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

ANAEMIA ( 9 FDA reports)
DIARRHOEA ( 8 FDA reports)
CEREBRAL TOXOPLASMOSIS ( 6 FDA reports)
ACUTE RESPIRATORY FAILURE ( 5 FDA reports)
ANOREXIA ( 5 FDA reports)
C-REACTIVE PROTEIN INCREASED ( 5 FDA reports)
DISSEMINATED INTRAVASCULAR COAGULATION ( 5 FDA reports)
EATING DISORDER ( 5 FDA reports)
ENCEPHALITIS ( 5 FDA reports)
ENCEPHALITIS CYTOMEGALOVIRUS ( 5 FDA reports)
HAEMOGLOBIN DECREASED ( 5 FDA reports)
HEART DISEASE CONGENITAL ( 5 FDA reports)
HYPERTHERMIA ( 5 FDA reports)
IMMUNE RECONSTITUTION SYNDROME ( 5 FDA reports)
LOSS OF CONSCIOUSNESS ( 5 FDA reports)
MENINGISM ( 5 FDA reports)
MUSCULOSKELETAL STIFFNESS ( 5 FDA reports)
PANCYTOPENIA ( 5 FDA reports)
PLEURAL ADHESION ( 5 FDA reports)
PNEUMOTHORAX ( 5 FDA reports)
RESPIRATORY ARREST ( 5 FDA reports)
SEPSIS ( 5 FDA reports)
SHOCK ( 5 FDA reports)
STAPHYLOCOCCAL INFECTION ( 5 FDA reports)
VOMITING ( 5 FDA reports)
ASTHENIA ( 4 FDA reports)
BLOOD TRIGLYCERIDES INCREASED ( 4 FDA reports)
BONE MARROW FAILURE ( 4 FDA reports)
DRUG INTOLERANCE ( 4 FDA reports)
GENERAL PHYSICAL HEALTH DETERIORATION ( 4 FDA reports)
HALLUCINATION ( 4 FDA reports)
HYPOALBUMINAEMIA ( 4 FDA reports)
PNEUMOCYSTIS JIROVECI PNEUMONIA ( 4 FDA reports)
ARTHRALGIA ( 3 FDA reports)
CACHEXIA ( 3 FDA reports)
CHILLS ( 3 FDA reports)
DYSPNOEA ( 3 FDA reports)
HEADACHE ( 3 FDA reports)
HYPERLIPIDAEMIA ( 3 FDA reports)
KAPOSI'S SARCOMA ( 3 FDA reports)
NAUSEA ( 3 FDA reports)
PNEUMONIA ( 3 FDA reports)
PULMONARY ARTERY ATRESIA ( 3 FDA reports)
RENAL FAILURE ( 3 FDA reports)
TRICUSPID VALVE INCOMPETENCE ( 3 FDA reports)
ABDOMINAL PAIN UPPER ( 2 FDA reports)
AIDS ENCEPHALOPATHY ( 2 FDA reports)
ATYPICAL MYCOBACTERIAL INFECTION ( 2 FDA reports)
ATYPICAL MYCOBACTERIAL LYMPHADENITIS ( 2 FDA reports)
BLOOD ALKALINE PHOSPHATASE INCREASED ( 2 FDA reports)
BLOOD BILIRUBIN INCREASED ( 2 FDA reports)
BLOOD DISORDER ( 2 FDA reports)
BLOOD URIC ACID INCREASED ( 2 FDA reports)
CD4 LYMPHOCYTES DECREASED ( 2 FDA reports)
CRYPTOCOCCOSIS ( 2 FDA reports)
DEHYDRATION ( 2 FDA reports)
DEPRESSION ( 2 FDA reports)
DRUG EXPOSURE DURING PREGNANCY ( 2 FDA reports)
DRUG INTERACTION ( 2 FDA reports)
DYSPHAGIA ( 2 FDA reports)
GAMMA-GLUTAMYLTRANSFERASE INCREASED ( 2 FDA reports)
GASTROINTESTINAL DISORDER ( 2 FDA reports)
GUILLAIN-BARRE SYNDROME ( 2 FDA reports)
