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
116589673 11658967 3 F 20160727 20160808 20151026 20160812 EXP TW-ACTELION-A-CH2015-126129 ACTELION 65.00 YR E F Y 0.00000 20160812 CN TW TW

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
116589673 11658967 1 PS OPSUMIT MACITENTAN 1 Oral 10 MG, OD 204410 10 MG TABLET QD
116589673 11658967 2 SS REVATIO SILDENAFIL CITRATE 1 Oral 20 MG, TID 0 20 MG TID
116589673 11658967 3 C SECORIN 2 10 MG, BID U 0 10 MG BID

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
116589673 11658967 1 Pulmonary arterial hypertension
116589673 11658967 2 Pulmonary arterial hypertension

Outcome of event

Event ID CASEID OUTC COD
116589673 11658967 OT
116589673 11658967 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
116589673 11658967 Back pain
116589673 11658967 Lung cancer metastatic
116589673 11658967 Metastases to bone
116589673 11658967 Pain in extremity

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
116589673 11658967 1 20150408 0
116589673 11658967 2 201503 0
116589673 11658967 3 201502 0