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
125486122 12548612 2 F 20160713 20160725 20160712 20160729 EXP US-GILEAD-2016-0223223 GILEAD 59.00 YR A F Y 0.00000 20160729 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
125486122 12548612 1 PS AMBRISENTAN AMBRISENTAN 1 Unknown 10 MG, QD 1509427A 22081 10 MG TABLET QD
125486122 12548612 2 SS ADCIRCA TADALAFIL 1 Unknown N 0
125486122 12548612 3 C VENTAVIS ILOPROST 1 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125486122 12548612 1 Product used for unknown indication
125486122 12548612 2 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
125486122 12548612 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
125486122 12548612 Dyspnoea
125486122 12548612 Fluid retention
125486122 12548612 Malaise
125486122 12548612 Nephrolithiasis
125486122 12548612 Renal surgery
125486122 12548612 Urinary tract infection

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
125486122 12548612 1 20110128 0