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
125592341 12559234 1 I 20160620 20160627 20160715 20160715 PER US-ELI_LILLY_AND_COMPANY-US201606009356 ELI LILLY AND CO 56.00 YR M Y 0.00000 20160715 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
125592341 12559234 1 PS ADCIRCA TADALAFIL 1 Unknown UNK UNK, UNKNOWN U U 21368 TABLET
125592341 12559234 2 SS AMBRISENTAN AMBRISENTAN 1 Unknown UNK, UNKNOWN 0
125592341 12559234 3 SS AMBRISENTAN AMBRISENTAN 1 Unknown 10 MG, QD 1504768A 0 10 MG QD
125592341 12559234 4 SS TYVASO TREPROSTINIL 1 Unknown UNK, UNKNOWN U U 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125592341 12559234 1 Product used for unknown indication
125592341 12559234 2 Pulmonary hypertension
125592341 12559234 4 Product used for unknown indication

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
125592341 12559234 Balance disorder
125592341 12559234 Dizziness
125592341 12559234 Gait disturbance

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
125592341 12559234 3 20160607 0