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
125911552 12591155 2 F 201603 20160329 20160726 20160727 PER US-UNITED THERAPEUTICS-UNT-2016-004070 UNITED THERAPEUTICS 1.64 YR M Y 8.62000 KG 20160727 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
125911552 12591155 1 PS REMODULIN TREPROSTINIL 1 Subcutaneous 0.022 ?G/KG, CONTINUING U U 2100579 21272 .022 UG/KG INJECTION
125911552 12591155 2 SS REMODULIN TREPROSTINIL 1 Subcutaneous 0.047 ?G/KG, CONTINUING U U 21272 .047 UG/KG INJECTION
125911552 12591155 3 C SILDENAFIL. SILDENAFIL 1 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125911552 12591155 1 Pulmonary hypertension
125911552 12591155 3 Product used for unknown indication

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
125911552 12591155 Dermatitis contact
125911552 12591155 Infusion site injury
125911552 12591155 Infusion site nodule
125911552 12591155 Thrombosis in device

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
125911552 12591155 1 20150403 0