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
125377471 12537747 1 I 20120802 20160705 20160707 20160707 EXP US-GILEAD-2016-0222443 GILEAD 12.00 YR T F Y 0.00000 20160707 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
125377471 12537747 1 PS AMBRISENTAN AMBRISENTAN 1 Unknown 10 MG, QD 1509427A 22081 10 MG TABLET QD
125377471 12537747 2 SS ADCIRCA TADALAFIL 1 Unknown U 0
125377471 12537747 3 SS REMODULIN TREPROSTINIL 1 Unknown U 0
125377471 12537747 4 C PRILOSEC OMEPRAZOLE MAGNESIUM 1 0
125377471 12537747 5 C STRATTERA ATOMOXETINE HYDROCHLORIDE 1 0
125377471 12537747 6 C ZYRTEC CETIRIZINE HYDROCHLORIDE 1 0
125377471 12537747 7 C LASIX FUROSEMIDE 1 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125377471 12537747 1 Pulmonary hypertension
125377471 12537747 2 Product used for unknown indication
125377471 12537747 3 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
125377471 12537747 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
125377471 12537747 Clostridium difficile infection
125377471 12537747 Myalgia
125377471 12537747 Off label use
125377471 12537747 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
125377471 12537747 1 20120802 0