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
125814141 12581414 1 I 20160718 20160721 20160721 EXP IT-ABBVIE-16P-083-1682659-00 ABBVIE 54.00 YR F Y 0.00000 20160721 MD IT IT

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
125814141 12581414 1 PS NORVIR RITONAVIR 1 Unknown UNKNOWN 20945
125814141 12581414 2 SS PREZISTA DARUNAVIR ETHANOLATE 1 Unknown UNKNOWN 0
125814141 12581414 3 SS TRUVADA EMTRICITABINETENOFOVIR DISOPROXIL FUMARATE 1 Unknown UNKNOWN 0 COATED TABLET
125814141 12581414 4 C RALTEGRAVIR. RALTEGRAVIR 1 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125814141 12581414 1 Product used for unknown indication
125814141 12581414 2 Product used for unknown indication
125814141 12581414 3 Product used for unknown indication
125814141 12581414 4 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
125814141 12581414 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
125814141 12581414 Chronic kidney disease

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

no results found

Therapies reported

no results found