The Safety Rates Drug Report

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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
125909622 12590962 2 F 201511 20160122 20160726 20160726 PER US-UNITED THERAPEUTICS-UNT-2015-015240 UNITED THERAPEUTICS 71.70 YR F Y 51.70000 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
125909622 12590962 1 PS REMODULIN TREPROSTINIL 1 Subcutaneous 0.049 ?G/KG, CONTINUING U U 924715 21272 .049 UG/KG INJECTION
125909622 12590962 2 SS REMODULIN TREPROSTINIL 1 UNK U U 926118 21272 INJECTION
125909622 12590962 3 SS LETAIRIS AMBRISENTAN 1 Unknown 5 MG, QD 1403838A 0 5 MG TABLET QD
125909622 12590962 4 C ADCIRCA TADALAFIL 1 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125909622 12590962 1 Pulmonary hypertension
125909622 12590962 2 Systemic scleroderma
125909622 12590962 3 Product used for unknown indication
125909622 12590962 4 Product used for unknown indication

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
125909622 12590962 Infusion site discharge
125909622 12590962 Infusion site erythema
125909622 12590962 Infusion site infection

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
125909622 12590962 1 20131219 0
125909622 12590962 3 20140206 0