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
125575512 12557551 2 F 20160712 20160714 20160722 EXP AT-JNJFOC-20160706653 JANSSEN 0.00 F Y 0.00000 20160722 CN US AT

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
125575512 12557551 1 PS PREZISTA DARUNAVIR ETHANOLATE 1 Oral U U 21976 TABLETS
125575512 12557551 2 SS TRUVADA EMTRICITABINETENOFOVIR DISOPROXIL FUMARATE 1 Unknown 0 TABLET
125575512 12557551 3 SS EMTRIVA EMTRICITABINE 1 Unknown U 0 CAPSULE
125575512 12557551 4 SS TIVICAY DOLUTEGRAVIR SODIUM 1 Unknown U 0 UNSPECIFIED
125575512 12557551 5 SS NORVIR RITONAVIR 1 Unknown U 0 UNSPECIFIED
125575512 12557551 6 SS BARACLUDE ENTECAVIR 1 Unknown U 0 UNSPECIFIED

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125575512 12557551 1 Product used for unknown indication
125575512 12557551 2 Product used for unknown indication
125575512 12557551 3 Product used for unknown indication
125575512 12557551 4 Product used for unknown indication
125575512 12557551 5 Product used for unknown indication
125575512 12557551 6 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
125575512 12557551 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
125575512 12557551 Blood creatinine increased
125575512 12557551 Liver disorder
125575512 12557551 Renal failure

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

no results found

Therapies reported

no results found