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
125731861 12573186 1 I 20160703 20160706 20160720 20160720 PER US-ELI_LILLY_AND_COMPANY-US201607002574 ELI LILLY AND CO 65.00 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
125731861 12573186 1 PS ADCIRCA TADALAFIL 1 Oral 20 MG, DAILY N U C495978A 21368 20 MG TABLET QD
125731861 12573186 2 C METFORMIN METFORMIN HYDROCHLORIDE 1 0
125731861 12573186 3 C POTASSIUM POTASSIUM 1 0
125731861 12573186 4 C OXYGEN. OXYGEN 1 UNK, EACH EVENING 0 QD

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125731861 12573186 1 Pulmonary hypertension

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
125731861 12573186 Abdominal discomfort
125731861 12573186 Arthralgia
125731861 12573186 Back pain
125731861 12573186 Feeling abnormal
125731861 12573186 Groin pain
125731861 12573186 Insomnia
125731861 12573186 Pain in extremity
125731861 12573186 Pelvic pain
125731861 12573186 Rash pruritic

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
125731861 12573186 1 20160702 20160703 0