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
125940941 12594094 1 I 2015 20151223 20160726 20160726 EXP US-UNITED THERAPEUTICS-UNT-2015-016395 UNITED THERAPEUTICS 31.07 YR F Y 66.67000 KG 20160726 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
125940941 12594094 1 PS TYVASO TREPROSTINIL 1 18-54 ?G, QID U U 2100705 22387 INHALATION GAS QID
125940941 12594094 2 SS TYVASO TREPROSTINIL 1 6 SESSION/DAY U U 22387 INHALATION GAS
125940941 12594094 3 SS LETAIRIS AMBRISENTAN 1 Unknown 10 MG, QD SBFX 0 10 MG TABLET QD
125940941 12594094 4 SS ADCIRCA TADALAFIL 1 Unknown UNK U U 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125940941 12594094 1 Pulmonary hypertension
125940941 12594094 3 Product used for unknown indication
125940941 12594094 4 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
125940941 12594094 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
125940941 12594094 Fall
125940941 12594094 Hypotension
125940941 12594094 Inappropriate schedule of drug administration
125940941 12594094 Syncope

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
125940941 12594094 1 20150303 0
125940941 12594094 3 20150313 0