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

CHILLS ( 63 FDA reports)
TACHYCARDIA ( 58 FDA reports)
PYREXIA ( 50 FDA reports)
BLOOD CREATININE INCREASED ( 35 FDA reports)
HYPERTENSION ( 35 FDA reports)
RENAL FAILURE ( 27 FDA reports)
THROMBOCYTOPENIA ( 26 FDA reports)
ANAEMIA ( 25 FDA reports)
HYPOTENSION ( 25 FDA reports)
INFUSION RELATED REACTION ( 24 FDA reports)
TACHYPNOEA ( 24 FDA reports)
OXYGEN SATURATION DECREASED ( 23 FDA reports)
BLOOD PRESSURE INCREASED ( 21 FDA reports)
HEART RATE INCREASED ( 20 FDA reports)
RESPIRATORY FAILURE ( 20 FDA reports)
TREMOR ( 19 FDA reports)
HYPOKALAEMIA ( 17 FDA reports)
NEUTROPENIA ( 17 FDA reports)
RENAL IMPAIRMENT ( 17 FDA reports)
FEBRILE NEUTROPENIA ( 16 FDA reports)
PANCYTOPENIA ( 16 FDA reports)
RASH ( 16 FDA reports)
SEPSIS ( 16 FDA reports)
BLOOD BILIRUBIN INCREASED ( 15 FDA reports)
BLOOD GLUCOSE INCREASED ( 15 FDA reports)
DYSPNOEA ( 15 FDA reports)
MULTI-ORGAN FAILURE ( 15 FDA reports)
RESPIRATORY DISTRESS ( 15 FDA reports)
PNEUMONIA ( 14 FDA reports)
BLOOD UREA INCREASED ( 13 FDA reports)
CONDITION AGGRAVATED ( 13 FDA reports)
DIARRHOEA ( 13 FDA reports)
BRONCHOPULMONARY ASPERGILLOSIS ( 12 FDA reports)
PLATELET COUNT DECREASED ( 12 FDA reports)
BLOOD POTASSIUM DECREASED ( 11 FDA reports)
HYPERBILIRUBINAEMIA ( 11 FDA reports)
PULMONARY EMBOLISM ( 11 FDA reports)
RENAL FAILURE ACUTE ( 11 FDA reports)
ACIDOSIS ( 10 FDA reports)
BODY TEMPERATURE INCREASED ( 10 FDA reports)
DRUG INEFFECTIVE ( 10 FDA reports)
OEDEMA PERIPHERAL ( 10 FDA reports)
RESPIRATORY RATE INCREASED ( 10 FDA reports)
BONE MARROW DISORDER ( 9 FDA reports)
CARDIAC ARREST ( 9 FDA reports)
CONFUSIONAL STATE ( 9 FDA reports)
CYANOSIS ( 9 FDA reports)
GRAFT VERSUS HOST DISEASE ( 9 FDA reports)
NAUSEA ( 9 FDA reports)
AGITATION ( 8 FDA reports)
BLOOD PRESSURE DECREASED ( 8 FDA reports)
BLOOD SODIUM DECREASED ( 8 FDA reports)
COMA ( 8 FDA reports)
CONVULSION ( 8 FDA reports)
DEEP VEIN THROMBOSIS ( 8 FDA reports)
DEPRESSED LEVEL OF CONSCIOUSNESS ( 8 FDA reports)
HAEMOGLOBIN DECREASED ( 8 FDA reports)
HYPOXIA ( 8 FDA reports)
SEPTIC SHOCK ( 8 FDA reports)
THERAPEUTIC PRODUCT CONTAMINATION ( 8 FDA reports)
WHEEZING ( 8 FDA reports)
WHITE BLOOD CELL COUNT DECREASED ( 8 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 7 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 7 FDA reports)
ATRIAL FIBRILLATION ( 7 FDA reports)
BLOOD ALKALINE PHOSPHATASE INCREASED ( 7 FDA reports)
GENERAL PHYSICAL HEALTH DETERIORATION ( 7 FDA reports)
MUCOSAL INFLAMMATION ( 7 FDA reports)
NEPHROGENIC DIABETES INSIPIDUS ( 7 FDA reports)
PLEURAL EFFUSION ( 7 FDA reports)
