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HAEMORRHAGE INTRACRANIAL ( 79 FDA reports)
DIARRHOEA ( 53 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 43 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 43 FDA reports)
DEATH ( 40 FDA reports)
EXOMPHALOS ( 39 FDA reports)
CYTOLYTIC HEPATITIS ( 38 FDA reports)
BLADDER AGENESIS ( 35 FDA reports)
CLOACAL EXSTROPHY ( 34 FDA reports)
CAUDAL REGRESSION SYNDROME ( 33 FDA reports)
JAUNDICE ( 33 FDA reports)
MENINGOMYELOCELE ( 33 FDA reports)
LIPODYSTROPHY ACQUIRED ( 31 FDA reports)
BLOOD IRON DECREASED ( 30 FDA reports)
CEREBRAL HAEMORRHAGE ( 30 FDA reports)
CONVULSION ( 30 FDA reports)
LIVER FUNCTION TEST ABNORMAL ( 30 FDA reports)
MECONIUM STAIN ( 30 FDA reports)
UMBILICAL CORD ABNORMALITY ( 30 FDA reports)
CACHEXIA ( 29 FDA reports)
GASTROINTESTINAL DISORDER CONGENITAL ( 29 FDA reports)
GENITALIA EXTERNAL AMBIGUOUS ( 29 FDA reports)
CYTOMEGALOVIRUS INFECTION ( 26 FDA reports)
PYREXIA ( 25 FDA reports)
SEPSIS ( 25 FDA reports)
PORTAL HYPERTENSION ( 23 FDA reports)
RENAL FAILURE ACUTE ( 23 FDA reports)
CHOLESTASIS ( 22 FDA reports)
HEPATIC CIRRHOSIS ( 22 FDA reports)
HIV INFECTION ( 22 FDA reports)
HYPERTENSION ( 22 FDA reports)
MENINGITIS CRYPTOCOCCAL ( 22 FDA reports)
VARICES OESOPHAGEAL ( 21 FDA reports)
ANAL ATRESIA ( 20 FDA reports)
CONGENITAL GENITAL MALFORMATION ( 20 FDA reports)
CONGENITAL MUSCULOSKELETAL ANOMALY ( 20 FDA reports)
DRUG EXPOSURE DURING PREGNANCY ( 20 FDA reports)
CARDIAC FAILURE ( 19 FDA reports)
MALNUTRITION ( 19 FDA reports)
OVERDOSE ( 19 FDA reports)
PULMONARY EMBOLISM ( 19 FDA reports)
HEADACHE ( 18 FDA reports)
ASPERGILLOSIS ( 17 FDA reports)
GASTRITIS ( 17 FDA reports)
LACTIC ACIDOSIS ( 17 FDA reports)
PULMONARY OEDEMA ( 17 FDA reports)
RESPIRATORY TRACT INFECTION BACTERIAL ( 17 FDA reports)
BLOOD BILIRUBIN UNCONJUGATED INCREASED ( 16 FDA reports)
ANAEMIA ( 15 FDA reports)
ENCEPHALITIS VIRAL ( 15 FDA reports)
EPILEPSY ( 15 FDA reports)
ERYTHEMA ( 15 FDA reports)
HEPATITIS ( 15 FDA reports)
INTRACRANIAL HAEMATOMA ( 15 FDA reports)
LIVER TRANSPLANT ( 15 FDA reports)
BILIRUBIN CONJUGATED INCREASED ( 14 FDA reports)
CEREBROVASCULAR ACCIDENT ( 14 FDA reports)
DRUG INTERACTION ( 14 FDA reports)
GASTROINTESTINAL MALFORMATION ( 14 FDA reports)
HAEMARTHROSIS ( 14 FDA reports)
IMMUNE RECONSTITUTION SYNDROME ( 14 FDA reports)
NAUSEA ( 13 FDA reports)
TETHERED CORD SYNDROME ( 13 FDA reports)
TRANSAMINASES INCREASED ( 13 FDA reports)
ACQUIRED IMMUNODEFICIENCY SYNDROME ( 12 FDA reports)
