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
124814414 12481441 4 F 20160615 20160808 20160620 20160811 EXP US-GILEAD-2016-0216535 GILEAD 81.00 YR E F Y 0.00000 20160811 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
124814414 12481441 1 PS AMBRISENTAN AMBRISENTAN 1 Unknown 5 MG, QD 1413180A 22081 5 MG TABLET QD
124814414 12481441 2 SS ADEMPAS RIOCIGUAT 1 Unknown UNK 0
124814414 12481441 3 SS ADEMPAS RIOCIGUAT 1 Unknown 0.5 MG, UNK 0 .5 MG
124814414 12481441 4 SS ADEMPAS RIOCIGUAT 1 Unknown 1 MG, TID 0 1 MG TID
124814414 12481441 5 SS ADCIRCA TADALAFIL 1 Unknown UNK U 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
124814414 12481441 1 Product used for unknown indication
124814414 12481441 2 Product used for unknown indication
124814414 12481441 5 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
124814414 12481441 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
124814414 12481441 Abdominal pain
124814414 12481441 Chest discomfort
124814414 12481441 Chest pain
124814414 12481441 Deafness
124814414 12481441 Fatigue
124814414 12481441 Hypotension
124814414 12481441 Oedema
124814414 12481441 Oedema peripheral

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
124814414 12481441 1 20151021 0