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
125252464 12525246 4 F 201606 20160808 20160704 20160812 EXP GB-JNJFOC-20160624732 JANSSEN 49.31 YR A M Y 0.00000 20160812 CN 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
125252464 12525246 1 PS PREZISTA DARUNAVIR ETHANOLATE 1 Unknown U U UNKNOWN 21976 800 MG TABLETS
125252464 12525246 2 SS NORVIR RITONAVIR 1 Unknown U 0 100 MG TABLET
125252464 12525246 3 SS RALTEGRAVIR. RALTEGRAVIR 1 Unknown U 0 400 MG TABLET
125252464 12525246 4 SS TENOFOVIR DISOPROXIL FUMARATE. TENOFOVIR DISOPROXIL FUMARATE 1 Unknown U 0 245 MG TABLET

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125252464 12525246 1 Product used for unknown indication
125252464 12525246 2 Product used for unknown indication
125252464 12525246 3 Product used for unknown indication
125252464 12525246 4 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
125252464 12525246 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
125252464 12525246 Activities of daily living impaired
125252464 12525246 Hypersomnia
125252464 12525246 Malaise
125252464 12525246 Seizure
125252464 12525246 Viral load increased
125252464 12525246 Vomiting

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

no results found

Therapies reported

no results found