE ( 7 FDA reports)
LEUKOPENIA ( 7 FDA reports)
PANCYTOPENIA ( 7 FDA reports)
PLATELET COUNT DECREASED ( 7 FDA reports)
SEPSIS ( 7 FDA reports)
ABASIA ( 6 FDA reports)
CARDIAC ARREST ( 6 FDA reports)
CELLULITIS ( 6 FDA reports)
CEREBROVASCULAR ACCIDENT ( 6 FDA reports)
COMPRESSION FRACTURE ( 6 FDA reports)
CONVULSION ( 6 FDA reports)
DISEASE PROGRESSION ( 6 FDA reports)
ERYTHEMA ( 6 FDA reports)
MALIGNANT NEOPLASM PROGRESSION ( 6 FDA reports)
WEIGHT DECREASED ( 6 FDA reports)
ANOREXIA ( 5 FDA reports)
BILIARY DYSKINESIA ( 5 FDA reports)
BLOOD CREATININE INCREASED ( 5 FDA reports)
BLOOD PRESSURE INCREASED ( 5 FDA reports)
CHILLS ( 5 FDA reports)
COLITIS ( 5 FDA reports)
DRUG TOXICITY ( 5 FDA reports)
DYSPEPSIA ( 5 FDA reports)
FALL ( 5 FDA reports)
GASTROINTESTINAL NECROSIS ( 5 FDA reports)
HAEMORRHAGE ( 5 FDA reports)
INFLUENZA LIKE ILLNESS ( 5 FDA reports)
LOSS OF CONSCIOUSNESS ( 5 FDA reports)
MUSCULAR WEAKNESS ( 5 FDA reports)
PAIN IN EXTREMITY ( 5 FDA reports)
PHOTOPHOBIA ( 5 FDA reports)
SLOW RESPONSE TO STIMULI ( 5 FDA reports)
SOMNOLENCE ( 5 FDA reports)
TOXICITY TO VARIOUS AGENTS ( 5 FDA reports)
URINARY INCONTINENCE ( 5 FDA reports)
AGGRESSION ( 4 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 4 FDA reports)
BLOOD GLUCOSE INCREASED ( 4 FDA reports)
BREAKTHROUGH PAIN ( 4 FDA reports)
CHEST PAIN ( 4 FDA reports)
CONFUSIONAL STATE ( 4 FDA reports)
COUGH ( 4 FDA reports)
DEPRESSION ( 4 FDA reports)
DRUG DIVERSION ( 4 FDA reports)
DRUG EXPOSURE DURING PREGNANCY ( 4 FDA reports)
FLANK PAIN ( 4 FDA reports)
GALLBLADDER INJURY ( 4 FDA reports)
GASTROINTESTINAL DISORDER ( 4 FDA reports)
GASTROOESOPHAGEAL REFLUX DISEASE ( 4 FDA reports)
HEART RATE DECREASED ( 4 FDA reports)
HYPERTENSION ( 4 FDA reports)
HYPOPHAGIA ( 4 FDA reports)
INJECTION SITE PAIN ( 4 FDA reports)
INSOMNIA ( 4 FDA reports)
LETHARGY ( 4 FDA reports)
LIVER FUNCTION TEST ABNORMAL ( 4 FDA reports)
LOWER RESPIRATORY TRACT INFECTION ( 4 FDA reports)
MEMORY IMPAIRMENT ( 4 FDA reports)
MULTI-ORGAN FAILURE ( 4 FDA reports)
MYOCARDIAL INFARCTION ( 4 FDA reports)
OEDEMA ( 4 FDA reports)
PROCEDURAL PAIN ( 4 FDA reports)
PSYCHOTIC DISORDER ( 4 FDA reports)
TACHYCARDIA ( 4 FDA reports)
VISION BLURRED ( 4 FDA reports)
ABDOMINAL DISCOMFORT ( 3 FDA reports)
ABNORMAL CLOTTING FACTOR ( 3 FDA reports)
ABORTION SPONTANEOUS ( 3 FDA reports)
