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
100105584 10010558 4 F 20140228 20160829 20140314 20160906 EXP US-PFIZER INC-2014070469 PFIZER 83.00 YR F Y 68.27000 KG 20160906 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
100105584 10010558 1 PS REVATIO SILDENAFIL CITRATE 1 Oral 20 MG, 3X/DAY A382301 21845 20 MG FILM-COATED TABLET TID

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
100105584 10010558 1 Pulmonary hypertension

Outcome of event

Event ID CASEID OUTC COD
100105584 10010558 HO
100105584 10010558 DE

Reactions reported

Event ID CASEID DRUG REC ACT PT
100105584 10010558 Blood sodium increased
100105584 10010558 Cardiac failure congestive
100105584 10010558 Death
100105584 10010558 Disease progression
100105584 10010558 Dysphagia
100105584 10010558 Fluid retention
100105584 10010558 Haemoglobin decreased
100105584 10010558 Oxygen saturation decreased
100105584 10010558 Respiratory arrest
100105584 10010558 Weight increased

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
100105584 10010558 1 2011 20160821 0