FATIGUE ( 12 FDA reports)
HEPATIC ENZYME INCREASED ( 12 FDA reports)
PAIN IN EXTREMITY ( 12 FDA reports)
WEIGHT DECREASED ( 12 FDA reports)
DRUG INEFFECTIVE ( 11 FDA reports)
HAEMATOMA ( 11 FDA reports)
HEPATOTOXICITY ( 11 FDA reports)
LIVER DISORDER ( 11 FDA reports)
MENTAL STATUS CHANGES ( 11 FDA reports)
VOMITING ( 11 FDA reports)
ASTHENIA ( 10 FDA reports)
COUGH ( 10 FDA reports)
HEPATOCELLULAR INJURY ( 10 FDA reports)
INTRA-ABDOMINAL HAEMATOMA ( 10 FDA reports)
PREMATURE BABY ( 10 FDA reports)
BLOOD BILIRUBIN INCREASED ( 9 FDA reports)
CEREBRAL HAEMATOMA ( 9 FDA reports)
DEHYDRATION ( 9 FDA reports)
GAMMA-GLUTAMYLTRANSFERASE INCREASED ( 9 FDA reports)
MALAISE ( 9 FDA reports)
MUSCULOSKELETAL DEFORMITY ( 9 FDA reports)
ANOREXIA ( 8 FDA reports)
BLOOD ALKALINE PHOSPHATASE INCREASED ( 8 FDA reports)
FALL ( 8 FDA reports)
GASTROINTESTINAL DISORDER ( 8 FDA reports)
PREMATURE LABOUR ( 8 FDA reports)
RASH GENERALISED ( 8 FDA reports)
APHASIA ( 7 FDA reports)
ASCITES ( 7 FDA reports)
COMPLETED SUICIDE ( 7 FDA reports)
CONFUSIONAL STATE ( 7 FDA reports)
DISORIENTATION ( 7 FDA reports)
DYSPHAGIA ( 7 FDA reports)
EPISTAXIS ( 7 FDA reports)
HEPATIC FUNCTION ABNORMAL ( 7 FDA reports)
HEPATOCELLULAR DAMAGE ( 7 FDA reports)
HEPATOMEGALY ( 7 FDA reports)
KAPOSI'S SARCOMA ( 7 FDA reports)
RASH ( 7 FDA reports)
SKIN BURNING SENSATION ( 7 FDA reports)
STEVENS-JOHNSON SYNDROME ( 7 FDA reports)
VIRAL LOAD INCREASED ( 7 FDA reports)
AIDS DEMENTIA COMPLEX ( 6 FDA reports)
ARTHRALGIA ( 6 FDA reports)
BLOOD PRESSURE INCREASED ( 6 FDA reports)
BLOOD TRIGLYCERIDES INCREASED ( 6 FDA reports)
CEREBELLAR ATAXIA ( 6 FDA reports)
CEREBRAL INFARCTION ( 6 FDA reports)
CONGENITAL ANOMALY ( 6 FDA reports)
CORONARY ARTERY DISEASE ( 6 FDA reports)
DEMENTIA ( 6 FDA reports)
GRAND MAL CONVULSION ( 6 FDA reports)
HEART RATE INCREASED ( 6 FDA reports)
HYDROCEPHALUS ( 6 FDA reports)
INSOMNIA ( 6 FDA reports)
PRURITUS ( 6 FDA reports)
RASH MACULO-PAPULAR ( 6 FDA reports)
RENAL FAILURE ( 6 FDA reports)
SPINE MALFORMATION ( 6 FDA reports)
SUBCUTANEOUS ABSCESS ( 6 FDA reports)
SYNCOPE ( 6 FDA reports)
UPPER GASTROINTESTINAL HAEMORRHAGE ( 6 FDA reports)
ABDOMINAL HAEMATOMA ( 5 FDA reports)
ABDOMINAL PAIN UPPER ( 5 FDA reports)
ANGINA PECTORIS ( 5 FDA reports)
BRAIN OEDEMA ( 5 FDA reports)
CARDIAC FAILURE CONGESTIVE ( 5 FDA reports)
COAGULATION FACTOR DECREASED ( 5 FDA reports)
COMA HEPATIC ( 5 FDA reports)
CYTOMEGALOVIRUS OESOPHAGITIS ( 5 FDA reports)
DRUG HYPERSENSITIVITY ( 5 FDA reports)