HEPATIC FUNCTION ABNORMAL ( 2 FDA reports)
HEPATIC STEATOSIS ( 2 FDA reports)
INFECTION ( 2 FDA reports)
INFLUENZA LIKE ILLNESS ( 2 FDA reports)
INSOMNIA ( 2 FDA reports)
LIPODYSTROPHY ACQUIRED ( 2 FDA reports)
LIVER DISORDER ( 2 FDA reports)
LYMPHOMA ( 2 FDA reports)
NEPHRITIS INTERSTITIAL ( 2 FDA reports)
NEPHROTIC SYNDROME ( 2 FDA reports)
NEUROPATHY PERIPHERAL ( 2 FDA reports)
OESOPHAGEAL CANDIDIASIS ( 2 FDA reports)
PAIN ( 2 FDA reports)
PAIN IN EXTREMITY ( 2 FDA reports)
PNEUMONIA PNEUMOCOCCAL ( 2 FDA reports)
PRODUCTIVE COUGH ( 2 FDA reports)
PROGRESSIVE MULTIFOCAL LEUKOENCEPHALOPATHY ( 2 FDA reports)
TREMOR ( 2 FDA reports)
VIRAL LOAD INCREASED ( 2 FDA reports)
VISUAL FIELD DEFECT ( 2 FDA reports)
WEIGHT DECREASED ( 2 FDA reports)
WHITE BLOOD CELL COUNT DECREASED ( 2 FDA reports)
ABORTION INDUCED ( 1 FDA reports)
ACTIVITIES OF DAILY LIVING IMPAIRED ( 1 FDA reports)
AIDS RELATED COMPLICATION ( 1 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 1 FDA reports)
ASCITES ( 1 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 1 FDA reports)
BLOOD AMYLASE INCREASED ( 1 FDA reports)
BONE FISSURE ( 1 FDA reports)
CARDIAC MURMUR ( 1 FDA reports)
CONGENITAL ANOMALY ( 1 FDA reports)
CONSTIPATION ( 1 FDA reports)
COUGH ( 1 FDA reports)
CYTOLYTIC HEPATITIS ( 1 FDA reports)
CYTOMEGALOVIRUS CHORIORETINITIS ( 1 FDA reports)
DEATH ( 1 FDA reports)
DECREASED ACTIVITY ( 1 FDA reports)
DIABETES MELLITUS ( 1 FDA reports)
DYSPEPSIA ( 1 FDA reports)
ERYTHEMA NODOSUM ( 1 FDA reports)
FANCONI SYNDROME ( 1 FDA reports)
FEELING HOT ( 1 FDA reports)
HEPATITIS ( 1 FDA reports)
HEPATITIS FULMINANT ( 1 FDA reports)
IMPAIRED SELF-CARE ( 1 FDA reports)
KETOACIDOSIS ( 1 FDA reports)
LACTIC ACIDOSIS ( 1 FDA reports)
LIVER FUNCTION TEST ABNORMAL ( 1 FDA reports)
LYMPHADENOPATHY ( 1 FDA reports)
MALAISE ( 1 FDA reports)
MENTAL DISORDER ( 1 FDA reports)
OVERDOSE ( 1 FDA reports)
PALPITATIONS ( 1 FDA reports)
PANCREATITIS ACUTE ( 1 FDA reports)
PLATELET COUNT DECREASED ( 1 FDA reports)
POST PROCEDURAL HAEMORRHAGE ( 1 FDA reports)
PREMATURE BABY ( 1 FDA reports)
RED BLOOD CELL COUNT DECREASED ( 1 FDA reports)
RENAL DISORDER ( 1 FDA reports)
RHINORRHOEA ( 1 FDA reports)
SKIN DISORDER ( 1 FDA reports)
SPEECH DISORDER ( 1 FDA reports)
TONSILLITIS ( 1 FDA reports)

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