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
124972923 12497292 3 F 20160919 20160624 20160920 EXP US-BAYER-2016-047476 BAYER 72.00 YR E F Y 112.00000 KG 20160920 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
124972923 12497292 1 PS ADEMPAS RIOCIGUAT 1 Oral UNK 204819
124972923 12497292 2 SS ADEMPAS RIOCIGUAT 1 Oral 2 MG, TID BXH6TG1 204819 2 MG TID
124972923 12497292 3 SS ADEMPAS RIOCIGUAT 1 Oral 2.5 MG, UNK BXH8FC1 204819 2.5 MG
124972923 12497292 4 SS ADEMPAS RIOCIGUAT 1 Oral 2.5 MG, TID BXH8FC2 204819 2.5 MG TID
124972923 12497292 5 SS LETAIRIS AMBRISENTAN 1 Unknown 5 MG, QD SBFP 0 5 MG QD
124972923 12497292 6 C OXYGEN. OXYGEN 1 UNK 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
124972923 12497292 1 Pulmonary arterial hypertension
124972923 12497292 2 Pulmonary arterial hypertension
124972923 12497292 3 Pulmonary arterial hypertension
124972923 12497292 4 Pulmonary arterial hypertension

Outcome of event

Event ID CASEID OUTC COD
124972923 12497292 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
124972923 12497292 Adverse event
124972923 12497292 Dry mouth
124972923 12497292 Dry skin
124972923 12497292 Dyspnoea
124972923 12497292 Joint swelling
124972923 12497292 Oedema peripheral
124972923 12497292 Pruritus
124972923 12497292 Pulmonary thrombosis
124972923 12497292 Rash

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
124972923 12497292 1 20151016 0
124972923 12497292 5 20150610 0