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
125941571 12594157 1 I 201512 20151215 20160726 20160726 EXP US-UNITED THERAPEUTICS-UNT-2015-015929 UNITED THERAPEUTICS 70.76 YR F Y 88.89000 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
125941571 12594157 1 PS REMODULIN TREPROSTINIL 1 Subcutaneous 0.023 ?G/KG, CONTINUING N U 926118 21272 .023 UG/KG INJECTION
125941571 12594157 2 SS ADCIRCA TADALAFIL 1 Unknown N U 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125941571 12594157 1 Pulmonary hypertension
125941571 12594157 2 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
125941571 12594157 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
125941571 12594157 Device dislocation
125941571 12594157 Drug dose omission
125941571 12594157 Flushing
125941571 12594157 Gastrointestinal disorder
125941571 12594157 Infusion site haemorrhage
125941571 12594157 Malaise
125941571 12594157 Nausea
125941571 12594157 Pain
125941571 12594157 Vomiting

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
125941571 12594157 1 20150820 0