ACUTE FEBRILE NEUTROPHILIC DERMATOSIS ( 3 FDA reports)
AMNESIA ( 3 FDA reports)
ANGINA PECTORIS ( 3 FDA reports)
ANXIETY ( 3 FDA reports)
BLOOD PRESSURE DECREASED ( 3 FDA reports)
CAECITIS ( 3 FDA reports)
CHOLECYSTECTOMY ( 3 FDA reports)
CONDITION AGGRAVATED ( 3 FDA reports)
CRYPTOGENIC ORGANIZING PNEUMONIA ( 3 FDA reports)
DEMENTIA ( 3 FDA reports)
DEVICE RELATED INFECTION ( 3 FDA reports)
DRUG ERUPTION ( 3 FDA reports)
DRUG INTERACTION ( 3 FDA reports)
DYSGEUSIA ( 3 FDA reports)
EMOTIONAL DISTRESS ( 3 FDA reports)
FLUID INTAKE RESTRICTION ( 3 FDA reports)
FUNGAL INFECTION ( 3 FDA reports)
GAMMA-GLUTAMYLTRANSFERASE INCREASED ( 3 FDA reports)
HAEMATOCRIT ( 3 FDA reports)
HAEMOGLOBIN ( 3 FDA reports)
HYPERSENSITIVITY ( 3 FDA reports)
HYPONATRAEMIA ( 3 FDA reports)
INJURY ( 3 FDA reports)
JOINT SWELLING ( 3 FDA reports)
LIPASE INCREASED ( 3 FDA reports)
LYMPHOCYTE COUNT ( 3 FDA reports)
MENTAL STATUS CHANGES ( 3 FDA reports)
METABOLIC ACIDOSIS ( 3 FDA reports)
MIGRAINE ( 3 FDA reports)
MOBILITY DECREASED ( 3 FDA reports)
MUSCLE SPASMS ( 3 FDA reports)
MYOCARDIAL ISCHAEMIA ( 3 FDA reports)
MYOSITIS ( 3 FDA reports)
NEUTROPENIC SEPSIS ( 3 FDA reports)
OEDEMA PERIPHERAL ( 3 FDA reports)
PALMAR-PLANTAR ERYTHRODYSAESTHESIA SYNDROME ( 3 FDA reports)
PHARYNGOLARYNGEAL PAIN ( 3 FDA reports)
PLEURAL EFFUSION ( 3 FDA reports)
PRESYNCOPE ( 3 FDA reports)
PRODUCTIVE COUGH ( 3 FDA reports)
PROTEIN TOTAL INCREASED ( 3 FDA reports)
PULMONARY EMBOLISM ( 3 FDA reports)
RED BLOOD CELL COUNT ( 3 FDA reports)
SCAR ( 3 FDA reports)
SINUSITIS ( 3 FDA reports)
STAPHYLOCOCCAL INFECTION ( 3 FDA reports)
URINARY TRACT INFECTION ( 3 FDA reports)
URTICARIA ( 3 FDA reports)
WHITE BLOOD CELL COUNT ( 3 FDA reports)
ABDOMINAL INFECTION ( 2 FDA reports)
ABSCESS ( 2 FDA reports)
ACNE ( 2 FDA reports)
ACUTE RESPIRATORY DISTRESS SYNDROME ( 2 FDA reports)
ARRHYTHMIA ( 2 FDA reports)
ARTHRITIS ( 2 FDA reports)
ASCITES ( 2 FDA reports)
ATRIAL FIBRILLATION ( 2 FDA reports)
BACK PAIN ( 2 FDA reports)
BLINDNESS ( 2 FDA reports)
BLISTER ( 2 FDA reports)
BLOOD ALBUMIN ABNORMAL ( 2 FDA reports)
BLOOD CREATINE PHOSPHOKINASE INCREASED ( 2 FDA reports)
BLOOD GLUCOSE DECREASED ( 2 FDA reports)
BODY TEMPERATURE INCREASED ( 2 FDA reports)
BONE PAIN ( 2 FDA reports)
BRONCHITIS ( 2 FDA reports)
BRONCHOPULMONARY ASPERGILLOSIS ( 2 FDA reports)
BUTTOCK PAIN ( 2 FDA reports)
