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
125503091 12550309 1 I 20160217 20160707 20160712 20160712 EXP FR-ABBVIE-16P-056-1671764-00 ABBVIE 51.96 YR F Y 0.00000 20160712 MD FR FR

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
125503091 12550309 1 PS NORVIR RITONAVIR 1 Oral UNKNOWN 22417 100 MG TABLET QD
125503091 12550309 2 SS DOCETAXEL HOSPIRA DOCETAXEL 1 Intravenous (not otherwise specified) 100MG/M2 0
125503091 12550309 3 SS REYATAZ ATAZANAVIR SULFATE 1 Oral 0 CAPSULE QD

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125503091 12550309 1 HIV infection
125503091 12550309 2 Invasive ductal breast carcinoma
125503091 12550309 3 HIV infection

Outcome of event

Event ID CASEID OUTC COD
125503091 12550309 HO
125503091 12550309 DE
125503091 12550309 LT

Reactions reported

Event ID CASEID DRUG REC ACT PT
125503091 12550309 Atelectasis
125503091 12550309 Cardio-respiratory arrest
125503091 12550309 Generalised oedema
125503091 12550309 Multiple organ dysfunction syndrome
125503091 12550309 Neutropenic colitis
125503091 12550309 Pancytopenia
125503091 12550309 Septic shock
125503091 12550309 Stomatitis
125503091 12550309 Toxic skin eruption

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
125503091 12550309 1 20160305 0
125503091 12550309 2 20160212 20160212 0
125503091 12550309 3 20160305 0