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
124790464 12479046 4 F 20160906 20160620 20160914 PER US-ELI_LILLY_AND_COMPANY-US201606005399 ELI LILLY AND CO 73.00 YR F Y 41.27000 KG 20160914 MD 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
124790464 12479046 1 PS ADCIRCA TADALAFIL 1 Unknown UNK, UNKNOWN Y N 21368 TABLET
124790464 12479046 2 SS AMBRISENTAN AMBRISENTAN 1 Unknown 5 MG, QD Y 1504767A 0 5 MG QD
124790464 12479046 3 SS AMBRISENTAN AMBRISENTAN 1 Unknown 10 MG, QD Y 1509507A 0 10 MG QD

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
124790464 12479046 1 Product used for unknown indication
124790464 12479046 2 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
124790464 12479046 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
124790464 12479046 Deafness
124790464 12479046 Ear congestion
124790464 12479046 Middle ear effusion
124790464 12479046 Musculoskeletal pain
124790464 12479046 Neck pain
124790464 12479046 Neuralgia
124790464 12479046 Pain

Reporting Sources (this data is often not reported and may therefore be missing here)

no results found

Therapies reported

no results found