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

FEBRILE NEUTROPENIA ( 104 FDA reports)
NEUTROPENIA ( 93 FDA reports)
DIARRHOEA ( 91 FDA reports)
NAUSEA ( 90 FDA reports)
ABDOMINAL PAIN ( 85 FDA reports)
DEHYDRATION ( 67 FDA reports)
VOMITING ( 62 FDA reports)
ANAEMIA ( 60 FDA reports)
INTESTINAL ISCHAEMIA ( 51 FDA reports)
ASTHENIA ( 41 FDA reports)
NEUTROPENIC SEPSIS ( 41 FDA reports)
DISSEMINATED INTRAVASCULAR COAGULATION ( 40 FDA reports)
LARGE INTESTINE PERFORATION ( 40 FDA reports)
PYREXIA ( 40 FDA reports)
PERITONITIS ( 38 FDA reports)
PLEURAL EFFUSION ( 38 FDA reports)
FATIGUE ( 35 FDA reports)
ABDOMINAL SEPSIS ( 32 FDA reports)
CONSTIPATION ( 32 FDA reports)
ENDOTRACHEAL INTUBATION ( 32 FDA reports)
LUNG CANCER METASTATIC ( 32 FDA reports)
PLATELET COUNT DECREASED ( 32 FDA reports)
RENAL FAILURE ACUTE ( 32 FDA reports)
THROMBOCYTOPENIA ( 32 FDA reports)
CHEST PAIN ( 30 FDA reports)
DYSPNOEA ( 28 FDA reports)
MUCOSAL INFLAMMATION ( 28 FDA reports)
DIZZINESS ( 27 FDA reports)
INFECTIOUS PERITONITIS ( 27 FDA reports)
HYPOKALAEMIA ( 26 FDA reports)
HYPONATRAEMIA ( 25 FDA reports)
LEUKOPENIA ( 25 FDA reports)
GENERAL PHYSICAL HEALTH DETERIORATION ( 24 FDA reports)
WHITE BLOOD CELL COUNT DECREASED ( 24 FDA reports)
ABDOMINAL PAIN UPPER ( 23 FDA reports)
ATRIAL FIBRILLATION ( 21 FDA reports)
DYSPHAGIA ( 20 FDA reports)
HAEMOGLOBIN DECREASED ( 20 FDA reports)
PAIN ( 20 FDA reports)
MALAISE ( 19 FDA reports)
RASH ( 19 FDA reports)
SOMNOLENCE ( 19 FDA reports)
STAPHYLOCOCCAL INFECTION ( 19 FDA reports)
BACK PAIN ( 18 FDA reports)
BONE PAIN ( 18 FDA reports)
HEADACHE ( 18 FDA reports)
HYPOMAGNESAEMIA ( 18 FDA reports)
NEUTROPHIL COUNT DECREASED ( 18 FDA reports)
PNEUMONIA ( 18 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 17 FDA reports)
CONFUSIONAL STATE ( 17 FDA reports)
DEATH ( 17 FDA reports)
DECREASED APPETITE ( 17 FDA reports)
PULMONARY EMBOLISM ( 17 FDA reports)
SMALL INTESTINAL OBSTRUCTION ( 17 FDA reports)
BLOOD ALKALINE PHOSPHATASE INCREASED ( 16 FDA reports)
ERYTHEMA ( 16 FDA reports)
NEOPLASM MALIGNANT ( 16 FDA reports)
SEPTIC SHOCK ( 16 FDA reports)
DEEP VEIN THROMBOSIS ( 15 FDA reports)
DUODENAL ULCER ( 15 FDA reports)
LYMPHADENOPATHY ( 15 FDA reports)
PHLEBITIS ( 15 FDA reports)
RENAL FAILURE ( 15 FDA reports)
STOMATITIS ( 15 FDA reports)
SWOLLEN TONGUE ( 15 FDA reports)
ARTHRALGIA ( 14 FDA reports)
HICCUPS ( 14 FDA reports)
ILEUS ( 14 FDA reports)
PAIN IN JAW ( 14 FDA reports)
SWELLING ( 14 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 13 FDA reports)
DEPRESSION ( 13 FDA reports)
ELECTROCARDIOGRAM T WAVE INVERSION ( 13 FDA reports)
FLUSHING ( 13 FDA reports)
HYPERTENSION ( 13 FDA reports)
INFLUENZA ( 13 FDA reports)
SEPSIS ( 13 FDA reports)
SINUSITIS ( 13 FDA reports)
ALOPECIA ( 12 FDA reports)
CELLULITIS ( 12 FDA reports)
CYSTITIS HAEMORRHAGIC ( 12 FDA reports)
DRUG INTERACTION ( 12 FDA reports)
HYPERGLYCAEMIA ( 12 FDA reports)
HYPOCALCAEMIA ( 12 FDA reports)
HYPOTENSION ( 12 FDA reports)
MUSCLE TWITCHING ( 12 FDA reports)
OEDEMA PERIPHERAL ( 12 FDA reports)
SMALL INTESTINAL HAEMORRHAGE ( 12 FDA reports)
