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
124929362 12492936 2 F 201605 20160624 20160623 20160706 EXP US-ACTELION-A-US2016-136674 ACTELION 73.00 YR E F Y 0.00000 20160706 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
124929362 12492936 1 PS TRACLEER BOSENTAN 1 Oral 62.5 MG, BID NP013P0402 21290 62.5 MG TABLET BID
124929362 12492936 2 C AMLODIPINE AMLODIPINE BESYLATE 1 10 MG, UNK U 0 10 MG
124929362 12492936 3 C OXYGEN. OXYGEN 1 U 0
124929362 12492936 4 C FUROSEMIDE. FUROSEMIDE 1 20 MG, UNK U 0 20 MG QD
124929362 12492936 5 C MINOXIDIL. MINOXIDIL 1 2.5 MG, UNK U 0 2.5 MG QD
124929362 12492936 6 C CLONIDINE. CLONIDINE 1 0.1 MG, BID U 0 .1 MG BID
124929362 12492936 7 C VALSARTAN AND HYDROCHLOROTHIAZIDE HYDROCHLOROTHIAZIDEVALSARTAN 1 U 0 QD

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
124929362 12492936 1 Pulmonary arterial hypertension

Outcome of event

Event ID CASEID OUTC COD
124929362 12492936 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
124929362 12492936 Cardiomegaly
124929362 12492936 Chest pain
124929362 12492936 Hypertension
124929362 12492936 Peripheral swelling
124929362 12492936 Venous operation

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
124929362 12492936 1 20130715 0