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
120850633 12085063 3 F 20160906 20160217 20160915 EXP US-ELI_LILLY_AND_COMPANY-US201602002007 ELI LILLY AND CO 0.00 M Y 0.00000 20160914 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
120850633 12085063 1 PS ADCIRCA TADALAFIL 1 Unknown 40 MG, QD U U 21368 40 MG TABLET QD

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
120850633 12085063 1 Pulmonary arterial hypertension

Outcome of event

Event ID CASEID OUTC COD
120850633 12085063 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
120850633 12085063 Atrial flutter
120850633 12085063 Blister
120850633 12085063 Cardiac fibrillation
120850633 12085063 Dyspnoea
120850633 12085063 Herpes zoster
120850633 12085063 Peripheral swelling
120850633 12085063 Wound

Reporting Sources (this data is often not reported and may therefore be missing here)

no results found

Therapies reported

no results found