PULMONARY OEDEMA ( 7 FDA reports)
SHOCK ( 7 FDA reports)
ASPERGILLOSIS ( 6 FDA reports)
ENTEROCOCCAL INFECTION ( 6 FDA reports)
HEADACHE ( 6 FDA reports)
HEPATOSPLENOMEGALY ( 6 FDA reports)
LIVER DISORDER ( 6 FDA reports)
PNEUMONIA FUNGAL ( 6 FDA reports)
ACUTE RESPIRATORY FAILURE ( 5 FDA reports)
ASCITES ( 5 FDA reports)
BLOOD ALBUMIN DECREASED ( 5 FDA reports)
BLOOD BICARBONATE DECREASED ( 5 FDA reports)
BRADYCARDIA ( 5 FDA reports)
BRONCHOSPASM ( 5 FDA reports)
CANDIDIASIS ( 5 FDA reports)
CARDIO-RESPIRATORY ARREST ( 5 FDA reports)
DIALYSIS ( 5 FDA reports)
DISEASE PROGRESSION ( 5 FDA reports)
FLUID OVERLOAD ( 5 FDA reports)
FUNGAL INFECTION ( 5 FDA reports)
GASTROINTESTINAL HAEMORRHAGE ( 5 FDA reports)
HYPERVENTILATION ( 5 FDA reports)
LYMPHADENOPATHY ( 5 FDA reports)
METABOLIC ACIDOSIS ( 5 FDA reports)
NEUROTOXICITY ( 5 FDA reports)
PERICARDIAL EFFUSION ( 5 FDA reports)
PERIPHERAL COLDNESS ( 5 FDA reports)
PROTEIN TOTAL DECREASED ( 5 FDA reports)
SINUS TACHYCARDIA ( 5 FDA reports)
WEIGHT INCREASED ( 5 FDA reports)
ABDOMINAL PAIN ( 4 FDA reports)
ACTIVATED PARTIAL THROMBOPLASTIN TIME PROLONGED ( 4 FDA reports)
ACUTE GRAFT VERSUS HOST DISEASE IN LIVER ( 4 FDA reports)
ACUTE MYOCARDIAL INFARCTION ( 4 FDA reports)
ACUTE RESPIRATORY DISTRESS SYNDROME ( 4 FDA reports)
ASTHENIA ( 4 FDA reports)
BACTERIAL INFECTION ( 4 FDA reports)
BILIRUBIN CONJUGATED INCREASED ( 4 FDA reports)
BLOOD CHLORIDE INCREASED ( 4 FDA reports)
BLOOD CULTURE POSITIVE ( 4 FDA reports)
BLOOD SODIUM INCREASED ( 4 FDA reports)
CHEST PAIN ( 4 FDA reports)
DEATH ( 4 FDA reports)
DRUG RESISTANCE ( 4 FDA reports)
FATIGUE ( 4 FDA reports)
HYPERAMYLASAEMIA ( 4 FDA reports)
HYPERHIDROSIS ( 4 FDA reports)
HYPERKALAEMIA ( 4 FDA reports)
HYPOMAGNESAEMIA ( 4 FDA reports)
LUNG CONSOLIDATION ( 4 FDA reports)
MENTAL STATUS CHANGES ( 4 FDA reports)
NEPHROPATHY TOXIC ( 4 FDA reports)
NO THERAPEUTIC RESPONSE ( 4 FDA reports)
PCO2 DECREASED ( 4 FDA reports)
PERIPHERAL MOTOR NEUROPATHY ( 4 FDA reports)
PHARMACEUTICAL PRODUCT COMPLAINT ( 4 FDA reports)
RALES ( 4 FDA reports)
SOMNOLENCE ( 4 FDA reports)
STAPHYLOCOCCAL BACTERAEMIA ( 4 FDA reports)
THERAPY NON-RESPONDER ( 4 FDA reports)
URINARY TRACT INFECTION ENTEROCOCCAL ( 4 FDA reports)
VENTRICULAR EXTRASYSTOLES ( 4 FDA reports)
VENTRICULAR FIBRILLATION ( 4 FDA reports)
ABDOMINAL DISTENSION ( 3 FDA reports)
ACQUIRED IMMUNODEFICIENCY SYNDROME ( 3 FDA reports)
ACUTE PULMONARY OEDEMA ( 3 FDA reports)
BLOOD CREATINE INCREASED ( 3 FDA reports)
CARDIAC DEATH ( 3 FDA reports)
CARDIAC FAILURE CONGESTIVE ( 3 FDA reports)
CARDIAC TAMPONADE ( 3 FDA reports)
CATHETER RELATED COMPLICATION ( 3 FDA reports)
