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
126166032 12616603 2 F 2015 20160829 20160802 20160901 EXP DK-ABBVIE-16K-044-1690487-00 ABBVIE 50.00 YR F Y 0.00000 20160901 MD DK DK

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
126166032 12616603 1 PS NORVIR RITONAVIR 1 Oral U UNKNOWN 20945 100 MG BID
126166032 12616603 2 SS COMBIVIR LAMIVUDINEIDOVUDINE 1 Unknown U UNKNOWN 0 1 DF TABLET BID
126166032 12616603 3 SS DARUNAVIR DARUNAVIR 1 Unknown U UNKNOWN 0 600 MG BID
126166032 12616603 4 SS DOLUTEGRAVIR DOLUTEGRAVIR 1 Unknown U UNKNOWN 0
126166032 12616603 5 SS MARAVIROC MARAVIROC 1 Unknown U UNKNOWN 0 150 MG BID
126166032 12616603 6 SS RETROVIR ZIDOVUDINE 1 Unknown U UNKNOWN 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126166032 12616603 1 Acquired immunodeficiency syndrome
126166032 12616603 2 Acquired immunodeficiency syndrome
126166032 12616603 3 Acquired immunodeficiency syndrome
126166032 12616603 4 Acquired immunodeficiency syndrome
126166032 12616603 5 Acquired immunodeficiency syndrome
126166032 12616603 6 Acquired immunodeficiency syndrome

Outcome of event

Event ID CASEID OUTC COD
126166032 12616603 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
126166032 12616603 Anaemia
126166032 12616603 Pathogen resistance
126166032 12616603 Treatment noncompliance
126166032 12616603 Weight decreased

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

no results found

Therapies reported

no results found