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
126747371 12674737 1 I 20140803 20160816 20160822 20160822 EXP US-ELI_LILLY_AND_COMPANY-US201608008810 ELI LILLY AND CO 77.00 YR F Y 0.00000 20160819 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
126747371 12674737 1 PS ADCIRCA TADALAFIL 1 Unknown UNK, UNKNOWN Y U 21368 TABLET
126747371 12674737 2 SS LETAIRIS AMBRISENTAN 1 Unknown 5 MG, QD Y U 1413180A 0 5 MG QD
126747371 12674737 3 SS LETAIRIS AMBRISENTAN 1 Unknown 2.5 MG, QD Y U 0 2.5 MG QD

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126747371 12674737 1 Product used for unknown indication
126747371 12674737 2 Pulmonary hypertension

Outcome of event

Event ID CASEID OUTC COD
126747371 12674737 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
126747371 12674737 Dyspnoea
126747371 12674737 Eye swelling
126747371 12674737 Flushing
126747371 12674737 Heart rate increased
126747371 12674737 Oedema

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
126747371 12674737 2 20160714 0