CYTOMEGALOVIRUS INFECTION ( 3 FDA reports)
DISEASE RECURRENCE ( 3 FDA reports)
DIZZINESS ( 3 FDA reports)
DRUG HYPERSENSITIVITY ( 3 FDA reports)
DRUG INTERACTION ( 3 FDA reports)
ELECTROMECHANICAL DISSOCIATION ( 3 FDA reports)
FEELING COLD ( 3 FDA reports)
GAMMA-GLUTAMYLTRANSFERASE INCREASED ( 3 FDA reports)
HAEMATOCRIT DECREASED ( 3 FDA reports)
HAEMODYNAMIC INSTABILITY ( 3 FDA reports)
HEPATIC FAILURE ( 3 FDA reports)
HERPES VIRUS INFECTION ( 3 FDA reports)
HYPERREFLEXIA ( 3 FDA reports)
HYPOGEUSIA ( 3 FDA reports)
ILEUS ( 3 FDA reports)
ILEUS PARALYTIC ( 3 FDA reports)
INFECTION ( 3 FDA reports)
LIVER FUNCTION TEST ABNORMAL ( 3 FDA reports)
LUNG DISORDER ( 3 FDA reports)
LUNG INFECTION ( 3 FDA reports)
MECHANICAL VENTILATION ( 3 FDA reports)
METRORRHAGIA ( 3 FDA reports)
MUCORMYCOSIS ( 3 FDA reports)
PAIN IN EXTREMITY ( 3 FDA reports)
PETECHIAE ( 3 FDA reports)
PROTHROMBIN TIME PROLONGED ( 3 FDA reports)
PSEUDOMONAL BACTERAEMIA ( 3 FDA reports)
PULMONARY MYCOSIS ( 3 FDA reports)
RESPIRATORY DISORDER ( 3 FDA reports)
RHABDOMYOLYSIS ( 3 FDA reports)
SEPSIS SYNDROME ( 3 FDA reports)
SKIN DISORDER ( 3 FDA reports)
STAPHYLOCOCCAL INFECTION ( 3 FDA reports)
THERAPEUTIC RESPONSE DECREASED ( 3 FDA reports)
URINE OUTPUT DECREASED ( 3 FDA reports)
VISION BLURRED ( 3 FDA reports)
VOMITING ( 3 FDA reports)
ACUTE MYELOID LEUKAEMIA ( 2 FDA reports)
ALOPECIA ( 2 FDA reports)
AMAUROSIS ( 2 FDA reports)
ANAPHYLACTIC REACTION ( 2 FDA reports)
APLASTIC ANAEMIA ( 2 FDA reports)
ATELECTASIS ( 2 FDA reports)
AUTONOMIC NERVOUS SYSTEM IMBALANCE ( 2 FDA reports)
BLINDNESS ( 2 FDA reports)
BLOOD BILIRUBIN ABNORMAL ( 2 FDA reports)
BLOOD CALCIUM DECREASED ( 2 FDA reports)
BLOOD LACTATE DEHYDROGENASE INCREASED ( 2 FDA reports)
BLOOD PRESSURE SYSTOLIC DECREASED ( 2 FDA reports)
BRADYPNOEA ( 2 FDA reports)
BRAIN MASS ( 2 FDA reports)
CARDIOMEGALY ( 2 FDA reports)
CARDIOPULMONARY FAILURE ( 2 FDA reports)
CARDIOVASCULAR DISORDER ( 2 FDA reports)
CENTRAL LINE INFECTION ( 2 FDA reports)
CEREBRAL DISORDER ( 2 FDA reports)
CEREBRAL INFARCTION ( 2 FDA reports)
CEREBRAL TOXOPLASMOSIS ( 2 FDA reports)
CEREBROVASCULAR ACCIDENT ( 2 FDA reports)
CHEST DISCOMFORT ( 2 FDA reports)
CHOLESTASIS ( 2 FDA reports)
CHRONIC OBSTRUCTIVE PULMONARY DISEASE ( 2 FDA reports)
COAGULOPATHY ( 2 FDA reports)
COUGH ( 2 FDA reports)
DEAFNESS ( 2 FDA reports)
DEHYDRATION ( 2 FDA reports)
DIABETES INSIPIDUS ( 2 FDA reports)
DISEASE COMPLICATION ( 2 FDA reports)
DRUG LEVEL BELOW THERAPEUTIC ( 2 FDA reports)
DRUG TOXICITY ( 2 FDA reports)
ECCHYMOSIS ( 2 FDA reports)
EJECTION FRACTION DECREASED ( 2 FDA reports)
ELECTROCARDIOGRAM T WAVE ABNORMAL ( 2 FDA reports)
