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

NAUSEA ( 77 FDA reports)
HYPERLIPIDAEMIA ( 75 FDA reports)
LIPODYSTROPHY ACQUIRED ( 67 FDA reports)
PYREXIA ( 63 FDA reports)
DIZZINESS ( 61 FDA reports)
GAMMA-GLUTAMYLTRANSFERASE INCREASED ( 60 FDA reports)
VOMITING ( 59 FDA reports)
HEPATIC FUNCTION ABNORMAL ( 57 FDA reports)
BLOOD ALKALINE PHOSPHATASE INCREASED ( 52 FDA reports)
DIARRHOEA ( 52 FDA reports)
MITOCHONDRIAL TOXICITY ( 46 FDA reports)
RASH ( 43 FDA reports)
DIPLOPIA ( 42 FDA reports)
EYELID PTOSIS ( 42 FDA reports)
IMMUNE RECONSTITUTION SYNDROME ( 40 FDA reports)
DEATH ( 39 FDA reports)
PROGRESSIVE EXTERNAL OPHTHALMOPLEGIA ( 39 FDA reports)
RENAL IMPAIRMENT ( 36 FDA reports)
PALPITATIONS ( 35 FDA reports)
ANAEMIA ( 32 FDA reports)
WEIGHT DECREASED ( 32 FDA reports)
BLOOD TRIGLYCERIDES INCREASED ( 30 FDA reports)
DIABETES MELLITUS ( 30 FDA reports)
NERVOUS SYSTEM DISORDER ( 30 FDA reports)
INFLUENZA LIKE ILLNESS ( 29 FDA reports)
CALCULUS URINARY ( 27 FDA reports)
RENAL FAILURE ACUTE ( 27 FDA reports)
PULMONARY HYPERTENSION ( 26 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 25 FDA reports)
HEADACHE ( 25 FDA reports)
TREMOR ( 25 FDA reports)
LYMPHADENOPATHY ( 24 FDA reports)
FIBRIN DEGRADATION PRODUCTS INCREASED ( 23 FDA reports)
CACHEXIA ( 22 FDA reports)
MALAISE ( 22 FDA reports)
RENAL FAILURE ( 22 FDA reports)
JAUNDICE ( 21 FDA reports)
PAIN ( 21 FDA reports)
CREATININE RENAL CLEARANCE DECREASED ( 20 FDA reports)
DRUG TOXICITY ( 20 FDA reports)
LYMPHOMA ( 20 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 19 FDA reports)
BLOOD CHOLESTEROL INCREASED ( 19 FDA reports)
FATIGUE ( 19 FDA reports)
PNEUMONIA ( 19 FDA reports)
HEPATIC STEATOSIS ( 18 FDA reports)
HYPERTENSION ( 18 FDA reports)
LIVER DISORDER ( 18 FDA reports)
SUBDURAL HAEMATOMA ( 18 FDA reports)
ABDOMINAL PAIN UPPER ( 17 FDA reports)
BRADYCARDIA ( 17 FDA reports)
DRUG EXPOSURE DURING PREGNANCY ( 17 FDA reports)
DRUG INTERACTION ( 17 FDA reports)
MYALGIA ( 17 FDA reports)
NEUROPATHY PERIPHERAL ( 17 FDA reports)
DRUG HYPERSENSITIVITY ( 16 FDA reports)
DRUG INEFFECTIVE ( 16 FDA reports)
HIV WASTING SYNDROME ( 16 FDA reports)
PRURITUS ( 16 FDA reports)
OEDEMA PERIPHERAL ( 15 FDA reports)
ABDOMINAL PAIN ( 14 FDA reports)
ASTHENIA ( 14 FDA reports)
CONVULSION ( 14 FDA reports)
MYOPATHY ( 14 FDA reports)
VISUAL DISTURBANCE ( 14 FDA reports)
ARTHRALGIA ( 13 FDA reports)
DRUG RESISTANCE ( 13 FDA reports)
MYOCARDIAL INFARCTION ( 13 FDA reports)
ORAL CANDIDIASIS ( 13 FDA reports)
BACK PAIN ( 12 FDA reports)
BLOOD BILIRUBIN INCREASED ( 12 FDA reports)
BLOOD LACTIC ACID INCREASED ( 12 FDA reports)
DYSPNOEA ( 12 FDA reports)
GENERAL PHYSICAL HEALTH DETERIORATION ( 12 FDA reports)
HEPATITIS ( 12 FDA reports)
MUSCULAR WEAKNESS ( 12 FDA reports)
PARKINSONISM ( 12 FDA reports)
VISUAL IMPAIRMENT ( 12 FDA reports)
ACUTE HEPATIC FAILURE ( 11 FDA reports)
CARDIOMEGALY ( 11 FDA reports)
CEREBRAL INFARCTION ( 11 FDA reports)
DEHYDRATION ( 11 FDA reports)
DYSLIPIDAEMIA ( 11 FDA reports)
ELECTROLYTE IMBALANCE ( 11 FDA reports)
HEPATOMEGALY ( 11 FDA reports)
HYPOAESTHESIA ( 11 FDA reports)
OESOPHAGEAL CANDIDIASIS ( 11 FDA reports)
PREGNANCY ( 11 FDA reports)
RENAL TUBULAR NECROSIS ( 11 FDA reports)
SOMNOLENCE ( 11 FDA reports)
TACHYCARDIA ( 11 FDA reports)
BRAIN HERNIATION ( 10 FDA reports)
CHILLS ( 10 FDA reports)
COUGH ( 10 FDA reports)
DECREASED APPETITE ( 10 FDA reports)
EXTRASYSTOLES ( 10 FDA reports)
GRAFT DYSFUNCTION ( 10 FDA reports)
HAEMARTHROSIS ( 10 FDA reports)
HEPATIC CIRRHOSIS ( 10 FDA reports)
HEPATIC ENCEPHALOPATHY ( 10 FDA reports)
INSOMNIA ( 10 FDA reports)
LIPOATROPHY ( 10 FDA reports)
NEPHROTIC SYNDROME ( 10 FDA reports)
