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
125910712 12591071 2 F 201512 20160125 20160726 20160726 PER US-UNITED THERAPEUTICS-UNT-2015-015670 UNITED THERAPEUTICS 52.59 YR F Y 56.69000 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
125910712 12591071 1 PS REMODULIN TREPROSTINIL 1 Subcutaneous 0.185 ?G/KG/MIN, CONTINUING U U 2100665 21272 .185 UG/KG INJECTION
125910712 12591071 2 SS LETAIRIS AMBRISENTAN 1 10 MG, QD SBFX 0 10 MG QD
125910712 12591071 3 SS LETAIRIS AMBRISENTAN 1 UNK 1500226A 0
125910712 12591071 4 C REVATIO SILDENAFIL CITRATE 1 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125910712 12591071 1 Pulmonary arterial hypertension
125910712 12591071 2 Scleroderma
125910712 12591071 4 Product used for unknown indication

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
125910712 12591071 Arthralgia
125910712 12591071 Oedema peripheral
125910712 12591071 Pain in extremity

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
125910712 12591071 1 20090616 0
125910712 12591071 2 20150617 0