CARDIAC FAILURE CONGESTIVE ( 2 FDA reports)
CENTRAL NERVOUS SYSTEM LYMPHOMA ( 2 FDA reports)
CHOLECYSTITIS ACUTE ( 2 FDA reports)
CHRONIC OBSTRUCTIVE PULMONARY DISEASE ( 2 FDA reports)
CLOSTRIDIUM DIFFICILE SEPSIS ( 2 FDA reports)
COLD SWEAT ( 2 FDA reports)
COMA ( 2 FDA reports)
CONTUSION ( 2 FDA reports)
CORONARY ARTERY DISEASE ( 2 FDA reports)
CYCLIC VOMITING SYNDROME ( 2 FDA reports)
DERMATITIS ( 2 FDA reports)
DIARRHOEA HAEMORRHAGIC ( 2 FDA reports)
DIFFICULTY IN WALKING ( 2 FDA reports)
DRUG HYPERSENSITIVITY ( 2 FDA reports)
DYSARTHRIA ( 2 FDA reports)
EATING DISORDER ( 2 FDA reports)
ELECTROLYTE IMBALANCE ( 2 FDA reports)
EYE INFLAMMATION ( 2 FDA reports)
FEAR ( 2 FDA reports)
FEELING ABNORMAL ( 2 FDA reports)
FLUID RETENTION ( 2 FDA reports)
GALLBLADDER CHOLESTEROLOSIS ( 2 FDA reports)
GANGRENE ( 2 FDA reports)
GASTRITIS ( 2 FDA reports)
GRAND MAL CONVULSION ( 2 FDA reports)
HEART RATE INCREASED ( 2 FDA reports)
HEPATIC ENZYME INCREASED ( 2 FDA reports)
HEPATITIS TOXIC ( 2 FDA reports)
HIATUS HERNIA ( 2 FDA reports)
HOSPITALISATION ( 2 FDA reports)
HYPERAESTHESIA ( 2 FDA reports)
HYPERKALAEMIA ( 2 FDA reports)
HYPOKALAEMIA ( 2 FDA reports)
IMMUNODEFICIENCY ( 2 FDA reports)
INFLAMMATION ( 2 FDA reports)
INJECTION SITE IRRITATION ( 2 FDA reports)
JOINT WARMTH ( 2 FDA reports)
LABORATORY TEST ABNORMAL ( 2 FDA reports)
LACTIC ACIDOSIS ( 2 FDA reports)
LIP ULCERATION ( 2 FDA reports)
LOSS OF CONTROL OF LEGS ( 2 FDA reports)
LUNG DISORDER ( 2 FDA reports)
LYMPHADENOPATHY ( 2 FDA reports)
MEAN CELL HAEMOGLOBIN ( 2 FDA reports)
MEAN CELL HAEMOGLOBIN CONCENTRATION ( 2 FDA reports)
MULTIPLE SCLEROSIS ( 2 FDA reports)
MUSCLE SPASTICITY ( 2 FDA reports)
MUSCULOSKELETAL PAIN ( 2 FDA reports)
MYALGIA ( 2 FDA reports)
NEPHROPATHY TOXIC ( 2 FDA reports)
ORAL PAIN ( 2 FDA reports)
ORAL SOFT TISSUE DISORDER ( 2 FDA reports)
PAIN OF SKIN ( 2 FDA reports)
PAINFUL RESPIRATION ( 2 FDA reports)
PANIC ATTACK ( 2 FDA reports)
PARAINFLUENZAE VIRUS INFECTION ( 2 FDA reports)
PARAMETRITIS ( 2 FDA reports)
PERICARDIAL EFFUSION ( 2 FDA reports)
PERICARDITIS ( 2 FDA reports)
PLACENTA PRAEVIA ( 2 FDA reports)
PLEURITIC PAIN ( 2 FDA reports)
PNEUMONIA ASPIRATION ( 2 FDA reports)
PNEUMONITIS ( 2 FDA reports)
PREGNANCY ( 2 FDA reports)
PREMATURE BABY ( 2 FDA reports)
PREMATURE LABOUR ( 2 FDA reports)
PRODUCT QUALITY ISSUE ( 2 FDA reports)
