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
125309132 12530913 2 F 20160627 20160713 20160706 20160720 EXP US-UNITED THERAPEUTICS-UNT-2016-010443 UNITED THERAPEUTICS 28.67 YR F Y 61.68000 KG 20160720 OT 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
125309132 12530913 1 PS REMODULIN TREPROSTINIL 1 Subcutaneous 0.020 ?G/KG, CONTINUING U U 2100955 21272 .02 UG/KG INJECTION
125309132 12530913 2 C ADCIRCA TADALAFIL 1 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125309132 12530913 1 Pulmonary arterial hypertension
125309132 12530913 2 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
125309132 12530913 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
125309132 12530913 Device issue
125309132 12530913 Dizziness
125309132 12530913 Drug dose omission
125309132 12530913 Dyspnoea
125309132 12530913 Infusion site erythema
125309132 12530913 Infusion site induration
125309132 12530913 Infusion site oedema
125309132 12530913 Infusion site pustule
125309132 12530913 Palpitations
125309132 12530913 Presyncope
125309132 12530913 Stress

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
125309132 12530913 1 20160404 0