OSTEONECROSIS ( 10 FDA reports)
PHARYNGITIS ( 10 FDA reports)
PNEUMOCYSTIS JIROVECI PNEUMONIA ( 10 FDA reports)
RASH MACULO-PAPULAR ( 10 FDA reports)
TRANSPLANT REJECTION ( 10 FDA reports)
VENTRICULAR EXTRASYSTOLES ( 10 FDA reports)
ANOREXIA ( 9 FDA reports)
ARRHYTHMIA ( 9 FDA reports)
BLOOD ELECTROLYTES ABNORMAL ( 9 FDA reports)
CONDITION AGGRAVATED ( 9 FDA reports)
DEPRESSION ( 9 FDA reports)
DISTURBANCE IN ATTENTION ( 9 FDA reports)
EYE DISORDER ( 9 FDA reports)
HAEMOGLOBIN DECREASED ( 9 FDA reports)
HEPATIC NECROSIS ( 9 FDA reports)
HYPERCHOLESTEROLAEMIA ( 9 FDA reports)
HYPERSENSITIVITY ( 9 FDA reports)
HYPERTRIGLYCERIDAEMIA ( 9 FDA reports)
IMMUNOSUPPRESSANT DRUG LEVEL INCREASED ( 9 FDA reports)
RHABDOMYOLYSIS ( 9 FDA reports)
SUBARACHNOID HAEMORRHAGE ( 9 FDA reports)
CHOLESTASIS ( 8 FDA reports)
DISEASE RECURRENCE ( 8 FDA reports)
HYPERHIDROSIS ( 8 FDA reports)
HYPERLACTACIDAEMIA ( 8 FDA reports)
HYPOKALAEMIA ( 8 FDA reports)
LIVER FUNCTION TEST ABNORMAL ( 8 FDA reports)
LIVER TRANSPLANT ( 8 FDA reports)
MASS ( 8 FDA reports)
MEMORY IMPAIRMENT ( 8 FDA reports)
NEUTROPENIA ( 8 FDA reports)
PULMONARY EMBOLISM ( 8 FDA reports)
RESPIRATORY FAILURE ( 8 FDA reports)
STAPHYLOCOCCAL SEPSIS ( 8 FDA reports)
WEIGHT INCREASED ( 8 FDA reports)
ABDOMINAL DISCOMFORT ( 7 FDA reports)
ASCITES ( 7 FDA reports)
BLOOD AMYLASE INCREASED ( 7 FDA reports)
BLOOD SODIUM DECREASED ( 7 FDA reports)
CARDIAC TAMPONADE ( 7 FDA reports)
CEREBRAL TOXOPLASMOSIS ( 7 FDA reports)
CHOLELITHIASIS ( 7 FDA reports)
ERYTHEMA ( 7 FDA reports)
FALL ( 7 FDA reports)
FAT REDISTRIBUTION ( 7 FDA reports)
HEPATIC ENZYME INCREASED ( 7 FDA reports)
IMPETIGO ( 7 FDA reports)
INTRA-UTERINE DEATH ( 7 FDA reports)
LACTIC ACIDOSIS ( 7 FDA reports)
LIP EROSION ( 7 FDA reports)
MUSCLE HAEMORRHAGE ( 7 FDA reports)
PANCYTOPENIA ( 7 FDA reports)
PLATELET COUNT DECREASED ( 7 FDA reports)
PRODUCTIVE COUGH ( 7 FDA reports)
SMALL FOR DATES BABY ( 7 FDA reports)
STAPHYLOCOCCAL INFECTION ( 7 FDA reports)
THROMBOCYTOPENIA ( 7 FDA reports)
WHITE BLOOD CELL COUNT DECREASED ( 7 FDA reports)
ACUTE PSYCHOSIS ( 6 FDA reports)
BLOOD IMMUNOGLOBULIN E INCREASED ( 6 FDA reports)
BLOOD LACTATE DEHYDROGENASE INCREASED ( 6 FDA reports)
CHEST PAIN ( 6 FDA reports)
CHOLECYSTITIS ACUTE ( 6 FDA reports)
CUSHING'S SYNDROME ( 6 FDA reports)
DUODENAL ULCER ( 6 FDA reports)
DYSPHAGIA ( 6 FDA reports)
FACIAL WASTING ( 6 FDA reports)
GASTROINTESTINAL DISORDER ( 6 FDA reports)
GUILLAIN-BARRE SYNDROME ( 6 FDA reports)
HAEMATURIA ( 6 FDA reports)
HAEMOLYTIC ANAEMIA ( 6 FDA reports)
HYPERBILIRUBINAEMIA ( 6 FDA reports)
KAPOSI'S SARCOMA ( 6 FDA reports)
LEUKOPENIA ( 6 FDA reports)
LIPOHYPERTROPHY ( 6 FDA reports)
METABOLIC DISORDER ( 6 FDA reports)
MULTI-ORGAN DISORDER ( 6 FDA reports)
OPHTHALMOPLEGIA ( 6 FDA reports)
PROTEINURIA ( 6 FDA reports)
PULMONARY TUBERCULOSIS ( 6 FDA reports)
RETINAL VEIN OCCLUSION ( 6 FDA reports)
URINE COLOUR ABNORMAL ( 6 FDA reports)
ABDOMINAL DISTENSION ( 5 FDA reports)
ABORTION SPONTANEOUS ( 5 FDA reports)
ABSCESS ( 5 FDA reports)
BLOOD CHLORIDE DECREASED ( 5 FDA reports)
BLOOD PHOSPHORUS DECREASED ( 5 FDA reports)
BLOOD PRESSURE INCREASED ( 5 FDA reports)
C-REACTIVE PROTEIN INCREASED ( 5 FDA reports)
CARDIAC FAILURE ( 5 FDA reports)
CD4 LYMPHOCYTES DECREASED ( 5 FDA reports)
CHOLECYSTECTOMY ( 5 FDA reports)
CYTOLYTIC HEPATITIS ( 5 FDA reports)
CYTOMEGALOVIRUS CHORIORETINITIS ( 5 FDA reports)
DEPRESSED LEVEL OF CONSCIOUSNESS ( 5 FDA reports)
DIALYSIS ( 5 FDA reports)
DRUG ERUPTION ( 5 FDA reports)
DRUG LEVEL DECREASED ( 5 FDA reports)
ELECTROCARDIOGRAM QT PROLONGED ( 5 FDA reports)
HAEMORRHAGE ( 5 FDA reports)
HEPATIC FAILURE ( 5 FDA reports)
HEPATOCELLULAR DAMAGE ( 5 FDA reports)