PYODERMA GANGRENOSUM ( 2 FDA reports)
RASH ( 2 FDA reports)
RASH PAPULAR ( 2 FDA reports)
RED BLOOD CELL COUNT DECREASED ( 2 FDA reports)
RENAL IMPAIRMENT ( 2 FDA reports)
ROAD TRAFFIC ACCIDENT ( 2 FDA reports)
SCLEROSING ENCAPSULATING PERITONITIS ( 2 FDA reports)
SERRATIA INFECTION ( 2 FDA reports)
SHOCK ( 2 FDA reports)
SINUS TACHYCARDIA ( 2 FDA reports)
SKIN EXFOLIATION ( 2 FDA reports)
SKIN FISSURES ( 2 FDA reports)
SKIN LESION ( 2 FDA reports)
SPEECH DISORDER ( 2 FDA reports)
STOMATITIS ( 2 FDA reports)
STRABISMUS ( 2 FDA reports)
STRIDOR ( 2 FDA reports)
SUDDEN DEATH ( 2 FDA reports)
SWELLING ( 2 FDA reports)
TENDERNESS ( 2 FDA reports)
THROMBOSIS ( 2 FDA reports)
TINNITUS ( 2 FDA reports)
TONSILLAR DISORDER ( 2 FDA reports)
TREMOR ( 2 FDA reports)
TRISMUS ( 2 FDA reports)
UNEVALUABLE EVENT ( 2 FDA reports)
UTERINE LEIOMYOMA ( 2 FDA reports)
VAGINAL HAEMORRHAGE ( 2 FDA reports)
WHITE BLOOD CELL COUNT DECREASED ( 2 FDA reports)
ABDOMINAL ADHESIONS ( 1 FDA reports)
ABDOMINAL DISTENSION ( 1 FDA reports)
ABDOMINAL PAIN LOWER ( 1 FDA reports)
ACNE CYSTIC ( 1 FDA reports)
ACUTE PULMONARY OEDEMA ( 1 FDA reports)
ACUTE RESPIRATORY FAILURE ( 1 FDA reports)
ADVERSE DRUG REACTION ( 1 FDA reports)
ADVERSE EVENT ( 1 FDA reports)
AGITATION ( 1 FDA reports)
ALDOLASE INCREASED ( 1 FDA reports)
AMNIORRHOEA ( 1 FDA reports)
AMNIOTIC FLUID VOLUME INCREASED ( 1 FDA reports)
ANAPHYLACTIC SHOCK ( 1 FDA reports)
ANHEDONIA ( 1 FDA reports)
ANTICONVULSANT DRUG LEVEL ABNORMAL ( 1 FDA reports)
ANTICONVULSANT DRUG LEVEL ABOVE THERAPEUTIC ( 1 FDA reports)
ANTICONVULSANT DRUG LEVEL BELOW THERAPEUTIC ( 1 FDA reports)
ANURIA ( 1 FDA reports)
APHASIA ( 1 FDA reports)
APNOEIC ATTACK ( 1 FDA reports)
APRAXIA ( 1 FDA reports)
ARACHNOIDITIS ( 1 FDA reports)
ARTERY DISSECTION ( 1 FDA reports)
ASPARTATE AMINOTRANSFERASE ( 1 FDA reports)
ATRIAL FLUTTER ( 1 FDA reports)
ATRIOVENTRICULAR BLOCK ( 1 FDA reports)
AUTONOMIC NEUROPATHY ( 1 FDA reports)
BACTERIAL INFECTION ( 1 FDA reports)
BLADDER DISORDER ( 1 FDA reports)
BLOOD CALCIUM DECREASED ( 1 FDA reports)
BLOOD CREATINE INCREASED ( 1 FDA reports)
BLOOD CULTURE POSITIVE ( 1 FDA reports)
BLOOD IRON DECREASED ( 1 FDA reports)
BLOOD PRESSURE FLUCTUATION ( 1 FDA reports)
BLOOD SODIUM DECREASED ( 1 FDA reports)
BLOOD TEST ABNORMAL ( 1 FDA reports)
BLOOD UREA INCREASED ( 1 FDA reports)
BODY TEMPERATURE DECREASED ( 1 FDA reports)
