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
127278631 12727863 1 I 20160830 20160909 20160909 EXP FR-ACTELION-A-CH2016-141800 ACTELION 15.00 YR T M Y 0.00000 20160909 MD FR FR

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
127278631 12727863 1 PS VELETRI EPOPROSTENOL 1 Intravenous (not otherwise specified) UNK 22260 INJECTION
127278631 12727863 2 SS TRACLEER BOSENTAN 1 Oral UNK 21290 TABLET
127278631 12727863 3 C REVATIO SILDENAFIL CITRATE 1 U 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
127278631 12727863 1 Pulmonary arterial hypertension
127278631 12727863 2 Pulmonary arterial hypertension

Outcome of event

Event ID CASEID OUTC COD
127278631 12727863 HO
127278631 12727863 OT
127278631 12727863 DE

Reactions reported

Event ID CASEID DRUG REC ACT PT
127278631 12727863 Condition aggravated
127278631 12727863 Lung disorder
127278631 12727863 Pulmonary arterial 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
127278631 12727863 1 2016 2016 0
127278631 12727863 2 2016 20160815 0