HEPATOTOXICITY ( 5 FDA reports)
INFLUENZA ( 5 FDA reports)
INTRAVASCULAR HAEMOLYSIS ( 5 FDA reports)
IRRITABILITY ( 5 FDA reports)
LIVER TRANSPLANT REJECTION ( 5 FDA reports)
LOSS OF CONSCIOUSNESS ( 5 FDA reports)
MENTAL STATUS CHANGES ( 5 FDA reports)
MUSCLE SPASMS ( 5 FDA reports)
MYCOBACTERIUM AVIUM COMPLEX INFECTION ( 5 FDA reports)
NODULAR REGENERATIVE HYPERPLASIA ( 5 FDA reports)
PAIN IN EXTREMITY ( 5 FDA reports)
PANCREATITIS ( 5 FDA reports)
PARAESTHESIA ( 5 FDA reports)
PNEUMOCYSTIS CARINII PNEUMONIA ( 5 FDA reports)
PROGRESSIVE MULTIFOCAL LEUKOENCEPHALOPATHY ( 5 FDA reports)
RASH ERYTHEMATOUS ( 5 FDA reports)
SLEEP DISORDER ( 5 FDA reports)
SUPRAVENTRICULAR EXTRASYSTOLES ( 5 FDA reports)
TRANSFUSION REACTION ( 5 FDA reports)
VENTRICULAR ARRHYTHMIA ( 5 FDA reports)
AIDS ENCEPHALOPATHY ( 4 FDA reports)
ANOGENITAL WARTS ( 4 FDA reports)
BLOOD URIC ACID INCREASED ( 4 FDA reports)
BODY TEMPERATURE INCREASED ( 4 FDA reports)
BRAIN MASS ( 4 FDA reports)
CARDIAC ARREST ( 4 FDA reports)
CEREBRAL HAEMORRHAGE ( 4 FDA reports)
CHEST DISCOMFORT ( 4 FDA reports)
CLOSTRIDIUM COLITIS ( 4 FDA reports)
COLON OPERATION ( 4 FDA reports)
CONSTIPATION ( 4 FDA reports)
DIFFICULTY IN WALKING ( 4 FDA reports)
GASTROOESOPHAGEAL REFLUX DISEASE ( 4 FDA reports)
GLIOMA ( 4 FDA reports)
HAEMATOCRIT DECREASED ( 4 FDA reports)
HEPATIC FIBROSIS ( 4 FDA reports)
HEPATITIS B ( 4 FDA reports)
HERPES ZOSTER ( 4 FDA reports)
HIV INFECTION ( 4 FDA reports)
HYPERAMYLASAEMIA ( 4 FDA reports)
INCREASED APPETITE ( 4 FDA reports)
LIPIDS INCREASED ( 4 FDA reports)
LIVER INJURY ( 4 FDA reports)
LOBAR PNEUMONIA ( 4 FDA reports)
LOW DENSITY LIPOPROTEIN INCREASED ( 4 FDA reports)
LYMPHADENITIS ( 4 FDA reports)
MYOCARDIAL ISCHAEMIA ( 4 FDA reports)
NEPHRITIS INTERSTITIAL ( 4 FDA reports)
NEUROGENIC BLADDER ( 4 FDA reports)
NO THERAPEUTIC RESPONSE ( 4 FDA reports)
PANCREATITIS ACUTE ( 4 FDA reports)
PRE-ECLAMPSIA ( 4 FDA reports)
PSYCHIATRIC SYMPTOM ( 4 FDA reports)
PURULENCE ( 4 FDA reports)
RASH PRURITIC ( 4 FDA reports)
SEPTIC SHOCK ( 4 FDA reports)
SICK SINUS SYNDROME ( 4 FDA reports)
SLEEP APNOEA SYNDROME ( 4 FDA reports)
SPLENOMEGALY ( 4 FDA reports)
ABDOMINAL TENDERNESS ( 3 FDA reports)
ADENOVIRUS INFECTION ( 3 FDA reports)
AGRANULOCYTOSIS ( 3 FDA reports)
ANURIA ( 3 FDA reports)
ANXIETY ( 3 FDA reports)
APHASIA ( 3 FDA reports)
APLASIA CUTIS CONGENITA ( 3 FDA reports)
BALANCE DISORDER ( 3 FDA reports)
BLINDNESS ( 3 FDA reports)
BLOOD CORTISOL DECREASED ( 3 FDA reports)
BLOOD CREATININE INCREASED ( 3 FDA reports)
BRONCHOPULMONARY ASPERGILLOSIS ( 3 FDA reports)
CAESAREAN SECTION ( 3 FDA reports)
CEREBROVASCULAR ACCIDENT ( 3 FDA reports)
COGNITIVE DISORDER ( 3 FDA reports)
CONFUSIONAL STATE ( 3 FDA reports)
CORONARY ARTERY OCCLUSION ( 3 FDA reports)
CORTISOL FREE URINE DECREASED ( 3 FDA reports)
CYTOMEGALOVIRUS INFECTION ( 3 FDA reports)
CYTOMEGALOVIRUS OESOPHAGITIS ( 3 FDA reports)
DERMATITIS ALLERGIC ( 3 FDA reports)
DERMATITIS EXFOLIATIVE ( 3 FDA reports)
DRUG INTOLERANCE ( 3 FDA reports)
DYSARTHRIA ( 3 FDA reports)
ENCEPHALITIS ( 3 FDA reports)
ENCEPHALOPATHY ( 3 FDA reports)
ENTEROCOLITIS ( 3 FDA reports)
EOSINOPHILIA ( 3 FDA reports)
EPILEPSY ( 3 FDA reports)
FEELING ABNORMAL ( 3 FDA reports)
GASTROENTERITIS ( 3 FDA reports)
GYNAECOMASTIA ( 3 FDA reports)
HAEMATOMA ( 3 FDA reports)
HAPTOGLOBIN DECREASED ( 3 FDA reports)
HEMIPARESIS ( 3 FDA reports)
HEPATITIS FULMINANT ( 3 FDA reports)
HIGH DENSITY LIPOPROTEIN DECREASED ( 3 FDA reports)
HYPERPHAGIA ( 3 FDA reports)
HYPOALBUMINAEMIA ( 3 FDA reports)
HYPONATRAEMIA ( 3 FDA reports)
ILL-DEFINED DISORDER ( 3 FDA reports)
INTENTIONAL MISUSE ( 3 FDA reports)
IRON DEFICIENCY ( 3 FDA reports)
KLEBSIELLA SEPSIS ( 3 FDA reports)
