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
124162224 12416222 4 F 20160811 20160530 20160812 EXP US-GILEAD-2016-0215365 GILEAD 24.00 YR A F Y 0.00000 20160812 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
124162224 12416222 1 PS AMBRISENTAN AMBRISENTAN 1 Unknown 5 MG, QD 1413104A 22081 5 MG TABLET QD
124162224 12416222 2 SS REMODULIN TREPROSTINIL 1 Unknown UNK U 0
124162224 12416222 3 C COUMADIN WARFARIN SODIUM 1 0
124162224 12416222 4 C ADCIRCA TADALAFIL 1 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
124162224 12416222 1 Pulmonary arterial hypertension
124162224 12416222 2 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
124162224 12416222 OT
124162224 12416222 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
124162224 12416222 Administration site hyperaesthesia
124162224 12416222 Administration site pruritus
124162224 12416222 Catheterisation cardiac
124162224 12416222 Infusion site abscess
124162224 12416222 Infusion site pain

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
124162224 12416222 2 20160517 20160519 0