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
117297422 11729742 2 F 2015 20160825 20151112 20160831 EXP US-PFIZER INC-2015382963 PFIZER 59.00 YR F Y 0.00000 20160831 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
117297422 11729742 1 PS REVATIO SILDENAFIL CITRATE 1 20 MG, 3X/DAY 21845 20 MG FILM-COATED TABLET TID
117297422 11729742 2 SS REVATIO SILDENAFIL CITRATE 1 40 MG, 3X/DAY 21845 40 MG FILM-COATED TABLET TID
117297422 11729742 3 SS REVATIO SILDENAFIL CITRATE 1 DOSE WAS DECREASED 21845 FILM-COATED TABLET

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
117297422 11729742 1 Catheterisation cardiac
117297422 11729742 2 Pulmonary hypertension

Outcome of event

Event ID CASEID OUTC COD
117297422 11729742 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
117297422 11729742 Asthma
117297422 11729742 Condition aggravated
117297422 11729742 Product use issue
117297422 11729742 Pulmonary hypertension

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
117297422 11729742 1 201509 0
117297422 11729742 2 2015 0