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
125500041 12550004 1 I 20160708 20160712 20160712 EXP GB-ABBVIE-16P-167-1673709-00 ABBVIE 0.00 M Y 0.00000 20160712 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
125500041 12550004 1 PS NORVIR RITONAVIR 1 Unknown UNKNOWN 22417 100 MG TABLET
125500041 12550004 2 SS TIVICAY DOLUTEGRAVIR SODIUM 1 Unknown 0 50 MG FILM-COATED TABLET
125500041 12550004 3 SS KIVEXA ABACAVIR SULFATELAMIVUDINE 1 Unknown 600/300MG 0 TABLET
125500041 12550004 4 SS ATAZANAVIR ATAZANAVIR 1 Unknown 0 300 MG CAPSULE
125500041 12550004 5 SS COTRIMOXAZOLE SULFAMETHOXAZOLETRIMETHOPRIM 1 Unknown 80/400 0 TABLET

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125500041 12550004 1 Product used for unknown indication
125500041 12550004 2 Product used for unknown indication
125500041 12550004 3 Product used for unknown indication
125500041 12550004 4 Product used for unknown indication
125500041 12550004 5 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
125500041 12550004 DE

Reactions reported

Event ID CASEID DRUG REC ACT PT
125500041 12550004 Death

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

no results found

Therapies reported

no results found