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
124336993 12433699 3 F 20160406 20160907 20160603 20160914 EXP PT-INFARMED-S201605-89 PT-GILEAD-2016-0216454 GILEAD 44.00 YR A M Y 0.00000 20160914 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
124336993 12433699 1 PS HARVONI LEDIPASVIRSOFOSBUVIR 1 Oral 1 DF, QD 205834 1 DF TABLET QD
124336993 12433699 2 SS KALETRA LOPINAVIRRITONAVIR 1 Oral 1 DF, QD 2812 DF 0 1 DF QD
124336993 12433699 3 SS COMBIVIR LAMIVUDINEIDOVUDINE 1 Oral 1 DF, QD 2812 DF 0 1 DF QD

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
124336993 12433699 1 Chronic hepatitis C
124336993 12433699 2 HIV infection
124336993 12433699 3 HIV infection

Outcome of event

Event ID CASEID OUTC COD
124336993 12433699 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
124336993 12433699 Ascites
124336993 12433699 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
124336993 12433699 1 201506 201512 0
124336993 12433699 2 20080725 20160406 0
124336993 12433699 3 20080725 20160406 0