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
125367542 12536754 2 F 201606 20160809 20160707 20160816 EXP US-UNITED THERAPEUTICS-UNT-2016-010691 UNITED THERAPEUTICS 44.41 YR M Y 102.40000 KG 20160816 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
125367542 12536754 1 PS REMODULIN TREPROSTINIL 1 Intravenous drip 0.025 ?G/KG, CONTINUING U U 2100955 21272 .025 UG/KG INJECTION
125367542 12536754 2 SS REMODULIN TREPROSTINIL 1 Intravenous drip 0.022 ?G/KG, CONTINUING U U 929005 21272 .022 UG/KG INJECTION
125367542 12536754 3 C LETAIRIS AMBRISENTAN 1 0
125367542 12536754 4 C ADCIRCA TADALAFIL 1 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125367542 12536754 1 Pulmonary arterial hypertension
125367542 12536754 3 Product used for unknown indication
125367542 12536754 4 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
125367542 12536754 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
125367542 12536754 Biopsy lung
125367542 12536754 Cardiac failure
125367542 12536754 Dermatitis contact

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
125367542 12536754 1 20160203 0