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
124335023 12433502 3 F 20160715 20160603 20160719 PER US-ELI_LILLY_AND_COMPANY-US201605005228 ELI LILLY AND CO 61.00 YR F Y 65.31000 KG 20160719 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
124335023 12433502 1 PS ADCIRCA TADALAFIL 1 Unknown UNK, UNKNOWN U U 21368 TABLET
124335023 12433502 2 SS AMBRISENTAN AMBRISENTAN 1 Unknown 5 MG, QD U U 1412805A 0 5 MG QD
124335023 12433502 3 C WARFARIN WARFARIN 1 0
124335023 12433502 4 C SILDENAFIL. SILDENAFIL 1 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
124335023 12433502 1 Product used for unknown indication
124335023 12433502 2 Pulmonary hypertension

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
124335023 12433502 Abdominal pain upper
124335023 12433502 Back pain
124335023 12433502 Drug intolerance
124335023 12433502 Headache
124335023 12433502 Insomnia
124335023 12433502 Pain
124335023 12433502 Pain in extremity
124335023 12433502 Presyncope

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
124335023 12433502 2 20160421 0