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
124302052 12430205 2 F 20160406 20160907 20160602 20160915 EXP PT-INFARMED-S201605-89 PT-VIIV HEALTHCARE LIMITED-PT2016077212 VIIV 44.17 YR M Y 0.00000 20160915 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
124302052 12430205 1 PS COMBIVIR LAMIVUDINEIDOVUDINE 1 Oral 1 DF, QD 2812 DF 20857 1 DF FILM-COATED TABLET QD
124302052 12430205 2 SS KALETRA LOPINAVIRRITONAVIR 1 Oral 1 DF, QD 2812 DF 0 1 DF FILM-COATED TABLET QD
124302052 12430205 3 SS HARVONI LEDIPASVIRSOFOSBUVIR 1 Oral 1 DF, QD 0 1 DF FILM-COATED TABLET QD

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
124302052 12430205 1 HIV infection
124302052 12430205 2 HIV infection
124302052 12430205 3 Chronic hepatitis C

Outcome of event

Event ID CASEID OUTC COD
124302052 12430205 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
124302052 12430205 Ascites
124302052 12430205 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
124302052 12430205 1 20080725 20160406 0
124302052 12430205 2 20080725 20160406 0
124302052 12430205 3 201506 201512 0