BONE CYST ( 1 FDA reports)
BONE GRAFT ( 1 FDA reports)
BONE MARROW TOXICITY ( 1 FDA reports)
BREAST PAIN ( 1 FDA reports)
BRONCHOPNEUMONIA ( 1 FDA reports)
BUNDLE BRANCH BLOCK ( 1 FDA reports)
CANDIDIASIS ( 1 FDA reports)
CAPILLARY LEAK SYNDROME ( 1 FDA reports)
CARDIAC DISORDER ( 1 FDA reports)
CARDIAC FAILURE ( 1 FDA reports)
CARDIAC FIBRILLATION ( 1 FDA reports)
CARDIAC MURMUR ( 1 FDA reports)
CARDIO-RESPIRATORY ARREST ( 1 FDA reports)
CARDIO-RESPIRATORY ARREST NEONATAL ( 1 FDA reports)
CEREBRAL ARTERY THROMBOSIS ( 1 FDA reports)
CEREBRAL HAEMORRHAGE ( 1 FDA reports)
CEREBRAL INFARCTION ( 1 FDA reports)
CHEST DISCOMFORT ( 1 FDA reports)
CHEST X-RAY ABNORMAL ( 1 FDA reports)
CHRONIC LYMPHOCYTIC LEUKAEMIA ( 1 FDA reports)
COAGULATION TIME PROLONGED ( 1 FDA reports)
COLITIS ISCHAEMIC ( 1 FDA reports)
COLONIC POLYP ( 1 FDA reports)
COLONIC PSEUDO-OBSTRUCTION ( 1 FDA reports)
CONCUSSION ( 1 FDA reports)
CONVERSION DISORDER ( 1 FDA reports)
COORDINATION ABNORMAL ( 1 FDA reports)
CRUSH INJURY ( 1 FDA reports)
CRYPTOGENIC ORGANISING PNEUMONIA ( 1 FDA reports)
CYSTITIS ( 1 FDA reports)
CYTOKINE RELEASE SYNDROME ( 1 FDA reports)
DECREASED ACTIVITY ( 1 FDA reports)
DEEP VEIN THROMBOSIS ( 1 FDA reports)
DENTAL CARIES ( 1 FDA reports)
DISORIENTATION ( 1 FDA reports)
DIZZINESS POSTURAL ( 1 FDA reports)
DRUG INTOLERANCE ( 1 FDA reports)
DRY GANGRENE ( 1 FDA reports)
DYSKINESIA ( 1 FDA reports)
DYSPHONIA ( 1 FDA reports)
DYSTONIA ( 1 FDA reports)
EAR HAEMORRHAGE ( 1 FDA reports)
ELECTROCARDIOGRAM ABNORMAL ( 1 FDA reports)
ELECTROCARDIOGRAM QT PROLONGED ( 1 FDA reports)
EMPHYSEMA ( 1 FDA reports)
EXTREMITY NECROSIS ( 1 FDA reports)
EYE PAIN ( 1 FDA reports)
FAILURE TO THRIVE ( 1 FDA reports)
FOETAL HEART RATE DISORDER ( 1 FDA reports)
FOETAL HYPOKINESIA ( 1 FDA reports)
GAIT DISTURBANCE ( 1 FDA reports)
GALLBLADDER OPERATION ( 1 FDA reports)
GASTRIC CANCER ( 1 FDA reports)
GASTRIC CANCER STAGE IV ( 1 FDA reports)
GASTRIC DISORDER ( 1 FDA reports)
GASTROINTESTINAL HAEMORRHAGE ( 1 FDA reports)
GASTROINTESTINAL HYPOMOTILITY ( 1 FDA reports)
GASTROINTESTINAL MOTILITY DISORDER ( 1 FDA reports)
GENERALISED OEDEMA ( 1 FDA reports)
GINGIVAL BLEEDING ( 1 FDA reports)
GRIP STRENGTH DECREASED ( 1 FDA reports)
HAEMATOCRIT DECREASED ( 1 FDA reports)
HALLUCINATION ( 1 FDA reports)
HEMIPARESIS ( 1 FDA reports)
