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
125943361 12594336 1 I 20160512 20160512 20160726 20160726 EXP US-UNITED THERAPEUTICS-UNT-2016-007896 UNITED THERAPEUTICS 62.90 YR F Y 72.56000 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
125943361 12594336 1 PS REMODULIN TREPROSTINIL 1 Intravenous drip 0.062 ?G/KG, CONTINUING U U 2100909 21272 .062 UG/KG INJECTION
125943361 12594336 2 SS REMODULIN TREPROSTINIL 1 UNK U U 21272 INJECTION
125943361 12594336 3 C OPSUMIT MACITENTAN 1 0
125943361 12594336 4 C ADCIRCA TADALAFIL 1 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125943361 12594336 1 Pulmonary hypertension
125943361 12594336 3 Product used for unknown indication
125943361 12594336 4 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
125943361 12594336 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
125943361 12594336 Device related infection

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
125943361 12594336 1 20150625 0
125943361 12594336 2 20150717 0