LEUKOCYTOSIS ( 3 FDA reports)
LIPIDS ABNORMAL ( 3 FDA reports)
LOCALISED OSTEOARTHRITIS ( 3 FDA reports)
MATERNAL DRUGS AFFECTING FOETUS ( 3 FDA reports)
MEASLES ( 3 FDA reports)
METABOLIC ACIDOSIS ( 3 FDA reports)
MOBILITY DECREASED ( 3 FDA reports)
MYELODYSPLASTIC SYNDROME ( 3 FDA reports)
NEPHROLITHIASIS ( 3 FDA reports)
OCULAR ICTERUS ( 3 FDA reports)
OEDEMA ( 3 FDA reports)
OLIGURIA ( 3 FDA reports)
PATHOGEN RESISTANCE ( 3 FDA reports)
PATHOLOGICAL FRACTURE ( 3 FDA reports)
PERICARDIAL EFFUSION ( 3 FDA reports)
POLLAKIURIA ( 3 FDA reports)
PREMATURE BABY ( 3 FDA reports)
PSEUDOMONAL SEPSIS ( 3 FDA reports)
PYELONEPHRITIS ( 3 FDA reports)
RASH PAPULAR ( 3 FDA reports)
REFUSAL OF TREATMENT BY PATIENT ( 3 FDA reports)
RENAL DISORDER ( 3 FDA reports)
RENAL FAILURE CHRONIC ( 3 FDA reports)
RUBELLA ( 3 FDA reports)
SARCOMA ( 3 FDA reports)
SINUS TACHYCARDIA ( 3 FDA reports)
SUPRAVENTRICULAR TACHYCARDIA ( 3 FDA reports)
THROMBOCYTOPENIC PURPURA ( 3 FDA reports)
TRANSAMINASES INCREASED ( 3 FDA reports)
TREATMENT NONCOMPLIANCE ( 3 FDA reports)
TUBULOINTERSTITIAL NEPHRITIS ( 3 FDA reports)
TYPE 2 DIABETES MELLITUS ( 3 FDA reports)
VIRAL LOAD INCREASED ( 3 FDA reports)
VIRAL RASH ( 3 FDA reports)
ABORTION INDUCED ( 2 FDA reports)
ACUTE HAEMORRHAGIC CONJUNCTIVITIS ( 2 FDA reports)
AFFECT LABILITY ( 2 FDA reports)
ANHEDONIA ( 2 FDA reports)
APHTHOUS STOMATITIS ( 2 FDA reports)
ARTHRITIS ( 2 FDA reports)
ATYPICAL MYCOBACTERIAL INFECTION ( 2 FDA reports)
BLISTER ( 2 FDA reports)
BLOOD ALBUMIN ABNORMAL ( 2 FDA reports)
BLOOD ALBUMIN INCREASED ( 2 FDA reports)
BLOOD BICARBONATE ABNORMAL ( 2 FDA reports)
BLOOD CREATINE INCREASED ( 2 FDA reports)
BLOOD HIV RNA INCREASED ( 2 FDA reports)
BLOOD URINE PRESENT ( 2 FDA reports)
BONE DISORDER ( 2 FDA reports)
BONE PAIN ( 2 FDA reports)
BRAIN OEDEMA ( 2 FDA reports)
BUNDLE BRANCH BLOCK RIGHT ( 2 FDA reports)
CANDIDIASIS ( 2 FDA reports)
CARDIAC FAILURE CONGESTIVE ( 2 FDA reports)
CARDIO-RESPIRATORY ARREST ( 2 FDA reports)
CARDIOMYOPATHY ( 2 FDA reports)
CELL DEATH ( 2 FDA reports)
CENTRAL OBESITY ( 2 FDA reports)
CEREBRAL ATROPHY ( 2 FDA reports)
CERVIX OPERATION ( 2 FDA reports)
CHROMATURIA ( 2 FDA reports)
CLONUS ( 2 FDA reports)
COAGULATION TIME PROLONGED ( 2 FDA reports)
COAGULOPATHY ( 2 FDA reports)
CONGENITAL ANOMALY ( 2 FDA reports)
CONJUNCTIVITIS ( 2 FDA reports)
CONTUSION ( 2 FDA reports)
CORONARY ARTERY DISEASE ( 2 FDA reports)
CUSHINGOID ( 2 FDA reports)
CYTOMEGALOVIRUS VIRAEMIA ( 2 FDA reports)
DEEP VEIN THROMBOSIS ( 2 FDA reports)
DELIRIUM ( 2 FDA reports)
DISORIENTATION ( 2 FDA reports)
DRUG RASH WITH EOSINOPHILIA AND SYSTEMIC SYMPTOMS ( 2 FDA reports)
DYSAESTHESIA ( 2 FDA reports)
DYSURIA ( 2 FDA reports)
EAR INFECTION ( 2 FDA reports)
EPSTEIN-BARR VIRUS INFECTION ( 2 FDA reports)
EXANTHEM ( 2 FDA reports)
EYE OPERATION ( 2 FDA reports)
FANCONI SYNDROME ACQUIRED ( 2 FDA reports)
FAT TISSUE INCREASED ( 2 FDA reports)
FEMORAL NECK FRACTURE ( 2 FDA reports)
FLANK PAIN ( 2 FDA reports)
FOLATE DEFICIENCY ( 2 FDA reports)
FOOT FRACTURE ( 2 FDA reports)
GALLBLADDER DISORDER ( 2 FDA reports)
GASTRIC CANCER ( 2 FDA reports)
GASTROINTESTINAL PERFORATION ( 2 FDA reports)
GENERAL PHYSICAL CONDITION ABNORMAL ( 2 FDA reports)
GENERALISED ERYTHEMA ( 2 FDA reports)
GLOMERULAR FILTRATION RATE DECREASED ( 2 FDA reports)
HAEMODIALYSIS ( 2 FDA reports)
HAEMOLYSIS ( 2 FDA reports)
HAEMOPTYSIS ( 2 FDA reports)
HAEMORRHAGIC ASCITES ( 2 FDA reports)
HALLUCINATION ( 2 FDA reports)
HEART RATE INCREASED ( 2 FDA reports)
HEMIPLEGIA ( 2 FDA reports)
HEPATIC NEOPLASM MALIGNANT ( 2 FDA reports)
HEPATITIS CHOLESTATIC ( 2 FDA reports)
HEPATOSPLENOMEGALY ( 2 FDA reports)
HERPES SIMPLEX ( 2 FDA reports)