HEPATORENAL SYNDROME ( 1 FDA reports)
HERPES OESOPHAGITIS ( 1 FDA reports)
HERPES SIMPLEX ( 1 FDA reports)
HERPES ZOSTER ( 1 FDA reports)
HOARSENESS ( 1 FDA reports)
HYPERSOMNIA ( 1 FDA reports)
HYPOCALCAEMIA ( 1 FDA reports)
HYPOGLYCAEMIA NEONATAL ( 1 FDA reports)
HYPOMAGNESAEMIA ( 1 FDA reports)
HYPOVOLAEMIC SHOCK ( 1 FDA reports)
ILEUS ( 1 FDA reports)
INAPPROPRIATE SCHEDULE OF DRUG ADMINISTRATION ( 1 FDA reports)
INCREASED UPPER AIRWAY SECRETION ( 1 FDA reports)
INFECTIOUS PERITONITIS ( 1 FDA reports)
INFUSION RELATED REACTION ( 1 FDA reports)
INITIAL INSOMNIA ( 1 FDA reports)
INJECTION SITE ERYTHEMA ( 1 FDA reports)
INJECTION SITE REACTION ( 1 FDA reports)
INTENTIONAL OVERDOSE ( 1 FDA reports)
INTENTIONAL SELF-INJURY ( 1 FDA reports)
INTESTINAL FISTULA ( 1 FDA reports)
INTESTINAL OBSTRUCTION ( 1 FDA reports)
INTESTINAL OPERATION ( 1 FDA reports)
INTESTINAL PERFORATION ( 1 FDA reports)
INTRACRANIAL VENOUS SINUS THROMBOSIS ( 1 FDA reports)
JEJUNAL PERFORATION ( 1 FDA reports)
LABORATORY TEST INTERFERENCE ( 1 FDA reports)
LARGE INTESTINE PERFORATION ( 1 FDA reports)
LEUKOCYTOCLASTIC VASCULITIS ( 1 FDA reports)
LOCAL SWELLING ( 1 FDA reports)
LUNG INFILTRATION ( 1 FDA reports)
LYMPHOPENIA ( 1 FDA reports)
MALABSORPTION ( 1 FDA reports)
MASS ( 1 FDA reports)
MATERNAL DRUGS AFFECTING FOETUS ( 1 FDA reports)
MELAENA ( 1 FDA reports)
MELANOCYTIC NAEVUS ( 1 FDA reports)
MENTAL DISORDER ( 1 FDA reports)
METASTASES TO PERITONEUM ( 1 FDA reports)
METASTASES TO PLEURA ( 1 FDA reports)
METASTASES TO TESTICLE ( 1 FDA reports)
MICROANGIOPATHY ( 1 FDA reports)
MOOD ALTERED ( 1 FDA reports)
MOUTH HAEMORRHAGE ( 1 FDA reports)
MUSCLE STRAIN ( 1 FDA reports)
MYELODYSPLASTIC SYNDROME TRANSFORMATION ( 1 FDA reports)
MYOPATHY ( 1 FDA reports)
NASAL SEPTUM DISORDER ( 1 FDA reports)
NEONATAL RESPIRATORY DISTRESS SYNDROME ( 1 FDA reports)
NEOPLASM ( 1 FDA reports)
NEOPLASM MALIGNANT ( 1 FDA reports)
NEOPLASM PROGRESSION ( 1 FDA reports)
NERVOUSNESS ( 1 FDA reports)
NEUROPATHY ( 1 FDA reports)
NEUTROPHIL COUNT DECREASED ( 1 FDA reports)
NEUTROPHIL PERCENTAGE DECREASED ( 1 FDA reports)
NO THERAPEUTIC RESPONSE ( 1 FDA reports)
OEDEMA MOUTH ( 1 FDA reports)
OFF LABEL USE ( 1 FDA reports)
ONYCHOMALACIA ( 1 FDA reports)
OPPORTUNISTIC INFECTION ( 1 FDA reports)
OPTIC NEURITIS ( 1 FDA reports)
ORAL INFECTION ( 1 FDA reports)
ORAL INTAKE REDUCED ( 1 FDA reports)
