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
125759281 12575928 1 I 20160422 20160714 20160720 20160720 PER US-ELI_LILLY_AND_COMPANY-US201607005558 ELI LILLY AND CO 48.00 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
125759281 12575928 1 PS ADCIRCA TADALAFIL 1 Unknown UNK, UNKNOWN U U 21368 TABLET
125759281 12575928 2 SS LETAIRIS AMBRISENTAN 1 Unknown 10 MG, QD U U 1504768A 0 10 MG QD

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125759281 12575928 1 Product used for unknown indication
125759281 12575928 2 Product used for unknown indication

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
125759281 12575928 Allergic cough
125759281 12575928 Arthralgia
125759281 12575928 Chest pain
125759281 12575928 Headache
125759281 12575928 Myalgia
125759281 12575928 Nasal congestion
125759281 12575928 Seasonal allergy
125759281 12575928 Tinnitus
125759281 12575928 Vomiting

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
125759281 12575928 2 20140918 0