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
119428302 11942830 2 F 201507 20160201 20160125 20160726 PER US-UNITED THERAPEUTICS-UNT-2015-008917 UNITED THERAPEUTICS 83.74 YR F Y 95.24000 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
119428302 11942830 1 PS REMODULIN TREPROSTINIL 1 Intravenous drip 0.084 ?G/KG/MIN, CONTINUING U U 2100664 21272 .084 UG/KG INJECTION
119428302 11942830 2 SS REMODULIN TREPROSTINIL 1 Intravenous drip 0.335 ?G/KG/MIN, CONTINUING U U 21272 .335 UG/KG INJECTION
119428302 11942830 3 SS REMODULIN TREPROSTINIL 1 UNK U U 2100582 21272 INJECTION
119428302 11942830 4 SS REMODULIN TREPROSTINIL 1 UNK U U 2100666 21272 INJECTION
119428302 11942830 5 C REVATIO SILDENAFIL CITRATE 1 0
119428302 11942830 6 C TRACLEER BOSENTAN 1 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
119428302 11942830 1 Pulmonary arterial hypertension
119428302 11942830 5 Product used for unknown indication
119428302 11942830 6 Product used for unknown indication

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
119428302 11942830 Bile duct stenosis
119428302 11942830 Fatigue
119428302 11942830 Headache
119428302 11942830 Herpes zoster
119428302 11942830 Post herpetic neuralgia
119428302 11942830 Weight decreased

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
119428302 11942830 1 20150324 0
119428302 11942830 2 20150324 0