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
125584021 12558402 1 I 20160707 20160714 20160714 EXP AT-ABBVIE-16P-009-1670629-00 ABBVIE 0.00 F Y 0.00000 20160714 MD AT 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
125584021 12558402 1 PS NORVIR RITONAVIR 1 Oral REGIMEN #1 U UNKNOWN 20945
125584021 12558402 2 SS TRUVADA EMTRICITABINETENOFOVIR DISOPROXIL FUMARATE 1 Unknown REGIMEN #1 UNKNOWN 0 TABLET
125584021 12558402 3 SS EMTRIVA EMTRICITABINE 1 Unknown REGIMEN #1 U UNKNOWN 0 CAPSULE
125584021 12558402 4 SS TIVICAY DOLUTEGRAVIR SODIUM 1 Unknown REGIMEN #1 U UNKNOWN 0 TABLET
125584021 12558402 5 SS PREZISTA DARUNAVIR ETHANOLATE 1 Unknown REGIMEN #1 U UNKNOWN 0
125584021 12558402 6 SS BARACLUDE ENTECAVIR 1 Unknown REGIMEN #1 U UNKNOWN 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125584021 12558402 1 Product used for unknown indication
125584021 12558402 2 Product used for unknown indication
125584021 12558402 3 Product used for unknown indication
125584021 12558402 4 Product used for unknown indication
125584021 12558402 5 Product used for unknown indication
125584021 12558402 6 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
125584021 12558402 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
125584021 12558402 Blood creatinine increased
125584021 12558402 Liver transplant
125584021 12558402 Renal failure

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

no results found

Therapies reported

no results found