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
124864922 12486492 2 F 20160604 20160629 20160621 20160706 EXP US-ABBVIE-16P-163-1652041-00 ABBVIE 48.08 YR M Y 0.00000 20160706 CN COUNTRY NOT SPECIFIED 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
124864922 12486492 1 PS VIEKIRA PAK DASABUVIROMBITASVIRPARITAPREVIRRITONAVIR 1 Oral 1052006 206619 TABLET
124864922 12486492 2 SS RIBAVIRIN. RIBAVIRIN 1 Oral Y AED7284Z 0 600 MG TABLET BID
124864922 12486492 3 SS RIBAVIRIN. RIBAVIRIN 1 Oral Y AED7284Z 0 200 MG TABLET TID

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
124864922 12486492 1 Hepatitis C
124864922 12486492 2 Hepatitis C

Outcome of event

Event ID CASEID OUTC COD
124864922 12486492 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
124864922 12486492 Anaemia
124864922 12486492 Decreased appetite
124864922 12486492 Dehydration
124864922 12486492 Fatigue
124864922 12486492 Influenza like illness

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
124864922 12486492 1 20160428 0
124864922 12486492 2 20160428 20160606 0
124864922 12486492 3 20160607 0