EATON-LAMBERT SYNDROME ( 5 FDA reports)
GENERAL PHYSICAL HEALTH DETERIORATION ( 5 FDA reports)
HAEMORRHAGIC DIATHESIS ( 5 FDA reports)
HEPATIC FAILURE ( 5 FDA reports)
HEPATITIS B ( 5 FDA reports)
HYPERBILIRUBINAEMIA ( 5 FDA reports)
TREATMENT NONCOMPLIANCE ( 5 FDA reports)
ABORTION SPONTANEOUS ( 4 FDA reports)
AGITATION ( 4 FDA reports)
BICYTOPENIA ( 4 FDA reports)
BLOOD HIV RNA INCREASED ( 4 FDA reports)
BLOOD PRESSURE DECREASED ( 4 FDA reports)
BRAIN ABSCESS ( 4 FDA reports)
CAROTID ARTERY STENOSIS ( 4 FDA reports)
CHOLECYSTITIS ( 4 FDA reports)
COGNITIVE DISORDER ( 4 FDA reports)
DISEASE PROGRESSION ( 4 FDA reports)
DRUG SCREEN FALSE POSITIVE ( 4 FDA reports)
DYSAESTHESIA ( 4 FDA reports)
ENCEPHALITIS ( 4 FDA reports)
ENCEPHALOPATHY ( 4 FDA reports)
HAEMATOCHEZIA ( 4 FDA reports)
HAEMORRHAGE ( 4 FDA reports)
HEPATITIS CHOLESTATIC ( 4 FDA reports)
HYPERSENSITIVITY ( 4 FDA reports)
HYPERSOMNIA ( 4 FDA reports)
INJECTION SITE BRUISING ( 4 FDA reports)
INJECTION SITE HAEMATOMA ( 4 FDA reports)
LOWER LIMB FRACTURE ( 4 FDA reports)
METASTASES TO LUNG ( 4 FDA reports)
MYALGIA ( 4 FDA reports)
OEDEMA ( 4 FDA reports)
OESOPHAGEAL ADENOCARCINOMA ( 4 FDA reports)
OESOPHAGEAL CANDIDIASIS ( 4 FDA reports)
OSTEOMYELITIS ( 4 FDA reports)
PANCREATITIS ( 4 FDA reports)
REVERSIBLE ISCHAEMIC NEUROLOGICAL DEFICIT ( 4 FDA reports)
RHONCHI ( 4 FDA reports)
SPLENIC RUPTURE ( 4 FDA reports)
SPLENOMEGALY ( 4 FDA reports)
THROMBOCYTOPENIA ( 4 FDA reports)
URINE AMPHETAMINE POSITIVE ( 4 FDA reports)
BLOOD CREATININE INCREASED ( 3 FDA reports)
BLOOD PRESSURE SYSTOLIC INCREASED ( 3 FDA reports)
CANDIDIASIS ( 3 FDA reports)
CARDIAC ARREST ( 3 FDA reports)
CARDIAC TAMPONADE ( 3 FDA reports)
CARDIO-RESPIRATORY ARREST ( 3 FDA reports)
CHRONIC OBSTRUCTIVE PULMONARY DISEASE ( 3 FDA reports)
CUSHING'S SYNDROME ( 3 FDA reports)
DEPRESSION ( 3 FDA reports)
DIZZINESS ( 3 FDA reports)
EMBOLISM ( 3 FDA reports)
ESCHERICHIA BACTERAEMIA ( 3 FDA reports)
GASTROINTESTINAL HAEMORRHAGE ( 3 FDA reports)
HEAD INJURY ( 3 FDA reports)
HEPATIC STEATOSIS ( 3 FDA reports)
HEPATITIS C VIRUS ( 3 FDA reports)
HEPATOSPLENOMEGALY ( 3 FDA reports)
HYPOTHERMIA ( 3 FDA reports)
INFLAMMATION ( 3 FDA reports)
INJECTION SITE REACTION ( 3 FDA reports)
INTRAVENTRICULAR HAEMORRHAGE ( 3 FDA reports)
MICROLITHIASIS ( 3 FDA reports)
MUSCULOSKELETAL STIFFNESS ( 3 FDA reports)
NERVOUS SYSTEM DISORDER ( 3 FDA reports)
NEUTROPENIA ( 3 FDA reports)
NO THERAPEUTIC RESPONSE ( 3 FDA reports)
ORAL DISCOMFORT ( 3 FDA reports)
