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
127400401 12740040 1 I 20160912 20160913 20160913 EXP GB-ABBVIE-16P-167-1726033-00 ABBVIE 0.00 M Y 0.00000 20160913 OT 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
127400401 12740040 1 PS KALETRA LOPINAVIRRITONAVIR 1 Oral LOPINAVIR 400MG/5ML, RITONAVIR 100MG/5ML^ UNKNOWN 21906 100 MG TABLET
127400401 12740040 2 SS EMTRICITABINE W/TENOFOVIR EMTRICITABINETENOFOVIR DISOPROXIL 1 Oral 200MG/ 245MG UNKNOWN 0 TABLET
127400401 12740040 3 SS ONDANSETRON ONDANSETRON 1 Unknown UNKNOWN 0 8 MG
127400401 12740040 4 C SOL 2 0 60 ML

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
127400401 12740040 1 Product used for unknown indication
127400401 12740040 2 Product used for unknown indication
127400401 12740040 3 Product used for unknown indication
127400401 12740040 4 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
127400401 12740040 DE

Reactions reported

Event ID CASEID DRUG REC ACT PT
127400401 12740040 Death

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

no results found

Therapies reported

no results found