BLOOD SODIUM DECREASED ( 11 FDA reports)
BREAST LUMP REMOVAL ( 11 FDA reports)
BRONCHITIS ( 11 FDA reports)
CARDIAC FAILURE ( 11 FDA reports)
CHEST DISCOMFORT ( 11 FDA reports)
CONVULSION ( 11 FDA reports)
INTERVERTEBRAL DISC PROTRUSION ( 11 FDA reports)
LEFT VENTRICULAR DYSFUNCTION ( 11 FDA reports)
LYMPHADENECTOMY ( 11 FDA reports)
LYMPHOCYTE COUNT DECREASED ( 11 FDA reports)
LYMPHOEDEMA ( 11 FDA reports)
MIGRAINE ( 11 FDA reports)
NON-HODGKIN'S LYMPHOMA ( 11 FDA reports)
ORAL CANDIDIASIS ( 11 FDA reports)
PNEUMONIA STAPHYLOCOCCAL ( 11 FDA reports)
SEBACEOUS GLAND DISORDER ( 11 FDA reports)
SPINAL CORD COMPRESSION ( 11 FDA reports)
SPINAL OSTEOARTHRITIS ( 11 FDA reports)
SUPRAVENTRICULAR TACHYCARDIA ( 11 FDA reports)
ANAPHYLACTIC REACTION ( 10 FDA reports)
ANXIETY ( 10 FDA reports)
BLOOD CREATININE INCREASED ( 10 FDA reports)
NEOPLASM PROGRESSION ( 10 FDA reports)
PAIN IN EXTREMITY ( 10 FDA reports)
PALMAR-PLANTAR ERYTHRODYSAESTHESIA SYNDROME ( 10 FDA reports)
SPLENIC INFARCTION ( 10 FDA reports)
SYNCOPE ( 10 FDA reports)
URTICARIA ( 10 FDA reports)
WEIGHT DECREASED ( 10 FDA reports)
ASCITES ( 9 FDA reports)
BODY TEMPERATURE INCREASED ( 9 FDA reports)
DIVERTICULAR PERFORATION ( 9 FDA reports)
DIVERTICULUM INTESTINAL HAEMORRHAGIC ( 9 FDA reports)
NECK PAIN ( 9 FDA reports)
RENAL IMPAIRMENT ( 9 FDA reports)
RESPIRATORY TRACT INFECTION ( 9 FDA reports)
ALTERED STATE OF CONSCIOUSNESS ( 8 FDA reports)
DEAFNESS NEUROSENSORY ( 8 FDA reports)
DELIRIUM ( 8 FDA reports)
HYPERHIDROSIS ( 8 FDA reports)
JUGULAR VEIN THROMBOSIS ( 8 FDA reports)
PANCYTOPENIA ( 8 FDA reports)
PNEUMONITIS ( 8 FDA reports)
PROTEIN TOTAL DECREASED ( 8 FDA reports)
SCOLIOSIS ( 8 FDA reports)
TACHYCARDIA ( 8 FDA reports)
ANOREXIA ( 7 FDA reports)
ANXIETY DISORDER ( 7 FDA reports)
ARTHRITIS ( 7 FDA reports)
BLOOD CALCIUM DECREASED ( 7 FDA reports)
BLOOD GLUCOSE INCREASED ( 7 FDA reports)
C-REACTIVE PROTEIN INCREASED ( 7 FDA reports)
CHOLELITHIASIS ( 7 FDA reports)
DISEASE PROGRESSION ( 7 FDA reports)
DRUG DEPENDENCE ( 7 FDA reports)
DYSPEPSIA ( 7 FDA reports)
GASTROINTESTINAL HAEMORRHAGE ( 7 FDA reports)
HAEMATOCHEZIA ( 7 FDA reports)
HYPOALBUMINAEMIA ( 7 FDA reports)
INSOMNIA ( 7 FDA reports)
IRRITABILITY ( 7 FDA reports)
KLEBSIELLA INFECTION ( 7 FDA reports)
OESOPHAGITIS ( 7 FDA reports)
PULMONARY OEDEMA ( 7 FDA reports)
RECTAL HAEMORRHAGE ( 7 FDA reports)
RESPIRATORY FAILURE ( 7 FDA reports)
RHINORRHOEA ( 7 FDA reports)
SPINAL CORD INJURY ( 7 FDA reports)
SWELLING FACE ( 7 FDA reports)
THROMBOSIS ( 7 FDA reports)
APHASIA ( 6 FDA reports)
APLASIA ( 6 FDA reports)
BILIARY DYSKINESIA ( 6 FDA reports)
BLOOD POTASSIUM DECREASED ( 6 FDA reports)
CARDIO-RESPIRATORY ARREST ( 6 FDA reports)
CHILLS ( 6 FDA reports)
DISORIENTATION ( 6 FDA reports)
DIVERTICULITIS ( 6 FDA reports)
DRUG INEFFECTIVE ( 6 FDA reports)
EMBOLISM ( 6 FDA reports)
ENTERITIS ( 6 FDA reports)
FANCONI SYNDROME ( 6 FDA reports)
GALLBLADDER DISORDER ( 6 FDA reports)
GASTROINTESTINAL NECROSIS ( 6 FDA reports)
GASTROINTESTINAL PERFORATION ( 6 FDA reports)
HAEMORRHAGIC ANAEMIA ( 6 FDA reports)
HOSPITALISATION ( 6 FDA reports)