OSTEOARTHRITIS ( 1 FDA reports)
OSTEOLYSIS ( 1 FDA reports)
PERIPHERAL COLDNESS ( 1 FDA reports)
PERIPHERAL SENSORIMOTOR NEUROPATHY ( 1 FDA reports)
PERITONEAL TUBERCULOSIS ( 1 FDA reports)
PERITONITIS ( 1 FDA reports)
PERSISTENT FOETAL CIRCULATION ( 1 FDA reports)
PETECHIAE ( 1 FDA reports)
PLATELET COUNT ABNORMAL ( 1 FDA reports)
PLATELET COUNT INCREASED ( 1 FDA reports)
PNEUMOCOCCAL INFECTION ( 1 FDA reports)
POLYMENORRHOEA ( 1 FDA reports)
POLYP ( 1 FDA reports)
POST PROCEDURAL COMPLICATION ( 1 FDA reports)
POST PROCEDURAL VOMITING ( 1 FDA reports)
PREMATURE RUPTURE OF MEMBRANES ( 1 FDA reports)
PRINZMETAL ANGINA ( 1 FDA reports)
PROCEDURAL SITE REACTION ( 1 FDA reports)
PROTEIN TOTAL DECREASED ( 1 FDA reports)
PRURITUS GENERALISED ( 1 FDA reports)
PULMONARY FIBROSIS ( 1 FDA reports)
RASH ERYTHEMATOUS ( 1 FDA reports)
RASH PRURITIC ( 1 FDA reports)
RECTAL HAEMORRHAGE ( 1 FDA reports)
RED BLOOD CELL SEDIMENTATION RATE INCREASED ( 1 FDA reports)
RENAL FAILURE CHRONIC ( 1 FDA reports)
RESPIRATORY DEPRESSION ( 1 FDA reports)
RIB FRACTURE ( 1 FDA reports)
SEDATION ( 1 FDA reports)
SHOCK HAEMORRHAGIC ( 1 FDA reports)
SKIN REACTION ( 1 FDA reports)
SLEEP DISORDER ( 1 FDA reports)
SMALL INTESTINAL OBSTRUCTION ( 1 FDA reports)
SNEEZING ( 1 FDA reports)
SPINAL FRACTURE ( 1 FDA reports)
SPINAL OSTEOARTHRITIS ( 1 FDA reports)
SUBILEUS ( 1 FDA reports)
SUICIDAL IDEATION ( 1 FDA reports)
SUPRAVENTRICULAR TACHYCARDIA ( 1 FDA reports)
SWELLING FACE ( 1 FDA reports)
SYNCOPE ( 1 FDA reports)
SYNOVITIS ( 1 FDA reports)
TETANY ( 1 FDA reports)
THORACIC HAEMORRHAGE ( 1 FDA reports)
THROAT TIGHTNESS ( 1 FDA reports)
THROMBOCYTOPENIC PURPURA ( 1 FDA reports)
THROMBOPHLEBITIS ( 1 FDA reports)
THYROID DISORDER ( 1 FDA reports)
TOBACCO USER ( 1 FDA reports)
TONIC CONVULSION ( 1 FDA reports)
TRANSPLANT FAILURE ( 1 FDA reports)
TREATMENT NONCOMPLIANCE ( 1 FDA reports)
TUMOUR LYSIS SYNDROME ( 1 FDA reports)
TUMOUR MARKER INCREASED ( 1 FDA reports)
UPPER LIMB FRACTURE ( 1 FDA reports)
UPPER RESPIRATORY TRACT CONGESTION ( 1 FDA reports)
URETERIC DIVERSION OPERATION ( 1 FDA reports)
URINE ABNORMALITY ( 1 FDA reports)
VEIN DISORDER ( 1 FDA reports)
WEIGHT DECREASE NEONATAL ( 1 FDA reports)
WEIGHT INCREASED ( 1 FDA reports)
WHITE BLOOD CELL COUNT INCREASED ( 1 FDA reports)

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