ERYTHEMA ( 2 FDA reports)
ESCHERICHIA BACTERAEMIA ( 2 FDA reports)
EYE INFECTION ( 2 FDA reports)
FAECAL OCCULT BLOOD POSITIVE ( 2 FDA reports)
GASTRITIS ( 2 FDA reports)
GENERALISED OEDEMA ( 2 FDA reports)
GLYCOSURIA ( 2 FDA reports)
HAEMANGIOMA ( 2 FDA reports)
HAEMODIALYSIS ( 2 FDA reports)
HAEMORRHAGE INTRACRANIAL ( 2 FDA reports)
HAEMORRHAGIC DIATHESIS ( 2 FDA reports)
HEART RATE DECREASED ( 2 FDA reports)
HEPATIC ARTERY ANEURYSM ( 2 FDA reports)
HEPATIC ENZYME INCREASED ( 2 FDA reports)
HEPATIC LESION ( 2 FDA reports)
HEPATOMEGALY ( 2 FDA reports)
HYPERGLYCAEMIA ( 2 FDA reports)
HYPERSENSITIVITY ( 2 FDA reports)
HYPERTENSIVE CRISIS ( 2 FDA reports)
HYPONATRAEMIA ( 2 FDA reports)
HYPOTHERMIA ( 2 FDA reports)
INFUSION SITE ERYTHEMA ( 2 FDA reports)
INFUSION SITE SWELLING ( 2 FDA reports)
INSOMNIA ( 2 FDA reports)
ISCHAEMIC HEPATITIS ( 2 FDA reports)
KLEBSIELLA INFECTION ( 2 FDA reports)
LACTIC ACIDOSIS ( 2 FDA reports)
LETHARGY ( 2 FDA reports)
LOSS OF CONSCIOUSNESS ( 2 FDA reports)
LUNG INFILTRATION ( 2 FDA reports)
MALAISE ( 2 FDA reports)
MARKEDLY REDUCED DIETARY INTAKE ( 2 FDA reports)
MEDICATION ERROR ( 2 FDA reports)
MENINGITIS CRYPTOCOCCAL ( 2 FDA reports)
MUSCULAR WEAKNESS ( 2 FDA reports)
MYOPATHY ( 2 FDA reports)
NERVOUS SYSTEM DISORDER ( 2 FDA reports)
NEUROPATHY PERIPHERAL ( 2 FDA reports)
NUCLEAR MAGNETIC RESONANCE IMAGING ABNORMAL ( 2 FDA reports)
NYSTAGMUS ( 2 FDA reports)
OBSTRUCTIVE AIRWAYS DISORDER ( 2 FDA reports)
ORGAN FAILURE ( 2 FDA reports)
PALLOR ( 2 FDA reports)
PARAESTHESIA ( 2 FDA reports)
PATHOGEN RESISTANCE ( 2 FDA reports)
PERICARDITIS ( 2 FDA reports)
PHARYNGEAL OEDEMA ( 2 FDA reports)
PLATELET COUNT INCREASED ( 2 FDA reports)
PNEUMONIA ASPIRATION ( 2 FDA reports)
POOR QUALITY DRUG ADMINISTERED ( 2 FDA reports)
POST PROCEDURAL COMPLICATION ( 2 FDA reports)
PROCTALGIA ( 2 FDA reports)
PULMONARY MASS ( 2 FDA reports)
PUPIL FIXED ( 2 FDA reports)
RESPIRATORY ALKALOSIS ( 2 FDA reports)
RESPIRATORY ARREST ( 2 FDA reports)
RESTLESSNESS ( 2 FDA reports)
RETROPERITONEAL HAEMORRHAGE ( 2 FDA reports)
SHOULDER PAIN ( 2 FDA reports)
SKIN NODULE ( 2 FDA reports)
SPLENOMEGALY ( 2 FDA reports)
SWELLING FACE ( 2 FDA reports)
THROMBOSIS ( 2 FDA reports)
TREATMENT NONCOMPLIANCE ( 2 FDA reports)
UNRESPONSIVE TO PAIN STIMULI ( 2 FDA reports)
UNRESPONSIVE TO VERBAL STIMULI ( 2 FDA reports)
URINARY HESITATION ( 2 FDA reports)
URTICARIA ( 2 FDA reports)
VENTRICULAR DYSFUNCTION ( 2 FDA reports)
VENTRICULAR HYPERTROPHY ( 2 FDA reports)
VENTRICULAR TACHYCARDIA ( 2 FDA reports)
WHITE BLOOD CELL COUNT INCREASED ( 2 FDA reports)
ABDOMINAL PAIN UPPER ( 1 FDA reports)