HYPOAESTHESIA ( 6 FDA reports)
LARGE INTESTINAL HAEMORRHAGE ( 6 FDA reports)
LOSS OF CONSCIOUSNESS ( 6 FDA reports)
LOWER RESPIRATORY TRACT INFECTION ( 6 FDA reports)
MAMMOPLASTY ( 6 FDA reports)
OVARIAN CANCER ( 6 FDA reports)
PARAESTHESIA ( 6 FDA reports)
PERONEAL NERVE PALSY ( 6 FDA reports)
PRESYNCOPE ( 6 FDA reports)
PROCEDURAL PAIN ( 6 FDA reports)
RED BLOOD CELL COUNT DECREASED ( 6 FDA reports)
SYNCOPE VASOVAGAL ( 6 FDA reports)
WHITE BLOOD CELL COUNT INCREASED ( 6 FDA reports)
ABDOMINAL DISCOMFORT ( 5 FDA reports)
ACTIVITIES OF DAILY LIVING IMPAIRED ( 5 FDA reports)
BLOOD BILIRUBIN INCREASED ( 5 FDA reports)
BLOOD CULTURE POSITIVE ( 5 FDA reports)
BRONCHOPNEUMONIA ( 5 FDA reports)
CARDIAC FAILURE CONGESTIVE ( 5 FDA reports)
COMA ( 5 FDA reports)
COUGH ( 5 FDA reports)
DYSGEUSIA ( 5 FDA reports)
FACIAL PAIN ( 5 FDA reports)
FAECALOMA ( 5 FDA reports)
FLANK PAIN ( 5 FDA reports)
FUNGAL INFECTION ( 5 FDA reports)
HAEMATOCRIT DECREASED ( 5 FDA reports)
HAEMOLYTIC ANAEMIA ( 5 FDA reports)
HYPERTHERMIA ( 5 FDA reports)
ISCHAEMIC STROKE ( 5 FDA reports)
JOINT SWELLING ( 5 FDA reports)
LIVER FUNCTION TEST ABNORMAL ( 5 FDA reports)
MENTAL STATUS CHANGES ( 5 FDA reports)
METABOLIC ACIDOSIS ( 5 FDA reports)
NEUROPATHY PERIPHERAL ( 5 FDA reports)
OFF LABEL USE ( 5 FDA reports)
REVERSIBLE POSTERIOR LEUKOENCEPHALOPATHY SYNDROME ( 5 FDA reports)
TOXICITY TO VARIOUS AGENTS ( 5 FDA reports)
URINARY TRACT INFECTION ( 5 FDA reports)
ABDOMINAL DISTENSION ( 4 FDA reports)
ABDOMINAL PAIN LOWER ( 4 FDA reports)
ABDOMINAL TENDERNESS ( 4 FDA reports)
ABSCESS ( 4 FDA reports)
AMAUROSIS ( 4 FDA reports)
APPENDICITIS ( 4 FDA reports)
ARRHYTHMIA ( 4 FDA reports)
ATRIAL FLUTTER ( 4 FDA reports)
BILE DUCT STENOSIS ( 4 FDA reports)
BLOOD URINE PRESENT ( 4 FDA reports)
BODY TEMPERATURE DECREASED ( 4 FDA reports)
CIRCULATORY COLLAPSE ( 4 FDA reports)
CLOSTRIDIAL INFECTION ( 4 FDA reports)
CREPITATIONS ( 4 FDA reports)
DEVICE RELATED INFECTION ( 4 FDA reports)
DRUG LEVEL INCREASED ( 4 FDA reports)
ENTEROCOLITIS INFECTIOUS ( 4 FDA reports)
FLATULENCE ( 4 FDA reports)
GLARE ( 4 FDA reports)
GLOMERULAR FILTRATION RATE DECREASED ( 4 FDA reports)
GLUCOSE URINE PRESENT ( 4 FDA reports)
HALLUCINATION, AUDITORY ( 4 FDA reports)
HEART RATE INCREASED ( 4 FDA reports)
HYDRONEPHROSIS ( 4 FDA reports)
HYPERAMYLASAEMIA ( 4 FDA reports)
HYPERBILIRUBINAEMIA ( 4 FDA reports)
HYPOGLYCAEMIA ( 4 FDA reports)
HYPOPHAGIA ( 4 FDA reports)
HYPOTHYROIDISM ( 4 FDA reports)
IMPAIRED HEALING ( 4 FDA reports)
INAPPROPRIATE ANTIDIURETIC HORMONE SECRETION ( 4 FDA reports)
INTESTINAL PERFORATION ( 4 FDA reports)
INTESTINAL STENOSIS ( 4 FDA reports)
LOBAR PNEUMONIA ( 4 FDA reports)
LOGORRHOEA ( 4 FDA reports)
LUNG INFECTION ( 4 FDA reports)
LYMPH NODE PAIN ( 4 FDA reports)
MESENTERIC OCCLUSION ( 4 FDA reports)
METASTASES TO BONE ( 4 FDA reports)
METASTASES TO LUNG ( 4 FDA reports)
OEDEMA ( 4 FDA reports)
OXYGEN SATURATION DECREASED ( 4 FDA reports)
PORTAL VEIN THROMBOSIS ( 4 FDA reports)
PROTEIN URINE PRESENT ( 4 FDA reports)
PULMONARY HYPERTENSION ( 4 FDA reports)
RECALL PHENOMENON ( 4 FDA reports)
RENAL INFARCT ( 4 FDA reports)
