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
126688982 12668898 2 F 20100604 20160820 20160819 20160822 EXP US-PFIZER INC-2016392856 PFIZER 53.00 YR F Y 47.00000 KG 20160822 OT 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
126688982 12668898 1 PS REVATIO SILDENAFIL CITRATE 1 Oral 40 MG, 3X/DAY 21845 40 MG FILM-COATED TABLET TID
126688982 12668898 2 C EPOPROSTENOL. EPOPROSTENOL 1 Intravenous (not otherwise specified) 67 NG/KG/MIN CONTINUOUS 0
126688982 12668898 3 C MYCOPHENOLATE MYCOPHENOLIC ACID 1 Oral 50 MG, 2X/DAY 0 50 MG BID

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126688982 12668898 1 Pulmonary hypertension
126688982 12668898 2 Pulmonary hypertension
126688982 12668898 3 Scleroderma

Outcome of event

Event ID CASEID OUTC COD
126688982 12668898 DE
126688982 12668898 HO
126688982 12668898 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
126688982 12668898 Condition aggravated
126688982 12668898 Product use issue
126688982 12668898 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
126688982 12668898 1 20100604 0
126688982 12668898 2 201207 0