ABDOMINAL SEPSIS ( 1 FDA reports)
ABNORMAL BEHAVIOUR ( 1 FDA reports)
ACUTE GRAFT VERSUS HOST DISEASE IN INTESTINE ( 1 FDA reports)
ACUTE GRAFT VERSUS HOST DISEASE IN SKIN ( 1 FDA reports)
ACUTE MYELOID LEUKAEMIA RECURRENT ( 1 FDA reports)
ADRENAL INSUFFICIENCY ( 1 FDA reports)
ALTERED STATE OF CONSCIOUSNESS ( 1 FDA reports)
ANEURYSM RUPTURED ( 1 FDA reports)
ANGIONEUROTIC OEDEMA ( 1 FDA reports)
ANGIOPATHY ( 1 FDA reports)
ANOREXIA ( 1 FDA reports)
ANTICONVULSANT DRUG LEVEL BELOW THERAPEUTIC ( 1 FDA reports)
ANURIA ( 1 FDA reports)
ANXIETY ( 1 FDA reports)
APHASIA ( 1 FDA reports)
APLASIA ( 1 FDA reports)
APNOEA ( 1 FDA reports)
APPETITE DISORDER ( 1 FDA reports)
ARRHYTHMIA ( 1 FDA reports)
ARTERIAL ANEURYSM REPAIR ( 1 FDA reports)
ARTERIAL DISORDER ( 1 FDA reports)
ARTERIOSCLEROSIS ( 1 FDA reports)
ARTERIOSCLEROSIS CORONARY ARTERY ( 1 FDA reports)
ARTHRALGIA ( 1 FDA reports)
ASPIRATION TRACHEAL ABNORMAL ( 1 FDA reports)
ATAXIA ( 1 FDA reports)
BACTERAEMIA ( 1 FDA reports)
BACTERIAL SEPSIS ( 1 FDA reports)
BLASTOMYCOSIS ( 1 FDA reports)
BLISTER ( 1 FDA reports)
BLOOD CREATINE PHOSPHOKINASE INCREASED ( 1 FDA reports)
BLOOD CREATININE ABNORMAL ( 1 FDA reports)
BLOOD DISORDER ( 1 FDA reports)
BLOOD FIBRINOGEN DECREASED ( 1 FDA reports)
BLOOD FIBRINOGEN INCREASED ( 1 FDA reports)
BLOOD GASES ABNORMAL ( 1 FDA reports)
BLOOD GLUCOSE ABNORMAL ( 1 FDA reports)
BLOOD PRESSURE ABNORMAL ( 1 FDA reports)
BLOOD PRESSURE DIASTOLIC DECREASED ( 1 FDA reports)
BLOOD PRESSURE SYSTOLIC INCREASED ( 1 FDA reports)
BONE MARROW DEPRESSION ( 1 FDA reports)
BONE MARROW FAILURE ( 1 FDA reports)
BONE MARROW GRANULOMA ( 1 FDA reports)
BONE MARROW TRANSPLANT ( 1 FDA reports)
BOWEL SOUNDS ABNORMAL ( 1 FDA reports)
BRAIN ABSCESS ( 1 FDA reports)
BRAIN DEATH ( 1 FDA reports)
BRAIN HERNIATION ( 1 FDA reports)
BRAIN OEDEMA ( 1 FDA reports)
BRAIN STEM SYNDROME ( 1 FDA reports)
BREAST CANCER ( 1 FDA reports)
BRONCHIAL HAEMORRHAGE ( 1 FDA reports)
CAECITIS ( 1 FDA reports)
CANDIDA PNEUMONIA ( 1 FDA reports)
CARDIAC DISORDER ( 1 FDA reports)
CARDIAC FAILURE ( 1 FDA reports)
CARDIAC MURMUR ( 1 FDA reports)
CARDIOTOXICITY ( 1 FDA reports)
CATHETER RELATED INFECTION ( 1 FDA reports)
CATHETER SEPSIS ( 1 FDA reports)
CEREBRAL ASPERGILLOSIS ( 1 FDA reports)
CEREBRAL FUNGAL INFECTION ( 1 FDA reports)
CHOKING SENSATION ( 1 FDA reports)
CHOROIDAL DETACHMENT ( 1 FDA reports)
CHOROIDAL EFFUSION ( 1 FDA reports)
CHROMOBLASTOMYCOSIS ( 1 FDA reports)
CHRONIC LYMPHOCYTIC LEUKAEMIA TRANSFORMATION ( 1 FDA reports)
CIRCULATORY COLLAPSE ( 1 FDA reports)
CONGESTIVE CARDIOMYOPATHY ( 1 FDA reports)
CONJUNCTIVAL HAEMORRHAGE ( 1 FDA reports)