SKIN TOXICITY ( 4 FDA reports)
VASCULITIS ( 4 FDA reports)
ACUTE RESPIRATORY DISTRESS SYNDROME ( 3 FDA reports)
AGITATION ( 3 FDA reports)
APHAGIA ( 3 FDA reports)
AXILLARY MASS ( 3 FDA reports)
AXILLARY PAIN ( 3 FDA reports)
BILE DUCT CANCER ( 3 FDA reports)
BREAST PAIN ( 3 FDA reports)
CANDIDIASIS ( 3 FDA reports)
CANDIDURIA ( 3 FDA reports)
CARDIAC ARREST ( 3 FDA reports)
CEREBROVASCULAR ACCIDENT ( 3 FDA reports)
CHOLANGITIS ( 3 FDA reports)
CLOSTRIDIUM BACTERAEMIA ( 3 FDA reports)
CLOSTRIDIUM DIFFICILE COLITIS ( 3 FDA reports)
COGNITIVE DISORDER ( 3 FDA reports)
COLITIS ( 3 FDA reports)
CONDITION AGGRAVATED ( 3 FDA reports)
DENTAL OPERATION ( 3 FDA reports)
DIALYSIS ( 3 FDA reports)
DISCOMFORT ( 3 FDA reports)
DRUG ERUPTION ( 3 FDA reports)
ENCEPHALOPATHY ( 3 FDA reports)
EPISTAXIS ( 3 FDA reports)
FALL ( 3 FDA reports)
GAMMA-GLUTAMYLTRANSFERASE INCREASED ( 3 FDA reports)
GLOSSODYNIA ( 3 FDA reports)
GRANULOCYTE COUNT DECREASED ( 3 FDA reports)
GRANULOCYTOPENIA ( 3 FDA reports)
HOT FLUSH ( 3 FDA reports)
HYDROURETER ( 3 FDA reports)
HYPERKALAEMIA ( 3 FDA reports)
HYPERSENSITIVITY ( 3 FDA reports)
ICHTHYOSIS ACQUIRED ( 3 FDA reports)
INFUSION RELATED REACTION ( 3 FDA reports)
INJECTION SITE RASH ( 3 FDA reports)
LIPOMA ( 3 FDA reports)
LOCAL SWELLING ( 3 FDA reports)
LOOSE TOOTH ( 3 FDA reports)
LUNG NEOPLASM MALIGNANT ( 3 FDA reports)
LYMPHOPENIA ( 3 FDA reports)
MALIGNANT NEOPLASM PROGRESSION ( 3 FDA reports)
MASTECTOMY ( 3 FDA reports)
MASTICATION DISORDER ( 3 FDA reports)
MEMORY IMPAIRMENT ( 3 FDA reports)
MOUTH ULCERATION ( 3 FDA reports)
NEOPLASM ( 3 FDA reports)
NEPHROTIC SYNDROME ( 3 FDA reports)
NEUTROPHIL COUNT INCREASED ( 3 FDA reports)
OESOPHAGEAL CANDIDIASIS ( 3 FDA reports)
OVARIAN MASS ( 3 FDA reports)
PERFORMANCE STATUS DECREASED ( 3 FDA reports)
PERICARDIAL EFFUSION ( 3 FDA reports)
PHARYNGEAL OEDEMA ( 3 FDA reports)
PLATELET COUNT INCREASED ( 3 FDA reports)
PRODUCTIVE COUGH ( 3 FDA reports)
PSORIASIS ( 3 FDA reports)
PULMONARY ALVEOLAR HAEMORRHAGE ( 3 FDA reports)
RASH ERYTHEMATOUS ( 3 FDA reports)
RASH MACULAR ( 3 FDA reports)
REFUSAL OF TREATMENT BY PATIENT ( 3 FDA reports)
RHABDOMYOLYSIS ( 3 FDA reports)
SUBCUTANEOUS ABSCESS ( 3 FDA reports)
SUDDEN DEATH ( 3 FDA reports)
SUNBURN ( 3 FDA reports)
TERATOMA ( 3 FDA reports)
THROMBOTIC MICROANGIOPATHY ( 3 FDA reports)
TINNITUS ( 3 FDA reports)
TOOTH DISORDER ( 3 FDA reports)
TREMOR ( 3 FDA reports)
TUMOUR EXCISION ( 3 FDA reports)
URINARY HESITATION ( 3 FDA reports)
WOUND ( 3 FDA reports)
ACUTE MYOCARDIAL INFARCTION ( 2 FDA reports)
ACUTE RESPIRATORY FAILURE ( 2 FDA reports)
ADVERSE DRUG REACTION ( 2 FDA reports)
ALPHA HAEMOLYTIC STREPTOCOCCAL INFECTION ( 2 FDA reports)
ANAPHYLACTIC SHOCK ( 2 FDA reports)
ANAPLASTIC LARGE CELL LYMPHOMA T- AND NULL-CELL TYPES ( 2 FDA reports)
ANGINA PECTORIS ( 2 FDA reports)
ANTITHROMBIN III DECREASED ( 2 FDA reports)
AORTIC EMBOLUS ( 2 FDA reports)
ATELECTASIS ( 2 FDA reports)
AUTOIMMUNE THROMBOCYTOPENIA ( 2 FDA reports)
BACTERIAL INFECTION ( 2 FDA reports)
BETA HAEMOLYTIC STREPTOCOCCAL INFECTION ( 2 FDA reports)
BILIARY TRACT DISORDER ( 2 FDA reports)