HYPERGLYCAEMIA ( 2 FDA reports)
HYPERREFLEXIA ( 2 FDA reports)
HYPERTENSIVE CRISIS ( 2 FDA reports)
HYPERTONIA NEONATAL ( 2 FDA reports)
HYPERVENTILATION ( 2 FDA reports)
HYPOTHYROIDISM ( 2 FDA reports)
HYPOXIC ENCEPHALOPATHY ( 2 FDA reports)
IDIOPATHIC THROMBOCYTOPENIC PURPURA ( 2 FDA reports)
INCORRECT DOSE ADMINISTERED ( 2 FDA reports)
JOINT DISLOCATION ( 2 FDA reports)
JOINT SWELLING ( 2 FDA reports)
KAWASAKI'S DISEASE ( 2 FDA reports)
LACUNAR INFARCTION ( 2 FDA reports)
LEFT VENTRICULAR HYPERTROPHY ( 2 FDA reports)
LIPOMATOSIS ( 2 FDA reports)
LUNG DISORDER ( 2 FDA reports)
LYMPHOCYTE COUNT INCREASED ( 2 FDA reports)
MANIA ( 2 FDA reports)
METASTASES TO ADRENALS ( 2 FDA reports)
METASTASES TO CENTRAL NERVOUS SYSTEM ( 2 FDA reports)
METASTASES TO LIVER ( 2 FDA reports)
METASTASES TO SKIN ( 2 FDA reports)
MICROCEPHALY ( 2 FDA reports)
MITOCHONDRIAL DNA MUTATION ( 2 FDA reports)
MULTI-ORGAN FAILURE ( 2 FDA reports)
NEONATAL DISORDER ( 2 FDA reports)
NEPHRITIS ( 2 FDA reports)
NEPHROPATHY TOXIC ( 2 FDA reports)
NEURALGIA ( 2 FDA reports)
NIGHT SWEATS ( 2 FDA reports)
NIGHTMARE ( 2 FDA reports)
NORMAL NEWBORN ( 2 FDA reports)
OESOPHAGEAL INFECTION ( 2 FDA reports)
OESOPHAGEAL VARICES HAEMORRHAGE ( 2 FDA reports)
OESOPHAGITIS ( 2 FDA reports)
ORAL DISORDER ( 2 FDA reports)
ORAL INTAKE REDUCED ( 2 FDA reports)
OSTEOPENIA ( 2 FDA reports)
PANCREATIC DISORDER ( 2 FDA reports)
PANCREATIC INSUFFICIENCY ( 2 FDA reports)
PLEURAL EFFUSION ( 2 FDA reports)
POST LUMBAR PUNCTURE SYNDROME ( 2 FDA reports)
PREMATURE SEPARATION OF PLACENTA ( 2 FDA reports)
PULMONARY OEDEMA ( 2 FDA reports)
QUALITY OF LIFE DECREASED ( 2 FDA reports)
RALES ( 2 FDA reports)
RASH GENERALISED ( 2 FDA reports)
RED BLOOD CELL COUNT DECREASED ( 2 FDA reports)
RENAL COLIC ( 2 FDA reports)
RENAL FUNCTION TEST ABNORMAL ( 2 FDA reports)
RESPIRATORY RATE INCREASED ( 2 FDA reports)
REVERSIBLE POSTERIOR LEUKOENCEPHALOPATHY SYNDROME ( 2 FDA reports)
SENSORY DISTURBANCE ( 2 FDA reports)
SEPSIS ( 2 FDA reports)
SKIN LESION ( 2 FDA reports)
STEVENS-JOHNSON SYNDROME ( 2 FDA reports)
STILLBIRTH ( 2 FDA reports)
STRONGYLOIDIASIS ( 2 FDA reports)
SUBDURAL HAEMORRHAGE ( 2 FDA reports)
SUICIDAL IDEATION ( 2 FDA reports)
SUICIDE ATTEMPT ( 2 FDA reports)
SWELLING FACE ( 2 FDA reports)
TACHYPNOEA ( 2 FDA reports)
TEARFULNESS ( 2 FDA reports)
TENDONITIS ( 2 FDA reports)
TENOSYNOVITIS ( 2 FDA reports)
TOXIC EPIDERMAL NECROLYSIS ( 2 FDA reports)
TREATMENT FAILURE ( 2 FDA reports)
TUBERCULOSIS ( 2 FDA reports)
URETERIC DILATATION ( 2 FDA reports)
URTICARIA ( 2 FDA reports)
VASCULITIS ( 2 FDA reports)
VASODILATATION ( 2 FDA reports)
VIRAL MUTATION IDENTIFIED ( 2 FDA reports)
VIROLOGIC FAILURE ( 2 FDA reports)
VISION BLURRED ( 2 FDA reports)
WEGENER'S GRANULOMATOSIS ( 2 FDA reports)
ABASIA ( 1 FDA reports)
ABDOMINAL ABSCESS ( 1 FDA reports)
ACCIDENT ( 1 FDA reports)
ACCIDENTAL OVERDOSE ( 1 FDA reports)
ACIDOSIS ( 1 FDA reports)
ACQUIRED IMMUNODEFICIENCY SYNDROME ( 1 FDA reports)
ACUTE CORONARY SYNDROME ( 1 FDA reports)
ACUTE GENERALISED EXANTHEMATOUS PUSTULOSIS ( 1 FDA reports)
ACUTE MYELOID LEUKAEMIA ( 1 FDA reports)
ACUTE MYOCARDIAL INFARCTION ( 1 FDA reports)
ACUTE RESPIRATORY DISTRESS SYNDROME ( 1 FDA reports)
ADENOMYOSIS ( 1 FDA reports)
ADRENAL INSUFFICIENCY ( 1 FDA reports)
ADRENAL SUPPRESSION ( 1 FDA reports)
ADVERSE DRUG REACTION ( 1 FDA reports)
AIDS RELATED COMPLICATION ( 1 FDA reports)
ALANINE AMINOTRANSFERASE ABNORMAL ( 1 FDA reports)
ALLERGIC GRANULOMATOUS ANGIITIS ( 1 FDA reports)
ALTERED STATE OF CONSCIOUSNESS ( 1 FDA reports)
ALVEOLITIS ( 1 FDA reports)
AMNIOTIC FLUID VOLUME DECREASED ( 1 FDA reports)
ANAEMIA HAEMOLYTIC AUTOIMMUNE ( 1 FDA reports)