OSTEONECROSIS ( 3 FDA reports)
PANCREATITIS ACUTE ( 3 FDA reports)
PNEUMONIA ( 3 FDA reports)
POST PROCEDURAL HAEMORRHAGE ( 3 FDA reports)
PREGNANCY ( 3 FDA reports)
RENAL FAILURE CHRONIC ( 3 FDA reports)
RESPIRATORY ARREST ( 3 FDA reports)
RHABDOMYOLYSIS ( 3 FDA reports)
SOFT TISSUE HAEMORRHAGE ( 3 FDA reports)
STAPHYLOCOCCAL INFECTION ( 3 FDA reports)
STAPHYLOCOCCAL SEPSIS ( 3 FDA reports)
SUBCUTANEOUS NODULE ( 3 FDA reports)
ABASIA ( 2 FDA reports)
ACCIDENTAL DEATH ( 2 FDA reports)
ACUTE ABDOMEN ( 2 FDA reports)
ACUTE SINUSITIS ( 2 FDA reports)
ADVERSE DRUG REACTION ( 2 FDA reports)
ALANINE AMINOTRANSFERASE ABNORMAL ( 2 FDA reports)
ALOPECIA ( 2 FDA reports)
ANAEMIA OF CHRONIC DISEASE ( 2 FDA reports)
ANEURYSM ( 2 FDA reports)
ANTICONVULSANT DRUG LEVEL DECREASED ( 2 FDA reports)
ASPARTATE AMINOTRANSFERASE ABNORMAL ( 2 FDA reports)
ASPHYXIA ( 2 FDA reports)
ASTHMA ( 2 FDA reports)
BILIRUBIN CONJUGATED ABNORMAL ( 2 FDA reports)
BLOOD ALBUMIN DECREASED ( 2 FDA reports)
BLOOD OSMOLARITY DECREASED ( 2 FDA reports)
BONE DISORDER ( 2 FDA reports)
BRADYCARDIA ( 2 FDA reports)
CARDIAC DISORDER ( 2 FDA reports)
CD4 LYMPHOCYTES INCREASED ( 2 FDA reports)
COMPUTERISED TOMOGRAM ABNORMAL ( 2 FDA reports)
CONGENITAL APLASTIC ANAEMIA ( 2 FDA reports)
CRYPTOCOCCOSIS ( 2 FDA reports)
CULTURE URINE POSITIVE ( 2 FDA reports)
CYSTIC LYMPHANGIOMA ( 2 FDA reports)
CYTOMEGALOVIRUS CHORIORETINITIS ( 2 FDA reports)
DIET REFUSAL ( 2 FDA reports)
DISCOMFORT ( 2 FDA reports)
DRUG ABUSER ( 2 FDA reports)
DRUG INTOLERANCE ( 2 FDA reports)
DRUG LEVEL DECREASED ( 2 FDA reports)
DRUG RESISTANCE ( 2 FDA reports)
DRUG SCREEN POSITIVE ( 2 FDA reports)
ELECTROCARDIOGRAM PR PROLONGATION ( 2 FDA reports)
EOSINOPHILIA ( 2 FDA reports)
EYELID DISORDER ( 2 FDA reports)
EYELID PTOSIS ( 2 FDA reports)
GASTRITIS HAEMORRHAGIC ( 2 FDA reports)
GENERAL PHYSICAL CONDITION ABNORMAL ( 2 FDA reports)
GINGIVAL BLEEDING ( 2 FDA reports)
GLOMERULAR FILTRATION RATE DECREASED ( 2 FDA reports)
HAEMODIALYSIS ( 2 FDA reports)
HAEMODYNAMIC INSTABILITY ( 2 FDA reports)
HAEMOLYTIC URAEMIC SYNDROME ( 2 FDA reports)
HAEMOPTYSIS ( 2 FDA reports)
HALLUCINATION, AUDITORY ( 2 FDA reports)
HEPATIC FIBROSIS ( 2 FDA reports)
HEPATIC HAEMORRHAGE ( 2 FDA reports)
HEPATITIS C ( 2 FDA reports)
HEPATITIS C POSITIVE ( 2 FDA reports)
HEPATITIS C VIRUS TEST ( 2 FDA reports)
HERPES VIRUS INFECTION ( 2 FDA reports)
HERPES ZOSTER ( 2 FDA reports)
HYPERCHOLESTEROLAEMIA ( 2 FDA reports)
INJECTION SITE PAIN ( 2 FDA reports)