BLOOD AMYLASE INCREASED ( 2 FDA reports)
BLOOD CHLORIDE DECREASED ( 2 FDA reports)
BLOOD PHOSPHORUS DECREASED ( 2 FDA reports)
BLOOD PRESSURE DECREASED ( 2 FDA reports)
BONE DISORDER ( 2 FDA reports)
BRAIN NEOPLASM ( 2 FDA reports)
CAECITIS ( 2 FDA reports)
CATHETER SITE PAIN ( 2 FDA reports)
CHOLESTASIS ( 2 FDA reports)
CULTURE URINE POSITIVE ( 2 FDA reports)
CYTOMEGALOVIRUS INFECTION ( 2 FDA reports)
DENTAL NECROSIS ( 2 FDA reports)
EMPYEMA ( 2 FDA reports)
ENDOTOXAEMIA ( 2 FDA reports)
ENGRAFT FAILURE ( 2 FDA reports)
FEELING HOT ( 2 FDA reports)
FEMORAL ARTERY EMBOLISM ( 2 FDA reports)
FRACTURE ( 2 FDA reports)
GAIT DISTURBANCE ( 2 FDA reports)
GENERALISED ERYTHEMA ( 2 FDA reports)
GINGIVAL INFECTION ( 2 FDA reports)
HAEMORRHAGIC CEREBRAL INFARCTION ( 2 FDA reports)
HEAD INJURY ( 2 FDA reports)
HEPATITIS CHOLESTATIC ( 2 FDA reports)
HEPATOMEGALY ( 2 FDA reports)
HYPERAMMONAEMIC ENCEPHALOPATHY ( 2 FDA reports)
HYPERMAGNESAEMIA ( 2 FDA reports)
HYPERTENSIVE HEART DISEASE ( 2 FDA reports)
HYPERURICAEMIA ( 2 FDA reports)
HYPOGAMMAGLOBULINAEMIA ( 2 FDA reports)
HYPOPHOSPHATAEMIA ( 2 FDA reports)
HYPOVOLAEMIC SHOCK ( 2 FDA reports)
INFECTION ( 2 FDA reports)
INFLUENZA LIKE ILLNESS ( 2 FDA reports)
INJECTION SITE ERYTHEMA ( 2 FDA reports)
IRON DEFICIENCY ANAEMIA ( 2 FDA reports)
JAUNDICE CHOLESTATIC ( 2 FDA reports)
LACTIC ACIDOSIS ( 2 FDA reports)
LARYNGEAL DISORDER ( 2 FDA reports)
LARYNGEAL OEDEMA ( 2 FDA reports)
LETHARGY ( 2 FDA reports)
LIPASE INCREASED ( 2 FDA reports)
LIVER DISORDER ( 2 FDA reports)
LUNG INFILTRATION ( 2 FDA reports)
LYMPHOCYTOSIS ( 2 FDA reports)
METASTASES TO CENTRAL NERVOUS SYSTEM ( 2 FDA reports)
METASTASES TO LIVER ( 2 FDA reports)
MOUTH HAEMORRHAGE ( 2 FDA reports)
MUSCULAR WEAKNESS ( 2 FDA reports)
MUSCULOSKELETAL PAIN ( 2 FDA reports)
MYALGIA ( 2 FDA reports)
NON-CARDIAC CHEST PAIN ( 2 FDA reports)
OCULAR HYPERAEMIA ( 2 FDA reports)
ORAL PAIN ( 2 FDA reports)
ORTHOSTATIC HYPOTENSION ( 2 FDA reports)
OSTEONECROSIS ( 2 FDA reports)
PALLOR ( 2 FDA reports)
PARAESTHESIA ORAL ( 2 FDA reports)
PERIORBITAL OEDEMA ( 2 FDA reports)
PNEUMOCYSTIS JIROVECI PNEUMONIA ( 2 FDA reports)
PNEUMONIA FUNGAL ( 2 FDA reports)
POST PROCEDURAL COMPLICATION ( 2 FDA reports)
PRIMARY SEQUESTRUM ( 2 FDA reports)
PROTEINURIA ( 2 FDA reports)
PULMONARY FIBROSIS ( 2 FDA reports)
PULSE ABSENT ( 2 FDA reports)
PURPURA ( 2 FDA reports)
RADIATION SKIN INJURY ( 2 FDA reports)
RASH GENERALISED ( 2 FDA reports)
RESTLESSNESS ( 2 FDA reports)
SENSITIVITY OF TEETH ( 2 FDA reports)
SHOCK HAEMORRHAGIC ( 2 FDA reports)
SKIN EXFOLIATION ( 2 FDA reports)
SMALL CELL LUNG CANCER STAGE UNSPECIFIED ( 2 FDA reports)
SOFT TISSUE INFECTION ( 2 FDA reports)
SPEECH DISORDER DEVELOPMENTAL ( 2 FDA reports)
STERNAL FRACTURE ( 2 FDA reports)
THERAPEUTIC RESPONSE DECREASED ( 2 FDA reports)
THROMBOSIS IN DEVICE ( 2 FDA reports)
TINEA PEDIS ( 2 FDA reports)
TOOTH ABSCESS ( 2 FDA reports)
TOOTH DEPOSIT ( 2 FDA reports)
TOOTH EXTRACTION ( 2 FDA reports)
TOOTHACHE ( 2 FDA reports)
TOXIC EPIDERMAL NECROLYSIS ( 2 FDA reports)
TRACHEAL HAEMORRHAGE ( 2 FDA reports)
