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
117469013 11746901 3 F 2005 20160713 20151117 20160719 EXP US-PFIZER INC-2015385119 PFIZER 60.00 YR F Y 54.00000 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
117469013 11746901 1 PS REVATIO SILDENAFIL CITRATE 1 20 MG, 3X/DAY 21845 20 MG FILM-COATED TABLET TID
117469013 11746901 2 SS REVATIO SILDENAFIL CITRATE 1 ONE TAB 20 MG DAILY (INSTEAD OF TWO TABS 3 TIMES DAILY) 21845 20 MG FILM-COATED TABLET
117469013 11746901 3 C LETAIRIS AMBRISENTAN 1 UNK 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
117469013 11746901 1 Pulmonary hypertension

Outcome of event

Event ID CASEID OUTC COD
117469013 11746901 HO
117469013 11746901 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
117469013 11746901 Aspiration
117469013 11746901 Gastrooesophageal reflux disease
117469013 11746901 Intentional product use issue
117469013 11746901 Pneumonia bacterial

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
117469013 11746901 1 2005 0
117469013 11746901 3 2006 0