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
125918081 12591808 1 I 201602 20160215 20160726 20160726 PER US-UNITED THERAPEUTICS-UNT-2016-002401 UNITED THERAPEUTICS 52.38 YR M Y 136.50000 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
125918081 12591808 1 PS ORENITRAM TREPROSTINIL 1 Oral 2.25 MG, TID U U 2100397 203496 2.25 MG TABLET TID
125918081 12591808 2 SS ORENITRAM TREPROSTINIL 1 Oral UNK U U 2100477 203496 TABLET
125918081 12591808 3 SS REVATIO SILDENAFIL CITRATE 1 Unknown U U 0
125918081 12591808 4 SS LETAIRIS AMBRISENTAN 1 Oral 10 MG, QD 1500225A 0 10 MG TABLET QD

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125918081 12591808 1 Pulmonary hypertension
125918081 12591808 3 Product used for unknown indication
125918081 12591808 4 Product used for unknown indication

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
125918081 12591808 Flushing
125918081 12591808 Headache
125918081 12591808 Hyperhidrosis
125918081 12591808 Malaise

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
125918081 12591808 1 20150508 0
125918081 12591808 4 20100126 0