CONTINUOUS HAEMODIAFILTRATION ( 1 FDA reports)
CORD BLOOD TRANSPLANT THERAPY ( 1 FDA reports)
CORNEAL ABSCESS ( 1 FDA reports)
CORNEAL OPACITY ( 1 FDA reports)
CREATININE RENAL CLEARANCE DECREASED ( 1 FDA reports)
CRYPTOCOCCUS TEST POSITIVE ( 1 FDA reports)
CULTURE POSITIVE ( 1 FDA reports)
CYTOMEGALOVIRUS CHORIORETINITIS ( 1 FDA reports)
CYTOMEGALOVIRUS COLITIS ( 1 FDA reports)
CYTOMEGALOVIRUS OESOPHAGITIS ( 1 FDA reports)
DEAFNESS UNILATERAL ( 1 FDA reports)
DECREASED APPETITE ( 1 FDA reports)
DEPRESSION ( 1 FDA reports)
DILATATION VENTRICULAR ( 1 FDA reports)
DISCOMFORT ( 1 FDA reports)
DISORIENTATION ( 1 FDA reports)
DIZZINESS POSTURAL ( 1 FDA reports)
DRUG ADMINISTRATION ERROR ( 1 FDA reports)
DRUG DISPENSING ERROR ( 1 FDA reports)
DRUG INTOLERANCE ( 1 FDA reports)
DYSARTHRIA ( 1 FDA reports)
DYSGEUSIA ( 1 FDA reports)
ECHOLALIA ( 1 FDA reports)
ELECTROCARDIOGRAM ABNORMAL ( 1 FDA reports)
EMBOLISM ( 1 FDA reports)
EMOTIONAL DISORDER ( 1 FDA reports)
ENCEPHALOPATHY ( 1 FDA reports)
ENDOTRACHEAL INTUBATION ( 1 FDA reports)
ENTEROBACTER INFECTION ( 1 FDA reports)
ENTEROCOCCAL BACTERAEMIA ( 1 FDA reports)
ENTEROCOCCAL SEPSIS ( 1 FDA reports)
ERYTHEMA MULTIFORME ( 1 FDA reports)
EXTRAVASATION ( 1 FDA reports)
EXTREMITY CONTRACTURE ( 1 FDA reports)
EYE DISORDER ( 1 FDA reports)
EYE SWELLING ( 1 FDA reports)
FACE OEDEMA ( 1 FDA reports)
FAT EMBOLISM ( 1 FDA reports)
FIBRIN D DIMER INCREASED ( 1 FDA reports)
FLATULENCE ( 1 FDA reports)
FUNGAEMIA ( 1 FDA reports)
FUNGAL SKIN INFECTION ( 1 FDA reports)
FUNGUS URINE TEST POSITIVE ( 1 FDA reports)
GALLBLADDER NECROSIS ( 1 FDA reports)
GASTRIC DISORDER ( 1 FDA reports)
GASTRIC PERFORATION ( 1 FDA reports)
GASTROINTESTINAL MUCOSITIS ( 1 FDA reports)
GENERALISED ERYTHEMA ( 1 FDA reports)
GLOSSITIS ( 1 FDA reports)
GRAFT VERSUS HOST DISEASE IN LIVER ( 1 FDA reports)
GRANULOMA ( 1 FDA reports)
GRANULOMATOUS LIVER DISEASE ( 1 FDA reports)
GUILLAIN-BARRE SYNDROME ( 1 FDA reports)
HAEMANGIOMA OF LIVER ( 1 FDA reports)
HAEMATEMESIS ( 1 FDA reports)
HAEMATOTOXICITY ( 1 FDA reports)
HAEMOPTYSIS ( 1 FDA reports)
HALLUCINATION ( 1 FDA reports)
HEART SOUNDS ABNORMAL ( 1 FDA reports)
HEART TRANSPLANT REJECTION ( 1 FDA reports)
HEPATIC FUNCTION ABNORMAL ( 1 FDA reports)
HEPATORENAL SYNDROME ( 1 FDA reports)
HEPATOTOXICITY ( 1 FDA reports)
HISTOPLASMOSIS DISSEMINATED ( 1 FDA reports)
HIV TEST POSITIVE ( 1 FDA reports)
HYDRONEPHROSIS ( 1 FDA reports)
HYPERNATRAEMIA ( 1 FDA reports)
HYPOACUSIS ( 1 FDA reports)
HYPOPLASTIC LEFT HEART SYNDROME ( 1 FDA reports)
HYPOVOLAEMIA ( 1 FDA reports)
ILIAC ARTERY THROMBOSIS ( 1 FDA reports)
