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 |