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
125379862 12537986 2 F 201601 20160919 20160707 20160923 EXP GB-ABBVIE-16P-167-1669163-00 ABBVIE 44.00 YR M Y 0.00000 20160923 MD 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
125379862 12537986 1 PS NORVIR RITONAVIR 1 Oral Y UNKNOWN 20945 SOFT CAPSULE
125379862 12537986 2 SS DARUNAVIR DARUNAVIR 1 Oral Y UNKNOWN 0 TABLET
125379862 12537986 3 SS KIVEXA ABACAVIR SULFATELAMIVUDINE 1 Oral Y UNKNOWN 0
125379862 12537986 4 SS TRIUMEQ ABACAVIR SULFATEDOLUTEGRAVIR SODIUMLAMIVUDINE 1 Oral Y UNKNOWN 0 QD

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125379862 12537986 1 Product used for unknown indication
125379862 12537986 2 Product used for unknown indication
125379862 12537986 3 Product used for unknown indication
125379862 12537986 4 HIV infection

Outcome of event

Event ID CASEID OUTC COD
125379862 12537986 HO
125379862 12537986 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
125379862 12537986 Coronary artery disease
125379862 12537986 Malabsorption
125379862 12537986 Skin lesion
125379862 12537986 Subcutaneous abscess
125379862 12537986 Treatment failure
125379862 12537986 Viral load increased
125379862 12537986 Viral mutation identified
125379862 12537986 Weight increased

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
125379862 12537986 1 20151224 0
125379862 12537986 2 20151224 0
125379862 12537986 3 20151224 0
125379862 12537986 4 20151230 20160412 0