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
125320222 12532022 2 F 20160520 20160811 20160706 20160818 EXP GB-VIIV HEALTHCARE LIMITED-GB2016093086 VIIV 51.38 YR M Y 0.00000 20160818 CN GB GB

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
125320222 12532022 1 PS ZIDOVUDINE. ZIDOVUDINE 1 Unknown 250 MG, UNK U 19655 250 MG CAPSULE
125320222 12532022 2 C COTRIMOXAZOLE SULFAMETHOXAZOLETRIMETHOPRIM 1 Oral 80/400 MG U 0 TABLET
125320222 12532022 3 C KIVEXA ABACAVIR SULFATELAMIVUDINE 1 Oral 600MG/300MG U 0 TABLET
125320222 12532022 4 C LOPINAVIR AND RITONAVIR LOPINAVIRRITONAVIR 1 Oral 200MG/50MG U 0 TABLET

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125320222 12532022 1 Product used for unknown indication
125320222 12532022 2 Product used for unknown indication
125320222 12532022 3 Product used for unknown indication
125320222 12532022 4 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
125320222 12532022 OT
125320222 12532022 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
125320222 12532022 Cerebrovascular accident

Reporting Sources (this data is often not reported and may therefore be missing here)

no results found

Therapies reported

no results found