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
125737401 12573740 1 I 20160703 20160714 20160720 20160720 PER US-ELI_LILLY_AND_COMPANY-US201607005538 ELI LILLY AND CO 57.00 YR F Y 0.00000 20160720 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
125737401 12573740 1 PS ADCIRCA TADALAFIL 1 Unknown UNK, UNKNOWN 21368 TABLET
125737401 12573740 2 SS LETAIRIS AMBRISENTAN 1 Unknown 5 MG, QD 1413104A 0 5 MG QD

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125737401 12573740 1 Product used for unknown indication
125737401 12573740 2 Product used for unknown indication

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
125737401 12573740 Headache
125737401 12573740 Intervertebral disc protrusion
125737401 12573740 Nasal oedema
125737401 12573740 Oedema peripheral
125737401 12573740 Palpitations
125737401 12573740 Procedural hypotension
125737401 12573740 Spider vein

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
125737401 12573740 1 20160703 0
125737401 12573740 2 20160630 0