ANAEMIA NEONATAL ( 1 FDA reports)
ANAEMIA OF CHRONIC DISEASE ( 1 FDA reports)
ANAEMIA POSTOPERATIVE ( 1 FDA reports)
ANAL NEOPLASM ( 1 FDA reports)
ANALGESIC DRUG LEVEL DECREASED ( 1 FDA reports)
ANALGESIC DRUG LEVEL INCREASED ( 1 FDA reports)
ANDROGEN DEFICIENCY ( 1 FDA reports)
ANGINA PECTORIS ( 1 FDA reports)
ANGIOEDEMA ( 1 FDA reports)
ANGIOPATHY ( 1 FDA reports)
ANTERIOR INTEROSSEOUS SYNDROME ( 1 FDA reports)
ANTIBODY TEST POSITIVE ( 1 FDA reports)
AORTIC ARTERIOSCLEROSIS ( 1 FDA reports)
APLASTIC ANAEMIA ( 1 FDA reports)
APPENDICECTOMY ( 1 FDA reports)
ARTERIAL OCCLUSIVE DISEASE ( 1 FDA reports)
ASEPTIC NECROSIS BONE ( 1 FDA reports)
ASTROCYTOMA ( 1 FDA reports)
ATELECTASIS ( 1 FDA reports)
AZOTAEMIA ( 1 FDA reports)
BACILLARY ANGIOMATOSIS ( 1 FDA reports)
BACTERAEMIA ( 1 FDA reports)
BARRETT'S OESOPHAGUS ( 1 FDA reports)
BETA 2 MICROGLOBULIN URINE INCREASED ( 1 FDA reports)
BIOPSY BONE MARROW ABNORMAL ( 1 FDA reports)
BLOOD ALBUMIN DECREASED ( 1 FDA reports)
BLOOD ALKALINE PHOSPHATASE ABNORMAL ( 1 FDA reports)
BLOOD BICARBONATE DECREASED ( 1 FDA reports)
BLOOD CREATININE DECREASED ( 1 FDA reports)
BLOOD DISORDER ( 1 FDA reports)
BLOOD GLUCOSE ABNORMAL ( 1 FDA reports)
BLOOD GLUCOSE INCREASED ( 1 FDA reports)
BLOOD IRON INCREASED ( 1 FDA reports)
BLOOD PH DECREASED ( 1 FDA reports)
BLOOD PHOSPHORUS INCREASED ( 1 FDA reports)
BLOOD PRESSURE DECREASED ( 1 FDA reports)
BLOOD PRESSURE IMMEASURABLE ( 1 FDA reports)
BLOOD PRESSURE SYSTOLIC INSPIRATORY DECREASED ( 1 FDA reports)
BLOOD TRIGLYCERIDES ABNORMAL ( 1 FDA reports)
BLOOD UREA INCREASED ( 1 FDA reports)
BODY TEMPERATURE DECREASED ( 1 FDA reports)
BREAST MASS ( 1 FDA reports)
BREECH DELIVERY ( 1 FDA reports)
BRONCHIAL CARCINOMA ( 1 FDA reports)
BRONCHIAL DISORDER ( 1 FDA reports)
BRONCHIAL WALL THICKENING ( 1 FDA reports)
BRONCHOSCOPY ABNORMAL ( 1 FDA reports)
BRONCHOSPASM ( 1 FDA reports)
BURNING SENSATION ( 1 FDA reports)
BURSITIS ( 1 FDA reports)
CAMPYLOBACTER INTESTINAL INFECTION ( 1 FDA reports)
CARDIAC DISORDER ( 1 FDA reports)
CARDIOGENIC SHOCK ( 1 FDA reports)
CARDIOLIPIN ANTIBODY POSITIVE ( 1 FDA reports)
CARDIOTHORACIC RATIO INCREASED ( 1 FDA reports)
CD4 LYMPHOCYTES INCREASED ( 1 FDA reports)
CD8 LYMPHOCYTES DECREASED ( 1 FDA reports)
CD8 LYMPHOCYTES INCREASED ( 1 FDA reports)
CELLULITIS ( 1 FDA reports)
CENTRAL-ALVEOLAR HYPOVENTILATION ( 1 FDA reports)
CEREBROVASCULAR DISORDER ( 1 FDA reports)
CERVICAL DYSPLASIA ( 1 FDA reports)
CHROMOSOMAL MUTATION ( 1 FDA reports)
CHRONIC ALLOGRAFT NEPHROPATHY ( 1 FDA reports)
CHRONIC FATIGUE SYNDROME ( 1 FDA reports)
CHRONIC OBSTRUCTIVE PULMONARY DISEASE ( 1 FDA reports)
COLD SWEAT ( 1 FDA reports)
COLITIS ( 1 FDA reports)
COLITIS ULCERATIVE ( 1 FDA reports)
COMA ( 1 FDA reports)
COMPLETED SUICIDE ( 1 FDA reports)
CONCOMITANT DISEASE AGGRAVATED ( 1 FDA reports)
CONJUNCTIVAL HYPERAEMIA ( 1 FDA reports)
CRANIOCEREBRAL INJURY ( 1 FDA reports)
CREATININE RENAL CLEARANCE INCREASED ( 1 FDA reports)
CRYING ( 1 FDA reports)
CRYPTOCOCCOSIS ( 1 FDA reports)
CRYPTOGENIC ORGANISING PNEUMONIA ( 1 FDA reports)
CSF PROTEIN INCREASED ( 1 FDA reports)
DIABETES MELLITUS INADEQUATE CONTROL ( 1 FDA reports)
DIABETIC RETINOPATHY ( 1 FDA reports)
DIVERTICULITIS ( 1 FDA reports)
DIVERTICULUM DUODENAL ( 1 FDA reports)
DIVERTICULUM INTESTINAL ( 1 FDA reports)
DRUG EFFECT DECREASED ( 1 FDA reports)
DRUG-INDUCED LIVER INJURY ( 1 FDA reports)
DRY SKIN ( 1 FDA reports)
DYSPNOEA EXERTIONAL ( 1 FDA reports)
EAR MALFORMATION ( 1 FDA reports)
ECCHYMOSIS ( 1 FDA reports)
ECONOMIC PROBLEM ( 1 FDA reports)
ELECTROCARDIOGRAM ABNORMAL ( 1 FDA reports)
ELECTROENCEPHALOGRAM ABNORMAL ( 1 FDA reports)
ENANTHEMA ( 1 FDA reports)
EROSIVE OESOPHAGITIS ( 1 FDA reports)
