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
125796381 12579638 1 I 20160630 20160713 20160721 20160721 EXP US-ELI_LILLY_AND_COMPANY-US201607005061 ELI LILLY AND CO 12.00 YR F Y 0.00000 20160721 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
125796381 12579638 1 PS ADCIRCA TADALAFIL 1 Unknown UNK, UNKNOWN U U 21368 TABLET
125796381 12579638 2 SS AMBRISENTAN AMBRISENTAN 1 Unknown 10 MG, QD 0 10 MG QD
125796381 12579638 3 SS REMODULIN TREPROSTINIL 1 Unknown UNK, UNKNOWN U U 0
125796381 12579638 4 C PRILOSEC OMEPRAZOLE MAGNESIUM 1 0
125796381 12579638 5 C STRATTERA ATOMOXETINE HYDROCHLORIDE 1 0
125796381 12579638 6 C ZYRTEC CETIRIZINE HYDROCHLORIDE 1 0
125796381 12579638 7 C LASIX FUROSEMIDE 1 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125796381 12579638 1 Product used for unknown indication
125796381 12579638 2 Pulmonary hypertension
125796381 12579638 3 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
125796381 12579638 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
125796381 12579638 Clostridium difficile infection
125796381 12579638 Myalgia
125796381 12579638 Off label use
125796381 12579638 Pain

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
125796381 12579638 2 20120802 0