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
125243231 12524323 1 I 201605 20160531 20160704 20160704 EXP US-UNITED THERAPEUTICS-UNT-2016-008907 UNITED THERAPEUTICS 68.14 YR F Y 81.63000 KG 20160704 CN 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
125243231 12524323 1 PS TYVASO TREPROSTINIL 1 54-72 MICROGRAMS, QID 2100765 22387 INHALATION GAS QID
125243231 12524323 2 C LETAIRIS AMBRISENTAN 1 0
125243231 12524323 3 C ADCIRCA TADALAFIL 1 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125243231 12524323 1 Pulmonary hypertension
125243231 12524323 2 Product used for unknown indication
125243231 12524323 3 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
125243231 12524323 DE

Reactions reported

Event ID CASEID DRUG REC ACT PT
125243231 12524323 Death
125243231 12524323 General physical health deterioration
125243231 12524323 Product use issue

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
125243231 12524323 1 20120801 0