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
124493303 12449330 3 F 20160711 20160608 20160719 EXP US-ELI_LILLY_AND_COMPANY-US201605009931 ELI LILLY AND CO 25.00 YR F Y 0.00000 20160718 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
124493303 12449330 1 PS ADCIRCA TADALAFIL 1 Unknown 40 MG, UNKNOWN U U 21368 40 MG TABLET
124493303 12449330 2 SS AMBRISENTAN AMBRISENTAN 1 Oral 5 MG, QD 1500227A 0 5 MG QD
124493303 12449330 3 SS AMBRISENTAN AMBRISENTAN 1 Oral 10 MG, QD 1500227A 0 10 MG QD
124493303 12449330 4 C SIMVASTATIN. SIMVASTATIN 1 0
124493303 12449330 5 C NOVOLOG INSULIN ASPART 1 0
124493303 12449330 6 C FUROSEMIDE. FUROSEMIDE 1 0
124493303 12449330 7 C LEVEMIR INSULIN DETEMIR 1 0
124493303 12449330 8 C HYDRALAZINE HYDRALAZINE HYDROCHLORIDE 1 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
124493303 12449330 1 Product used for unknown indication
124493303 12449330 2 Pulmonary hypertension

Outcome of event

Event ID CASEID OUTC COD
124493303 12449330 OT
124493303 12449330 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
124493303 12449330 End stage renal disease
124493303 12449330 Pneumonia
124493303 12449330 Pulmonary arterial hypertension
124493303 12449330 Sepsis

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
124493303 12449330 2 20150914 20160217 0
124493303 12449330 3 20160218 0