TRANSAMINASES INCREASED ( 2 FDA reports)
UNEVALUABLE EVENT ( 2 FDA reports)
UPPER GASTROINTESTINAL HAEMORRHAGE ( 2 FDA reports)
VAGUS NERVE DISORDER ( 2 FDA reports)
VENOOCCLUSIVE DISEASE ( 2 FDA reports)
VERTIGO ( 2 FDA reports)
WOUND COMPLICATION ( 2 FDA reports)
ABORTION SPONTANEOUS ( 1 FDA reports)
ACUTE PRERENAL FAILURE ( 1 FDA reports)
AGRANULOCYTOSIS ( 1 FDA reports)
ALANINE AMINOTRANSFERASE ( 1 FDA reports)
ANGIOEDEMA ( 1 FDA reports)
ANGIONEUROTIC OEDEMA ( 1 FDA reports)
ANKLE FRACTURE ( 1 FDA reports)
ANOXIA ( 1 FDA reports)
ANTIPSYCHOTIC DRUG LEVEL INCREASED ( 1 FDA reports)
AORTIC DISSECTION ( 1 FDA reports)
ARTERIAL BYPASS OPERATION ( 1 FDA reports)
ARTERIAL THROMBOSIS LIMB ( 1 FDA reports)
ARTERIOSCLEROSIS ( 1 FDA reports)
ASPIRATION TRACHEAL ABNORMAL ( 1 FDA reports)
BACILLUS INFECTION ( 1 FDA reports)
BACTERIAL TEST POSITIVE ( 1 FDA reports)
BILIARY SEPSIS ( 1 FDA reports)
BLINDNESS UNILATERAL ( 1 FDA reports)
BLOOD ALBUMIN INCREASED ( 1 FDA reports)
BLOOD ELECTROLYTES ABNORMAL ( 1 FDA reports)
BLOOD LACTATE DEHYDROGENASE INCREASED ( 1 FDA reports)
BLOOD MAGNESIUM DECREASED ( 1 FDA reports)
BLOOD OSMOLARITY DECREASED ( 1 FDA reports)
BLOOD PRESSURE IMMEASURABLE ( 1 FDA reports)
BLOOD PRESSURE INCREASED ( 1 FDA reports)
BLOOD PRESSURE SYSTOLIC INCREASED ( 1 FDA reports)
BLOOD UREA INCREASED ( 1 FDA reports)
BONE SWELLING ( 1 FDA reports)
BRAIN MASS ( 1 FDA reports)
BRAIN NATRIURETIC PEPTIDE INCREASED ( 1 FDA reports)
BREAST CANCER ( 1 FDA reports)
BUNDLE BRANCH BLOCK LEFT ( 1 FDA reports)
BUNDLE BRANCH BLOCK RIGHT ( 1 FDA reports)
CARDIAC TAMPONADE ( 1 FDA reports)
CARDIAC VENTRICULAR DISORDER ( 1 FDA reports)
CARDIOMEGALY ( 1 FDA reports)
CARDIOMYOPATHY ( 1 FDA reports)
CARDIOTOXICITY ( 1 FDA reports)
CARDIOVASCULAR DISORDER ( 1 FDA reports)
CATHETER SITE DISCHARGE ( 1 FDA reports)
CATHETER SITE RELATED REACTION ( 1 FDA reports)
CELL DEATH ( 1 FDA reports)
CEREBELLAR SYNDROME ( 1 FDA reports)
CEREBRAL INFARCTION ( 1 FDA reports)
CEREBRAL VENOUS THROMBOSIS ( 1 FDA reports)
CHOKING ( 1 FDA reports)
CHOKING SENSATION ( 1 FDA reports)
CHOLANGITIS SUPPURATIVE ( 1 FDA reports)
CHRONIC OBSTRUCTIVE PULMONARY DISEASE ( 1 FDA reports)
COCCIDIOIDOMYCOSIS ( 1 FDA reports)
COLD SWEAT ( 1 FDA reports)
COLITIS ULCERATIVE ( 1 FDA reports)
COLORECTAL CANCER ( 1 FDA reports)
CONJUNCTIVITIS ( 1 FDA reports)
CULTURE POSITIVE ( 1 FDA reports)
CYANOSIS ( 1 FDA reports)
CYSTITIS ( 1 FDA reports)
CYTOLYTIC HEPATITIS ( 1 FDA reports)
DEAFNESS ( 1 FDA reports)
DELUSION ( 1 FDA reports)
DERMAL CYST ( 1 FDA reports)
DERMATITIS ( 1 FDA reports)
DEVICE MALFUNCTION ( 1 FDA reports)
DILATATION INTRAHEPATIC DUCT ACQUIRED ( 1 FDA reports)
DIPLOPIA ( 1 FDA reports)
DRUG ADMINISTRATION ERROR ( 1 FDA reports)
DRUG DOSE OMISSION ( 1 FDA reports)
DRUG EXPOSURE DURING PREGNANCY ( 1 FDA reports)
DRUG HYPERSENSITIVITY ( 1 FDA reports)
DYSAESTHESIA ( 1 FDA reports)
DYSTONIA ( 1 FDA reports)
EAR PAIN ( 1 FDA reports)
EJECTION FRACTION DECREASED ( 1 FDA reports)
ELECTROCARDIOGRAM POOR R-WAVE PROGRESSION ( 1 FDA reports)
ELECTROCARDIOGRAM QT PROLONGED ( 1 FDA reports)