INTESTINAL PERFORATION ( 2 FDA reports)
KAPOSI'S SARCOMA AIDS RELATED ( 2 FDA reports)
LARYNGEAL CANCER ( 2 FDA reports)
LIP SWELLING ( 2 FDA reports)
LOSS OF CONSCIOUSNESS ( 2 FDA reports)
LUNG INFILTRATION ( 2 FDA reports)
LUNG NEOPLASM MALIGNANT ( 2 FDA reports)
LYMPHADENOPATHY ( 2 FDA reports)
LYMPHOMA ( 2 FDA reports)
MELAENA ( 2 FDA reports)
MONOPARESIS ( 2 FDA reports)
MUCOSAL HAEMORRHAGE ( 2 FDA reports)
MUSCLE DISORDER ( 2 FDA reports)
MUSCLE HAEMORRHAGE ( 2 FDA reports)
MYCOTIC ANEURYSM ( 2 FDA reports)
NEONATAL ASPIRATION ( 2 FDA reports)
NEUROLOGICAL SYMPTOM ( 2 FDA reports)
NEUROPATHY PERIPHERAL ( 2 FDA reports)
OSTEOARTHRITIS ( 2 FDA reports)
PAIN ( 2 FDA reports)
PANCREATIC ENZYMES INCREASED ( 2 FDA reports)
PARESIS ( 2 FDA reports)
PHARYNGITIS ( 2 FDA reports)
PHOTOSENSITIVITY REACTION ( 2 FDA reports)
PLATELET COUNT DECREASED ( 2 FDA reports)
PROTHROMBIN LEVEL DECREASED ( 2 FDA reports)
PSYCHOMOTOR HYPERACTIVITY ( 2 FDA reports)
PURPURA ( 2 FDA reports)
RASH PAPULAR ( 2 FDA reports)
RASH PRURITIC ( 2 FDA reports)
RESPIRATORY FAILURE ( 2 FDA reports)
RETINAL DEGENERATION ( 2 FDA reports)
SIMPLE PARTIAL SEIZURES ( 2 FDA reports)
SINUSITIS ( 2 FDA reports)
SKIN TOXICITY ( 2 FDA reports)
SUBARACHNOID HAEMORRHAGE ( 2 FDA reports)
SUDDEN DEATH ( 2 FDA reports)
SUICIDAL IDEATION ( 2 FDA reports)
SUNBURN ( 2 FDA reports)
THROMBOCYTOPENIC PURPURA ( 2 FDA reports)
TINNITUS ( 2 FDA reports)
TOXOPLASMOSIS ( 2 FDA reports)
VIRAL LOAD DECREASED ( 2 FDA reports)
WHEELCHAIR USER ( 2 FDA reports)
ABDOMINAL DISTENSION ( 1 FDA reports)
ABDOMINAL PAIN ( 1 FDA reports)
ACCIDENT ( 1 FDA reports)
ACTIVATED PARTIAL THROMBOPLASTIN TIME PROLONGED ( 1 FDA reports)
ACUTE HEPATIC FAILURE ( 1 FDA reports)
ACUTE MYOCARDIAL INFARCTION ( 1 FDA reports)
ACUTE PRERENAL FAILURE ( 1 FDA reports)
AGRANULOCYTOSIS ( 1 FDA reports)
AIDS ENCEPHALOPATHY ( 1 FDA reports)
ALKALOSIS ( 1 FDA reports)
ALTERED STATE OF CONSCIOUSNESS ( 1 FDA reports)
APPENDICITIS PERFORATED ( 1 FDA reports)
ATAXIA ( 1 FDA reports)
ATRIAL FIBRILLATION ( 1 FDA reports)
AUTOIMMUNE HEPATITIS ( 1 FDA reports)
BACTERAEMIA ( 1 FDA reports)
BLINDNESS ( 1 FDA reports)
BLINDNESS CORTICAL ( 1 FDA reports)
BLINDNESS UNILATERAL ( 1 FDA reports)
BLOOD AMYLASE INCREASED ( 1 FDA reports)
BLOOD CHOLESTEROL INCREASED ( 1 FDA reports)
BLOOD CREATINE PHOSPHOKINASE INCREASED ( 1 FDA reports)
BRONCHITIS ( 1 FDA reports)
CAESAREAN SECTION ( 1 FDA reports)
CALCINOSIS ( 1 FDA reports)
CATHETER RELATED INFECTION ( 1 FDA reports)
