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
127455502 12745550 2 F 20160914 20160915 20160919 EXP US-GILEAD-2016-0230577 GILEAD 47.00 YR A F Y 0.00000 20160919 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
127455502 12745550 1 PS AMBRISENTAN AMBRISENTAN 1 Unknown 5 MG, QD 1413180A 22081 5 MG TABLET QD
127455502 12745550 2 SS FLOLAN EPOPROSTENOL SODIUM 1 Unknown 0
127455502 12745550 3 C SILDENAFIL. SILDENAFIL 1 0
127455502 12745550 4 C COUMADIN WARFARIN SODIUM 1 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
127455502 12745550 1 Product used for unknown indication
127455502 12745550 2 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
127455502 12745550 HO
127455502 12745550 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
127455502 12745550 Device related infection
127455502 12745550 Flushing
127455502 12745550 Lethargy
127455502 12745550 Oxygen saturation decreased
127455502 12745550 Weight decreased

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
127455502 12745550 1 20160504 0