ELECTROLYTE IMBALANCE ( 1 FDA reports)
ENDARTERECTOMY ( 1 FDA reports)
ENDOCARDITIS ( 1 FDA reports)
ENTEROCOCCAL BACTERAEMIA ( 1 FDA reports)
EPILEPSY ( 1 FDA reports)
EROSIVE OESOPHAGITIS ( 1 FDA reports)
ESCHERICHIA INFECTION ( 1 FDA reports)
ESCHERICHIA URINARY TRACT INFECTION ( 1 FDA reports)
EYE PAIN ( 1 FDA reports)
EYELID PTOSIS ( 1 FDA reports)
FEBRILE INFECTION ( 1 FDA reports)
FEELING COLD ( 1 FDA reports)
FEMORAL ARTERY OCCLUSION ( 1 FDA reports)
FIBRIN D DIMER INCREASED ( 1 FDA reports)
FLUID REPLACEMENT ( 1 FDA reports)
FLUID RETENTION ( 1 FDA reports)
FUNGUS SPUTUM TEST POSITIVE ( 1 FDA reports)
GASTRIC DILATATION ( 1 FDA reports)
GASTRIC DISORDER ( 1 FDA reports)
GASTRIC HAEMORRHAGE ( 1 FDA reports)
GASTRIC ULCER ( 1 FDA reports)
GASTROINTESTINAL ANASTOMOTIC LEAK ( 1 FDA reports)
GASTROINTESTINAL DISORDER ( 1 FDA reports)
GASTROINTESTINAL OBSTRUCTION ( 1 FDA reports)
GERM CELL CANCER ( 1 FDA reports)
GINGIVAL BLEEDING ( 1 FDA reports)
GLYCOSYLATED HAEMOGLOBIN INCREASED ( 1 FDA reports)
GOITRE ( 1 FDA reports)
GRAND MAL CONVULSION ( 1 FDA reports)
GRANULOCYTOSIS ( 1 FDA reports)
HAEMODIALYSIS ( 1 FDA reports)
HAEMODYNAMIC INSTABILITY ( 1 FDA reports)
HAEMOGLOBIN ( 1 FDA reports)
HAEMOLYTIC URAEMIC SYNDROME ( 1 FDA reports)
HAEMOPTYSIS ( 1 FDA reports)
HAEMORRHOIDAL HAEMORRHAGE ( 1 FDA reports)
HALLUCINATION, TACTILE ( 1 FDA reports)
HALLUCINATION, VISUAL ( 1 FDA reports)
HEPARIN-INDUCED THROMBOCYTOPENIA ( 1 FDA reports)
HEPATIC ISCHAEMIA ( 1 FDA reports)
HEPATIC LESION ( 1 FDA reports)
HEPATIC TRAUMA ( 1 FDA reports)
HEPATITIS ( 1 FDA reports)
HYPOAESTHESIA FACIAL ( 1 FDA reports)
IATROGENIC INJURY ( 1 FDA reports)
IIIRD NERVE PARALYSIS ( 1 FDA reports)
ILIAC ARTERY OCCLUSION ( 1 FDA reports)
INCONTINENCE ( 1 FDA reports)
INFLAMMATION ( 1 FDA reports)
INJURY ( 1 FDA reports)
INJURY ASSOCIATED WITH DEVICE ( 1 FDA reports)
INTERMITTENT CLAUDICATION ( 1 FDA reports)
INTERSTITIAL LUNG DISEASE ( 1 FDA reports)
INTERVERTEBRAL DISC DEGENERATION ( 1 FDA reports)
INTRACARDIAC MASS ( 1 FDA reports)
KIDNEY FIBROSIS ( 1 FDA reports)
LABORATORY TEST INTERFERENCE ( 1 FDA reports)
LACRIMATION INCREASED ( 1 FDA reports)
LACTOBACILLUS TEST POSITIVE ( 1 FDA reports)
LERICHE SYNDROME ( 1 FDA reports)
LIPASE DECREASED ( 1 FDA reports)
LUNG ADENOCARCINOMA ( 1 FDA reports)
LYMPHADENITIS ( 1 FDA reports)
LYMPHADENOPATHY MEDIASTINAL ( 1 FDA reports)
LYMPHANGITIS ( 1 FDA reports)
MALNUTRITION ( 1 FDA reports)
MASTOIDITIS ( 1 FDA reports)
MENORRHAGIA ( 1 FDA reports)
METASTASES TO ADRENALS ( 1 FDA reports)
METASTASES TO HEART ( 1 FDA reports)
METASTASES TO LYMPH NODES ( 1 FDA reports)
METASTASIS ( 1 FDA reports)
METASTATIC GASTRIC CANCER ( 1 FDA reports)
MOBILITY DECREASED ( 1 FDA reports)
MONONEUROPATHY MULTIPLEX ( 1 FDA reports)
MOVEMENT DISORDER ( 1 FDA reports)
MUCOSAL HAEMORRHAGE ( 1 FDA reports)
MUCOUS MEMBRANE DISORDER ( 1 FDA reports)
MULTI-ORGAN FAILURE ( 1 FDA reports)
MUSCLE SPASMS ( 1 FDA reports)
MYDRIASIS ( 1 FDA reports)
MYOCARDIAL INFARCTION ( 1 FDA reports)
MYOPATHY ( 1 FDA reports)
NASAL CONGESTION ( 1 FDA reports)
NECROSIS ISCHAEMIC ( 1 FDA reports)
