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
124399382 12439938 2 F 20160406 20160907 20160606 20160912 EXP PT-ABBVIE-16K-130-1643094-00 ABBVIE 44.17 YR M Y 0.00000 20160912 PH PT PT

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
124399382 12439938 1 PS KALETRA LOPINAVIRRITONAVIR 1 Oral 200MG + 50MG UNKNOWN 21906 FILM-COATED TABLET QD
124399382 12439938 2 SS COMBIVIR LAMIVUDINEIDOVUDINE 1 Oral 150MG + 300MG 0 FILM-COATED TABLET QD
124399382 12439938 3 SS HARVONI LEDIPASVIRSOFOSBUVIR 1 Oral 90MG + 400MG 0 FILM-COATED TABLET QD

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
124399382 12439938 1 HIV infection
124399382 12439938 2 HIV infection
124399382 12439938 3 Chronic hepatitis C

Outcome of event

Event ID CASEID OUTC COD
124399382 12439938 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
124399382 12439938 Ascites
124399382 12439938 Hepatic enzyme abnormal

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
124399382 12439938 1 20080725 20160406 0
124399382 12439938 2 20080725 20160406 0
124399382 12439938 3 201506 201512 0