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
126070372 12607037 2 F 20160721 20160907 20160729 20160909 EXP US-PFIZER INC-2016362866 PFIZER 92.00 YR F Y 0.00000 20160909 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
126070372 12607037 1 PS REVATIO SILDENAFIL CITRATE 1 20 MG, 3X/DAY 21845 20 MG FILM-COATED TABLET TID
126070372 12607037 2 SS REVATIO SILDENAFIL CITRATE 1 20 MG, 2X/DAY 21845 20 MG FILM-COATED TABLET BID
126070372 12607037 3 SS REVATIO SILDENAFIL CITRATE 1 20 MG, 1X/DAY 21845 20 MG FILM-COATED TABLET QD
126070372 12607037 4 C DIGOXIN. DIGOXIN 1 UNK 0
126070372 12607037 5 C LACTULOSE. LACTULOSE 1 UNK 0
126070372 12607037 6 C XANAX ALPRAZOLAM 1 UNK 0
126070372 12607037 7 C ROXANOL MORPHINE SULFATE 1 UNK 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126070372 12607037 1 Pulmonary hypertension

Outcome of event

Event ID CASEID OUTC COD
126070372 12607037 DE
126070372 12607037 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
126070372 12607037 Death

Reporting Sources (this data is often not reported and may therefore be missing here)

no results found

Therapies reported

no results found