NERVE INJURY ( 1 FDA reports)
NERVOUS SYSTEM DISORDER ( 1 FDA reports)
NEUROENDOCRINE TUMOUR ( 1 FDA reports)
NON-SMALL CELL LUNG CANCER ( 1 FDA reports)
NUCLEAR MAGNETIC RESONANCE IMAGING BRAIN ABNORMAL ( 1 FDA reports)
OBSTRUCTION ( 1 FDA reports)
ODYNOPHAGIA ( 1 FDA reports)
OESOPHAGEAL ULCER ( 1 FDA reports)
OPTIC NERVE INFARCTION ( 1 FDA reports)
PALPITATIONS ( 1 FDA reports)
PANCREATIC CARCINOMA ( 1 FDA reports)
PANCREATIC CARCINOMA METASTATIC ( 1 FDA reports)
PANCREATIC PSEUDOCYST ( 1 FDA reports)
PANCREATITIS ( 1 FDA reports)
PANIC ATTACK ( 1 FDA reports)
PARANEOPLASTIC SYNDROME ( 1 FDA reports)
PELVIC PAIN ( 1 FDA reports)
PERICARDITIS ( 1 FDA reports)
PERIPHERAL COLDNESS ( 1 FDA reports)
PERIPHERAL EMBOLISM ( 1 FDA reports)
PERIPHERAL ISCHAEMIA ( 1 FDA reports)
PERIPHERAL REVASCULARISATION ( 1 FDA reports)
PHARYNGEAL HAEMATOMA ( 1 FDA reports)
PHARYNGEAL INFLAMMATION ( 1 FDA reports)
PHOTOSENSITIVITY REACTION ( 1 FDA reports)
PNEUMONIA KLEBSIELLA ( 1 FDA reports)
PREGNANCY OF PARTNER ( 1 FDA reports)
PROCEDURAL COMPLICATION ( 1 FDA reports)
PRODUCT CONTAMINATION MICROBIAL ( 1 FDA reports)
PROGRESSIVE MULTIFOCAL LEUKOENCEPHALOPATHY ( 1 FDA reports)
PROTEIN TOTAL INCREASED ( 1 FDA reports)
PRURITUS ( 1 FDA reports)
PULMONARY HILUM MASS ( 1 FDA reports)
PULMONARY RENAL SYNDROME ( 1 FDA reports)
PULSE PRESSURE DECREASED ( 1 FDA reports)
QRS AXIS ABNORMAL ( 1 FDA reports)
RADIATION MUCOSITIS ( 1 FDA reports)
RADIATION PNEUMONITIS ( 1 FDA reports)
RENAL CYST ( 1 FDA reports)
RENAL TUBULAR DISORDER ( 1 FDA reports)
RENAL TUBULAR NECROSIS ( 1 FDA reports)
RESPIRATORY ARREST ( 1 FDA reports)
RESPIRATORY DISORDER ( 1 FDA reports)
RESPIRATORY TRACT CONGESTION ( 1 FDA reports)
RETCHING ( 1 FDA reports)
SARCOMA METASTATIC ( 1 FDA reports)
SENSATION OF HEAVINESS ( 1 FDA reports)
SENSE OF OPPRESSION ( 1 FDA reports)
SERUM SICKNESS ( 1 FDA reports)
SINUS DISORDER ( 1 FDA reports)
SINUS TACHYCARDIA ( 1 FDA reports)
SKIN EROSION ( 1 FDA reports)
SKIN HAEMORRHAGE ( 1 FDA reports)
SKIN TURGOR DECREASED ( 1 FDA reports)
SKIN ULCER ( 1 FDA reports)
SPUTUM CULTURE POSITIVE ( 1 FDA reports)
SPUTUM INCREASED ( 1 FDA reports)
STEVENS-JOHNSON SYNDROME ( 1 FDA reports)
STOMACH MASS ( 1 FDA reports)
STREPTOCOCCAL INFECTION ( 1 FDA reports)
SUPERINFECTION ( 1 FDA reports)
SUPRAVENTRICULAR EXTRASYSTOLES ( 1 FDA reports)
SURGERY ( 1 FDA reports)
SURGICAL PROCEDURE REPEATED ( 1 FDA reports)
THERAPY REGIMEN CHANGED ( 1 FDA reports)
THROAT TIGHTNESS ( 1 FDA reports)
THROMBOEMBOLECTOMY ( 1 FDA reports)
THROMBOTIC THROMBOCYTOPENIC PURPURA ( 1 FDA reports)
THYROIDITIS ( 1 FDA reports)
TRANSFUSION ( 1 FDA reports)
ULTRASOUND ABDOMEN ABNORMAL ( 1 FDA reports)
UNRESPONSIVE TO STIMULI ( 1 FDA reports)
UPPER AIRWAY OBSTRUCTION ( 1 FDA reports)
URINARY TRACT INFECTION PSEUDOMONAL ( 1 FDA reports)
URINE KETONE BODY PRESENT ( 1 FDA reports)
VENOUS THROMBOSIS LIMB ( 1 FDA reports)
VENTRICULAR DYSFUNCTION ( 1 FDA reports)
VISUAL DISTURBANCE ( 1 FDA reports)
WHITE BLOOD CELLS URINE POSITIVE ( 1 FDA reports)
WOUND DEHISCENCE ( 1 FDA reports)

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