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
124023623 12402362 3 F 20120802 20160608 20160525 20160715 EXP US-GILEAD-2016-0215490 GILEAD 12.00 YR T F Y 0.00000 20160715 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
124023623 12402362 1 PS AMBRISENTAN AMBRISENTAN 1 Unknown 10 MG, QD 1503901A 22081 10 MG TABLET QD
124023623 12402362 2 SS REMODULIN TREPROSTINIL 1 Unknown 91 NG, Q1MINUTE U 2100909 0 91 NG /min

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
124023623 12402362 1 Pulmonary hypertension
124023623 12402362 2 Pulmonary hypertension

Outcome of event

Event ID CASEID OUTC COD
124023623 12402362 HO
124023623 12402362 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
124023623 12402362 Catheter placement
124023623 12402362 Device related infection
124023623 12402362 Off label use

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
124023623 12402362 1 20120802 0
124023623 12402362 2 20151216 0