The Safety Rates Drug Report

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Drug     Injury     Quarter    

Person who experienced the adverse event (patient)

Event ID CASEID CASEVERSION I F COD EVENT DT MFR DT INIT FDA DT FDA DT REPT COD AUTH NUM MFR NUM MFR SNDR LIT REF AGE AGE COD AGE GRP GNDR COD E SUB WT WT COD REPT DT TO MFR OCCP COD REPORTER COUNTRY OCCR COUNTRY
125244584 12524458 4 F 20160705 20160713 20160704 20160719 EXP US-GILEAD-2016-0221504 GILEAD 66.00 YR E F Y 61.20000 KG 20160719 CN US US

Drug(s) used by person

Event ID CASEID DRUG SEQ ROLE COD DRUGNAME PROD AI VAL VBM ROUTE DOSE VBM CUM DOSE CHR CUM DOSE UNIT DECHAL RECHAL LOT NUM EXP DT NDA NUM DOSE AMT DOSE UNIT DOSE FORM DOSE FREQ
125244584 12524458 1 PS AMBRISENTAN AMBRISENTAN 1 Unknown 5 MG, QD 1412805A 22081 5 MG TABLET QD
125244584 12524458 2 SS REMODULIN TREPROSTINIL 1 Unknown 0.046 UG/KG, UNK U 2100910 0 .046 UG/KG INJECTION
125244584 12524458 3 C ADCIRCA TADALAFIL 1 0
125244584 12524458 4 C COUMADIN WARFARIN SODIUM 1 0
125244584 12524458 5 C PREDNISONE. PREDNISONE 1 0
125244584 12524458 6 C LASIX FUROSEMIDE 1 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125244584 12524458 1 Product used for unknown indication
125244584 12524458 2 Pulmonary arterial hypertension

Outcome of event

Event ID CASEID OUTC COD
125244584 12524458 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
125244584 12524458 Asthenia
125244584 12524458 Cough
125244584 12524458 Diarrhoea
125244584 12524458 Feeling abnormal
125244584 12524458 Flushing
125244584 12524458 Hypoxia
125244584 12524458 Pallor
125244584 12524458 Presyncope
125244584 12524458 Vomiting

Reporting Sources (this data is often not reported and may therefore be missing here)

no results found

Therapies reported

Event ID CASEID DSG DRUG SEQ START DT END DT DUR DUR COD
125244584 12524458 2 20150708 0