ESCHERICHIA INFECTION ( 1 FDA reports)
ESCHERICHIA SEPSIS ( 1 FDA reports)
FACIAL PALSY ( 1 FDA reports)
FAECAL INCONTINENCE ( 1 FDA reports)
FANCONI SYNDROME ( 1 FDA reports)
FAT ATROPHY ( 1 FDA reports)
FEAR ( 1 FDA reports)
FEMUR FRACTURE ( 1 FDA reports)
FIBRIN D DIMER INCREASED ( 1 FDA reports)
FIBROSARCOMA ( 1 FDA reports)
FISTULA ( 1 FDA reports)
FOETAL GROWTH RETARDATION ( 1 FDA reports)
FOLLICULITIS ( 1 FDA reports)
FOOD INTOLERANCE ( 1 FDA reports)
FUNGUS CSF TEST POSITIVE ( 1 FDA reports)
GASTRIC ULCER ( 1 FDA reports)
GASTRITIS ( 1 FDA reports)
GASTROENTERITIS SALMONELLA ( 1 FDA reports)
GASTROINTESTINAL HAEMORRHAGE ( 1 FDA reports)
GASTROINTESTINAL TOXICITY ( 1 FDA reports)
GAZE PALSY ( 1 FDA reports)
GENITAL HERPES ( 1 FDA reports)
GLAUCOMA ( 1 FDA reports)
GLOMERULONEPHRITIS ( 1 FDA reports)
GLOMERULONEPHRITIS MEMBRANOUS ( 1 FDA reports)
GLUCOSE TOLERANCE IMPAIRED ( 1 FDA reports)
GROIN PAIN ( 1 FDA reports)
HAEMANGIOMA ( 1 FDA reports)
HAEMATEMESIS ( 1 FDA reports)
HAEMOGLOBIN INCREASED ( 1 FDA reports)
HAEMOGLOBINURIA ( 1 FDA reports)
HAPTOGLOBIN INCREASED ( 1 FDA reports)
HBV DNA INCREASED ( 1 FDA reports)
HEPATIC CONGESTION ( 1 FDA reports)
HEPATITIS ACUTE ( 1 FDA reports)
HEPATITIS B DNA INCREASED ( 1 FDA reports)
HEPATITIS C ( 1 FDA reports)
HEPATITIS TOXIC ( 1 FDA reports)
HEPATITIS VIRAL ( 1 FDA reports)
HEPATOBILIARY SCAN ABNORMAL ( 1 FDA reports)
HEPATOCELLULAR INJURY ( 1 FDA reports)
HERNIA REPAIR ( 1 FDA reports)
HERPES VIRUS INFECTION ( 1 FDA reports)
HILAR LYMPHADENOPATHY ( 1 FDA reports)
HISTOPLASMOSIS DISSEMINATED ( 1 FDA reports)
HIV TEST POSITIVE ( 1 FDA reports)
HODGKIN'S DISEASE ( 1 FDA reports)
HOT FLUSH ( 1 FDA reports)
HYPERAESTHESIA ( 1 FDA reports)
HYPERCORTICOIDISM ( 1 FDA reports)
HYPERKALAEMIA ( 1 FDA reports)
HYPERURICAEMIA ( 1 FDA reports)
HYPOGEUSIA ( 1 FDA reports)
HYPOGONADISM ( 1 FDA reports)
HYPOKINESIA ( 1 FDA reports)
HYPOMAGNESAEMIA ( 1 FDA reports)
HYPOVOLAEMIA ( 1 FDA reports)
HYPOXIA ( 1 FDA reports)
ILEUS ( 1 FDA reports)
IMMUNE SYSTEM DISORDER ( 1 FDA reports)
INCOHERENT ( 1 FDA reports)
INFECTION ( 1 FDA reports)
INJECTION SITE ERYTHEMA ( 1 FDA reports)
INSULIN RESISTANCE ( 1 FDA reports)
INTERNATIONAL NORMALISED RATIO INCREASED ( 1 FDA reports)
INTRA-ABDOMINAL HAEMATOMA ( 1 FDA reports)
JC VIRUS INFECTION ( 1 FDA reports)
JOINT EFFUSION ( 1 FDA reports)
KETOACIDOSIS ( 1 FDA reports)
LEFT VENTRICULAR FAILURE ( 1 FDA reports)
LEPROSY ( 1 FDA reports)
LETHARGY ( 1 FDA reports)
LEUKOCYTOCLASTIC VASCULITIS ( 1 FDA reports)
LEUKOENCEPHALOPATHY ( 1 FDA reports)
LIP SWELLING ( 1 FDA reports)
LIPID METABOLISM DISORDER ( 1 FDA reports)
LIVEDO RETICULARIS ( 1 FDA reports)
LUNG NEOPLASM MALIGNANT ( 1 FDA reports)
LYMPH NODE CALCIFICATION ( 1 FDA reports)
LYMPH NODE PAIN ( 1 FDA reports)
LYMPH NODE PALPABLE ( 1 FDA reports)
LYMPHOCYTE MORPHOLOGY ABNORMAL ( 1 FDA reports)
LYMPHOPENIA ( 1 FDA reports)
MAJOR DEPRESSION ( 1 FDA reports)
MELAENA ( 1 FDA reports)
MENINGITIS CRYPTOCOCCAL ( 1 FDA reports)
MENINGITIS FUNGAL ( 1 FDA reports)
MENINGITIS STAPHYLOCOCCAL ( 1 FDA reports)
MENTAL DISORDER ( 1 FDA reports)
METABOLIC SYNDROME ( 1 FDA reports)
MICROCYTIC ANAEMIA ( 1 FDA reports)
MITOCHONDRIAL CYTOPATHY ( 1 FDA reports)
MITOCHONDRIAL DNA DELETION ( 1 FDA reports)
MONONEUROPATHY ( 1 FDA reports)
MOUTH ULCERATION ( 1 FDA reports)
MYCOBACTERIAL INFECTION ( 1 FDA reports)
MYOPIA ( 1 FDA reports)
NASAL SEPTUM DEVIATION ( 1 FDA reports)
NECROSIS ( 1 FDA reports)
NEURALGIC AMYOTROPHY ( 1 FDA reports)
NEUROLOGICAL SYMPTOM ( 1 FDA reports)
ODYNOPHAGIA ( 1 FDA reports)
OFF LABEL USE ( 1 FDA reports)
OLIGODENDROGLIOMA ( 1 FDA reports)
OLIGOHYDRAMNIOS ( 1 FDA reports)
OPTIC NEURITIS RETROBULBAR ( 1 FDA reports)
