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
125002902 12500290 2 F 20160725 20160627 20160801 EXP US-ELI_LILLY_AND_COMPANY-US201606005504 ELI LILLY AND CO 0.00 F Y 0.00000 20160801 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
125002902 12500290 1 PS ADCIRCA TADALAFIL 1 Unknown 20 MG, BID U U 21368 20 MG TABLET BID
125002902 12500290 2 I LETAIRIS AMBRISENTAN 1 Unknown 10 MG, QD 1504768A 0 10 MG QD

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125002902 12500290 1 Product used for unknown indication
125002902 12500290 2 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
125002902 12500290 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
125002902 12500290 Bone pain
125002902 12500290 Chest discomfort
125002902 12500290 Chills
125002902 12500290 Cough
125002902 12500290 Dyspnoea
125002902 12500290 Eye swelling
125002902 12500290 Headache
125002902 12500290 Pain in extremity
125002902 12500290 Peripheral swelling
125002902 12500290 Pulmonary mass
125002902 12500290 Rheumatoid arthritis
125002902 12500290 Tremor
125002902 12500290 Upper-airway cough syndrome

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
125002902 12500290 1 201605 0
125002902 12500290 2 201605 0