CD4 LYMPHOCYTES DECREASED ( 1 FDA reports)
CENTRAL NERVOUS SYSTEM INFLAMMATION ( 1 FDA reports)
CENTRAL NERVOUS SYSTEM LYMPHOMA ( 1 FDA reports)
CERVICAL SPINAL STENOSIS ( 1 FDA reports)
CHEILITIS ( 1 FDA reports)
CHRONIC HEPATITIS ( 1 FDA reports)
COLORECTAL CANCER ( 1 FDA reports)
CONDITION AGGRAVATED ( 1 FDA reports)
CONGENITAL SPINAL CORD ANOMALY ( 1 FDA reports)
CONSTIPATION ( 1 FDA reports)
CYTOMEGALOVIRUS COLITIS ( 1 FDA reports)
CYTOMEGALOVIRUS TEST ( 1 FDA reports)
DEAFNESS ( 1 FDA reports)
DEPRESSED LEVEL OF CONSCIOUSNESS ( 1 FDA reports)
DERMATITIS ALLERGIC ( 1 FDA reports)
DIABETES MELLITUS ( 1 FDA reports)
DIALYSIS ( 1 FDA reports)
DRUG ADMINISTRATION ERROR ( 1 FDA reports)
DRUG EFFECT DECREASED ( 1 FDA reports)
DRUG EXPOSURE BEFORE PREGNANCY ( 1 FDA reports)
DRUG TOXICITY ( 1 FDA reports)
DRY MOUTH ( 1 FDA reports)
DYSARTHRIA ( 1 FDA reports)
DYSPNOEA ( 1 FDA reports)
DYSPNOEA EXERTIONAL ( 1 FDA reports)
EJECTION FRACTION ABNORMAL ( 1 FDA reports)
END STAGE AIDS ( 1 FDA reports)
ENDOSCOPY GASTROINTESTINAL ( 1 FDA reports)
ENTEROBACTER INFECTION ( 1 FDA reports)
ENTEROCOCCAL INFECTION ( 1 FDA reports)
FACIAL PALSY ( 1 FDA reports)
FEELING OF BODY TEMPERATURE CHANGE ( 1 FDA reports)
FOLLICULITIS ( 1 FDA reports)
GAIT DISTURBANCE ( 1 FDA reports)
GALLBLADDER DISORDER ( 1 FDA reports)
GASTRIC DISORDER ( 1 FDA reports)
GASTROENTERITIS ( 1 FDA reports)
GASTROENTERITIS CRYPTOSPORIDIAL ( 1 FDA reports)
GASTROOESOPHAGEAL REFLUX DISEASE ( 1 FDA reports)
HAEMANGIOMA OF LIVER ( 1 FDA reports)
HAEMOLYTIC ANAEMIA ( 1 FDA reports)
HAEMORRHOIDAL HAEMORRHAGE ( 1 FDA reports)
HELICOBACTER PYLORI IDENTIFICATION TEST POSITIVE ( 1 FDA reports)
HEPATIC ENZYME ABNORMAL ( 1 FDA reports)
HEPATIC PAIN ( 1 FDA reports)
HERNIA OBSTRUCTIVE ( 1 FDA reports)
HIV WASTING SYNDROME ( 1 FDA reports)
HODGKIN'S DISEASE ( 1 FDA reports)
HYPERHIDROSIS ( 1 FDA reports)
HYPERTRIGLYCERIDAEMIA ( 1 FDA reports)
HYPOCHOLESTEROLAEMIA ( 1 FDA reports)
HYPONATRAEMIA ( 1 FDA reports)
HYPOPHAGIA ( 1 FDA reports)
HYPOTENSION ( 1 FDA reports)
ILEUS ( 1 FDA reports)
ILL-DEFINED DISORDER ( 1 FDA reports)
INFARCTION ( 1 FDA reports)
INJECTION SITE ABSCESS ( 1 FDA reports)
INJECTION SITE NECROSIS ( 1 FDA reports)
INTERNATIONAL NORMALISED RATIO INCREASED ( 1 FDA reports)
JAW FRACTURE ( 1 FDA reports)
JOINT SWELLING ( 1 FDA reports)
LIVER SCAN ABNORMAL ( 1 FDA reports)
LUNG NEOPLASM ( 1 FDA reports)
LYMPHOCYTE COUNT INCREASED ( 1 FDA reports)
MALLORY-WEISS SYNDROME ( 1 FDA reports)