IMMUNE RECONSTITUTION SYNDROME ( 1 FDA reports)
IMPAIRED GASTRIC EMPTYING ( 1 FDA reports)
INCOHERENT ( 1 FDA reports)
INFLAMMATION ( 1 FDA reports)
INFUSION SITE PAIN ( 1 FDA reports)
INJECTION SITE HAEMORRHAGE ( 1 FDA reports)
INTERNATIONAL NORMALISED RATIO INCREASED ( 1 FDA reports)
INTRACARDIAC THROMBUS ( 1 FDA reports)
INTRACRANIAL PRESSURE INCREASED ( 1 FDA reports)
INTRAOCULAR PRESSURE DECREASED ( 1 FDA reports)
IRON DEFICIENCY ANAEMIA ( 1 FDA reports)
IRRITABILITY ( 1 FDA reports)
JAUNDICE ( 1 FDA reports)
JOINT RANGE OF MOTION DECREASED ( 1 FDA reports)
LABORATORY TEST INTERFERENCE ( 1 FDA reports)
LARGE INTESTINAL ULCER ( 1 FDA reports)
LARYNGEAL OEDEMA ( 1 FDA reports)
LASER THERAPY ( 1 FDA reports)
LEFT ATRIAL DILATATION ( 1 FDA reports)
LEUKAEMIA RECURRENT ( 1 FDA reports)
LEUKOCYTOSIS ( 1 FDA reports)
LIP DISORDER ( 1 FDA reports)
LIP EXFOLIATION ( 1 FDA reports)
LIP SWELLING ( 1 FDA reports)
LIPOMATOSIS ( 1 FDA reports)
LIVER ABSCESS ( 1 FDA reports)
LIVER INJURY ( 1 FDA reports)
LIVER TRANSPLANT REJECTION ( 1 FDA reports)
LUNG INFECTION PSEUDOMONAL ( 1 FDA reports)
MALIGNANT NEOPLASM PROGRESSION ( 1 FDA reports)
MASS ( 1 FDA reports)
MENINGITIS ( 1 FDA reports)
MENINGORRHAGIA ( 1 FDA reports)
MENTAL IMPAIRMENT ( 1 FDA reports)
METABOLIC DISORDER ( 1 FDA reports)
MUCOSAL HAEMORRHAGE ( 1 FDA reports)
MUSCULOSKELETAL PAIN ( 1 FDA reports)
NASAL FLARING ( 1 FDA reports)
NEPHROGENIC SYSTEMIC FIBROSIS ( 1 FDA reports)
NERVOUSNESS ( 1 FDA reports)
NOCARDIOSIS ( 1 FDA reports)
NORMOCHROMIC NORMOCYTIC ANAEMIA ( 1 FDA reports)
NUCLEAR MAGNETIC RESONANCE IMAGING BRAIN ABNORMAL ( 1 FDA reports)
OBLITERATIVE BRONCHIOLITIS ( 1 FDA reports)
OEDEMA ( 1 FDA reports)
OLIGURIA ( 1 FDA reports)
OPTIC ATROPHY ( 1 FDA reports)
ORAL DISORDER ( 1 FDA reports)
OSTEOMYELITIS ( 1 FDA reports)
OTOTOXICITY ( 1 FDA reports)
OVERDOSE ( 1 FDA reports)
OXYGEN SATURATION IMMEASURABLE ( 1 FDA reports)
PAIN ( 1 FDA reports)
PAPULE ( 1 FDA reports)
PARTIAL SEIZURES ( 1 FDA reports)
PERONEAL NERVE PALSY ( 1 FDA reports)
PHARYNGOLARYNGEAL PAIN ( 1 FDA reports)
PHOTOPHOBIA ( 1 FDA reports)
PITUITARY INFARCTION ( 1 FDA reports)
PLEURITIC PAIN ( 1 FDA reports)
PNEUMOCYSTIS JIROVECI PNEUMONIA ( 1 FDA reports)
PNEUMONIA ASPERGILLUS ( 1 FDA reports)
PNEUMONIA CRYPTOCOCCAL ( 1 FDA reports)
PNEUMONIA CYTOMEGALOVIRAL ( 1 FDA reports)
PNEUMONITIS ( 1 FDA reports)
PNEUMOPERITONEUM ( 1 FDA reports)
POOR PERIPHERAL CIRCULATION ( 1 FDA reports)
PORTAL HYPERTENSION ( 1 FDA reports)
PRODUCT QUALITY ISSUE ( 1 FDA reports)
PRURITUS ( 1 FDA reports)
PSEUDOMONAL SEPSIS ( 1 FDA reports)
PSEUDOMONAS TEST POSITIVE ( 1 FDA reports)