OPTIC NEUROPATHY ( 1 FDA reports)
OROPHARYNGEAL CANDIDIASIS ( 1 FDA reports)
OROPHARYNGEAL PAIN ( 1 FDA reports)
OSTEOARTHRITIS ( 1 FDA reports)
OSTEOPOROSIS ( 1 FDA reports)
OSTEOPOROTIC FRACTURE ( 1 FDA reports)
OVERDOSE ( 1 FDA reports)
PALMAR ERYTHEMA ( 1 FDA reports)
PANIC ATTACK ( 1 FDA reports)
PAPILLOMA VIRAL INFECTION ( 1 FDA reports)
PARTIAL SEIZURES ( 1 FDA reports)
PARTNER STRESS ( 1 FDA reports)
PATENT DUCTUS ARTERIOSUS ( 1 FDA reports)
PELVI-URETERIC OBSTRUCTION ( 1 FDA reports)
PENIS DISORDER ( 1 FDA reports)
PERFORATED ULCER ( 1 FDA reports)
PERICARDIAL HAEMORRHAGE ( 1 FDA reports)
PERIPHERAL NERVE PALSY ( 1 FDA reports)
PERITONITIS ( 1 FDA reports)
PHARYNGITIS BACTERIAL ( 1 FDA reports)
PHLEBITIS ( 1 FDA reports)
PHLEBOTOMY ( 1 FDA reports)
PLEURITIC PAIN ( 1 FDA reports)
PNEUMOCOCCAL SEPSIS ( 1 FDA reports)
PNEUMONIA CYTOMEGALOVIRAL ( 1 FDA reports)
PNEUMONIA LEGIONELLA ( 1 FDA reports)
PNEUMONIA PNEUMOCOCCAL ( 1 FDA reports)
PNEUMONIA PRIMARY ATYPICAL ( 1 FDA reports)
PNEUMONIA STREPTOCOCCAL ( 1 FDA reports)
PNEUMONITIS ( 1 FDA reports)
PORTAL HYPERTENSION ( 1 FDA reports)
PORTAL VEIN THROMBOSIS ( 1 FDA reports)
POSTOPERATIVE FEVER ( 1 FDA reports)
PROCEDURAL HAEMORRHAGE ( 1 FDA reports)
PRODUCT QUALITY ISSUE ( 1 FDA reports)
PROTEIN S DEFICIENCY ( 1 FDA reports)
PROTEIN URINE PRESENT ( 1 FDA reports)
PROTHROMBIN TIME PROLONGED ( 1 FDA reports)
PSEUDOMONAS INFECTION ( 1 FDA reports)
PSORIASIS ( 1 FDA reports)
PSYCHOMOTOR HYPERACTIVITY ( 1 FDA reports)
PSYCHOTIC DISORDER ( 1 FDA reports)
PULMONARY CALCIFICATION ( 1 FDA reports)
PULMONARY HAEMORRHAGE ( 1 FDA reports)
RASH PUSTULAR ( 1 FDA reports)
RASH VESICULAR ( 1 FDA reports)
RECTAL DISCHARGE ( 1 FDA reports)
RED BLOOD CELL ABNORMALITY ( 1 FDA reports)
RED BLOOD CELLS URINE ( 1 FDA reports)
RESPIRATORY ALKALOSIS ( 1 FDA reports)
RESTLESSNESS ( 1 FDA reports)
RETINOPATHY ( 1 FDA reports)
SALIVARY HYPERSECRETION ( 1 FDA reports)
SCAB ( 1 FDA reports)
SCAR ( 1 FDA reports)
SKIN DISORDER ( 1 FDA reports)
SKIN STRIAE ( 1 FDA reports)
SMALL CELL CARCINOMA ( 1 FDA reports)
SMALL CELL LUNG CANCER STAGE UNSPECIFIED ( 1 FDA reports)
SMOKER ( 1 FDA reports)
SPLENIC CALCIFICATION ( 1 FDA reports)
STATUS EPILEPTICUS ( 1 FDA reports)
STEATORRHOEA ( 1 FDA reports)
STILL'S DISEASE ADULT ONSET ( 1 FDA reports)
STOMACH DISCOMFORT ( 1 FDA reports)
SUBCUTANEOUS ABSCESS ( 1 FDA reports)
SUPRAPUBIC PAIN ( 1 FDA reports)
SYNCOPE ( 1 FDA reports)
SYNOVITIS ( 1 FDA reports)
TARDIVE DYSKINESIA ( 1 FDA reports)
TETANY ( 1 FDA reports)
THERAPEUTIC PRODUCT CONTAMINATION ( 1 FDA reports)
THROMBOCYTHAEMIA ( 1 FDA reports)
THROMBOSIS ( 1 FDA reports)
TORSADE DE POINTES ( 1 FDA reports)
TOXIC SKIN ERUPTION ( 1 FDA reports)
TOXOPLASMOSIS ( 1 FDA reports)
TRANSIENT ISCHAEMIC ATTACK ( 1 FDA reports)
TRIGEMINAL NEURALGIA ( 1 FDA reports)
TWIN PREGNANCY ( 1 FDA reports)
TYPE 1 DIABETES MELLITUS ( 1 FDA reports)
UNEVALUABLE EVENT ( 1 FDA reports)
UPPER RESPIRATORY TRACT INFECTION ( 1 FDA reports)
URETHRAL DISCHARGE ( 1 FDA reports)
URINARY INCONTINENCE ( 1 FDA reports)
URINARY RETENTION ( 1 FDA reports)
URINARY TRACT INFECTION ( 1 FDA reports)
URINE ABNORMALITY ( 1 FDA reports)
URINE OUTPUT DECREASED ( 1 FDA reports)
URINE PHOSPHATE DECREASED ( 1 FDA reports)
UVEITIS ( 1 FDA reports)
VARICES OESOPHAGEAL ( 1 FDA reports)
VENOUS PRESSURE JUGULAR INCREASED ( 1 FDA reports)
VIRAEMIA ( 1 FDA reports)
VIRAL LOAD DECREASED ( 1 FDA reports)
VISUAL ACUITY REDUCED ( 1 FDA reports)
VITAMIN D DECREASED ( 1 FDA reports)
WHEELCHAIR USER ( 1 FDA reports)
WHITE BLOOD CELL COUNT INCREASED ( 1 FDA reports)
ZYGOMYCOSIS ( 1 FDA reports)

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