MATERNAL DRUGS AFFECTING FOETUS ( 1 FDA reports)
MECONIUM IN AMNIOTIC FLUID ( 1 FDA reports)
MEDICATION ERROR ( 1 FDA reports)
MEMORY IMPAIRMENT ( 1 FDA reports)
MENINGITIS ASEPTIC ( 1 FDA reports)
MENINGITIS BACTERIAL ( 1 FDA reports)
MULTI-ORGAN FAILURE ( 1 FDA reports)
MULTIPLE-DRUG RESISTANCE ( 1 FDA reports)
MUSCLE SPASMS ( 1 FDA reports)
MYCOBACTERIAL INFECTION ( 1 FDA reports)
NASOPHARYNGITIS ( 1 FDA reports)
NECROTISING RETINITIS ( 1 FDA reports)
NEURALGIA ( 1 FDA reports)
NIGHTMARE ( 1 FDA reports)
NON-HODGKIN'S LYMPHOMA ( 1 FDA reports)
OESOPHAGEAL INFECTION ( 1 FDA reports)
OESOPHAGITIS ( 1 FDA reports)
ORCHITIS ( 1 FDA reports)
PALLOR ( 1 FDA reports)
PARANEOPLASTIC SYNDROME ( 1 FDA reports)
PARKINSONISM ( 1 FDA reports)
PATHOGEN RESISTANCE ( 1 FDA reports)
PERICARDIAL HAEMORRHAGE ( 1 FDA reports)
PNEUMOCYSTIS JIROVECI PNEUMONIA ( 1 FDA reports)
PROGRESSIVE MULTIFOCAL LEUKOENCEPHALOPATHY ( 1 FDA reports)
PROSTATITIS ( 1 FDA reports)
PROTEUS INFECTION ( 1 FDA reports)
PULMONARY ARTERY THROMBOSIS ( 1 FDA reports)
PULMONARY HYPERTENSION ( 1 FDA reports)
RASH MACULAR ( 1 FDA reports)
RECTAL ABSCESS ( 1 FDA reports)
RECTAL HAEMORRHAGE ( 1 FDA reports)
RENAL DISORDER ( 1 FDA reports)
RENAL IMPAIRMENT ( 1 FDA reports)
RENAL TUBULAR NECROSIS ( 1 FDA reports)
RESPIRATORY DISTRESS ( 1 FDA reports)
RETINAL HAEMORRHAGE ( 1 FDA reports)
RETROVIRAL REBOUND SYNDROME ( 1 FDA reports)
RHINITIS ( 1 FDA reports)
ROAD TRAFFIC ACCIDENT ( 1 FDA reports)
SEPSIS NEONATAL ( 1 FDA reports)
SEPTIC EMBOLUS ( 1 FDA reports)
SEPTIC SHOCK ( 1 FDA reports)
SKIN HAEMORRHAGE ( 1 FDA reports)
SKIN HYPERTROPHY ( 1 FDA reports)
SLEEP DISORDER ( 1 FDA reports)
SOMNOLENCE ( 1 FDA reports)
SPEECH DISORDER ( 1 FDA reports)
SPLENIC HAEMORRHAGE ( 1 FDA reports)
SPUTUM DISCOLOURED ( 1 FDA reports)
STAPHYLOCOCCAL BACTERAEMIA ( 1 FDA reports)
STOMATITIS ( 1 FDA reports)
SUICIDE ATTEMPT ( 1 FDA reports)
SUPRAVENTRICULAR TACHYCARDIA ( 1 FDA reports)
SWELLING ( 1 FDA reports)
THERAPY NON-RESPONDER ( 1 FDA reports)
TUBULOINTERSTITIAL NEPHRITIS ( 1 FDA reports)
TYPE 2 DIABETES MELLITUS ( 1 FDA reports)
URETHRITIS ( 1 FDA reports)
URINARY RETENTION ( 1 FDA reports)
URINARY TRACT INFECTION ( 1 FDA reports)
VIRAL INFECTION ( 1 FDA reports)
VISUAL FIELD DEFECT ( 1 FDA reports)
VOCAL CORD DISORDER ( 1 FDA reports)
WALKING AID USER ( 1 FDA reports)
WHEEZING ( 1 FDA reports)
WHITE BLOOD CELL COUNT DECREASED ( 1 FDA reports)
WOUND INFECTION ( 1 FDA reports)

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