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
124744833 12474483 3 F 20160618 20160628 20160617 20160701 EXP US-GILEAD-2016-0218467 GILEAD 20.00 YR A F Y 0.00000 20160701 OT 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
124744833 12474483 1 PS AMBRISENTAN AMBRISENTAN 1 Unknown 5 MG, QD 1412805A 22081 5 MG TABLET QD
124744833 12474483 2 SS REMODULIN TREPROSTINIL 1 Unknown UNK 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
124744833 12474483 1 Product used for unknown indication
124744833 12474483 2 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
124744833 12474483 OT
124744833 12474483 HO
124744833 12474483 DE

Reactions reported

Event ID CASEID DRUG REC ACT PT
124744833 12474483 Death
124744833 12474483 Headache
124744833 12474483 Nausea
124744833 12474483 Pulmonary arterial hypertension
124744833 12474483 Pulmonary oedema
124744833 12474483 Pulmonary veno-occlusive disease

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
124744833 12474483 2 20160614 0