PULMONARY ALVEOLAR HAEMORRHAGE ( 1 FDA reports)
PULMONARY ARTERIAL PRESSURE INCREASED ( 1 FDA reports)
PULMONARY CAVITATION ( 1 FDA reports)
PULMONARY FIBROSIS ( 1 FDA reports)
PULMONARY FUNCTION TEST DECREASED ( 1 FDA reports)
PULMONARY GRANULOMA ( 1 FDA reports)
PULMONARY HAEMORRHAGE ( 1 FDA reports)
PULMONARY TOXICITY ( 1 FDA reports)
PUNCTURE SITE HAEMORRHAGE ( 1 FDA reports)
PUPILLARY REFLEX IMPAIRED ( 1 FDA reports)
PUPILS UNEQUAL ( 1 FDA reports)
PURULENCE ( 1 FDA reports)
PURULENT DISCHARGE ( 1 FDA reports)
QUADRIPARESIS ( 1 FDA reports)
RASH FOLLICULAR ( 1 FDA reports)
RASH GENERALISED ( 1 FDA reports)
RASH MACULAR ( 1 FDA reports)
REFUSAL OF TREATMENT BY RELATIVE ( 1 FDA reports)
RENAL DISORDER ( 1 FDA reports)
RESPIRATORY SYNCYTIAL VIRUS INFECTION ( 1 FDA reports)
RESPIRATORY TRACT INFECTION FUNGAL ( 1 FDA reports)
RESUSCITATION ( 1 FDA reports)
RETINAL OEDEMA ( 1 FDA reports)
RETINAL VASCULITIS ( 1 FDA reports)
RETROPERITONEAL NEOPLASM ( 1 FDA reports)
RHINITIS ( 1 FDA reports)
RIGHT ATRIAL DILATATION ( 1 FDA reports)
SCAB ( 1 FDA reports)
SCEDOSPORIUM INFECTION ( 1 FDA reports)
SCLERAL DISORDER ( 1 FDA reports)
SECRETION DISCHARGE ( 1 FDA reports)
SHOCK HAEMORRHAGIC ( 1 FDA reports)
SKIN DESQUAMATION ( 1 FDA reports)
SKIN HYPERPIGMENTATION ( 1 FDA reports)
SKIN HYPERTROPHY ( 1 FDA reports)
SKIN INDURATION ( 1 FDA reports)
SKIN INFECTION ( 1 FDA reports)
SKIN LESION ( 1 FDA reports)
SKIN REACTION ( 1 FDA reports)
SKIN ULCER ( 1 FDA reports)
SOPOR ( 1 FDA reports)
SPLENIC GRANULOMA ( 1 FDA reports)
SPLENIC INFARCTION ( 1 FDA reports)
SPLENIC LESION ( 1 FDA reports)
SPUTUM CULTURE POSITIVE ( 1 FDA reports)
SPUTUM DISCOLOURED ( 1 FDA reports)
STOMATITIS ( 1 FDA reports)
STREPTOCOCCAL BACTERAEMIA ( 1 FDA reports)
STUPOR ( 1 FDA reports)
SUBDURAL HAEMATOMA ( 1 FDA reports)
SUPRAVENTRICULAR EXTRASYSTOLES ( 1 FDA reports)
SUPRAVENTRICULAR TACHYCARDIA ( 1 FDA reports)
SYSTEMIC CANDIDA ( 1 FDA reports)
THERAPEUTIC RESPONSE UNEXPECTED ( 1 FDA reports)
TINNITUS ( 1 FDA reports)
TONGUE OEDEMA ( 1 FDA reports)
TONSILLAR DISORDER ( 1 FDA reports)
TOXICITY TO VARIOUS AGENTS ( 1 FDA reports)
TOXOPLASMOSIS ( 1 FDA reports)
TRACHEAL ULCER ( 1 FDA reports)
TRACHEOBRONCHITIS ( 1 FDA reports)
ULTRASOUND SCAN ABNORMAL ( 1 FDA reports)
UNRESPONSIVE TO STIMULI ( 1 FDA reports)
VAGINAL HAEMORRHAGE ( 1 FDA reports)
VARICES OESOPHAGEAL ( 1 FDA reports)
VASCULITIS ( 1 FDA reports)
VERTIGO ( 1 FDA reports)
VISUAL ACUITY REDUCED ( 1 FDA reports)
WEIGHT DECREASED ( 1 FDA reports)
WRONG DRUG ADMINISTERED ( 1 FDA reports)
ZYGOMYCOSIS ( 1 FDA reports)

© 2014 MedsFacts, Inc
Privacy Policy
Terms of Use