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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 126977391 | 12697739 | 1 | I | 20160825 | 20160830 | 20160830 | EXP | US-STRIDES ARCOLAB LIMITED-2016SP012659 | STRIDES | PATEL SJ, KUTEN SA, MUSICK WL, GABER AO, MONSOUR HP, KNIGHT RJ. COMBINATION DRUG PRODUCTS FOR HIV-A WORD OF CAUTION FOR THE TRANSPLANT CLINICIAN. AM J TRANSPLANT. 2016;16(8):2479-2482 | 0.00 | Y | 0.00000 | 20160830 | OT | US | US |
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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 126977391 | 12697739 | 1 | PS | TACROLIMUS. | TACROLIMUS | 1 | 3 MG, EVERY 12 HRS | U | 90687 | 3 | MG | ||||||||
| 126977391 | 12697739 | 2 | I | TACROLIMUS. | TACROLIMUS | 1 | 3MG | U | 90687 | ||||||||||
| 126977391 | 12697739 | 3 | I | TACROLIMUS. | TACROLIMUS | 1 | 0.5 MG, 2 TIMES A WEEK | U | 90687 | .5 | MG | ||||||||
| 126977391 | 12697739 | 4 | I | TACROLIMUS. | TACROLIMUS | 1 | 3 MG, EVERY 12 HRS | U | 90687 | 3 | MG | ||||||||
| 126977391 | 12697739 | 5 | I | STRIBILD | COBICISTATELVITEGRAVIREMTRICITABINETENOFOVIR DISOPROXIL FUMARATE | 1 | 1 DF, QD | 0 | 1 | DF | TABLET | ||||||||
| 126977391 | 12697739 | 6 | I | STRIBILD | COBICISTATELVITEGRAVIREMTRICITABINETENOFOVIR DISOPROXIL FUMARATE | 1 | UNK | 0 | TABLET |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 126977391 | 12697739 | 1 | Immunosuppression |
| 126977391 | 12697739 | 5 | HIV infection |
Outcome of event
| Event ID | CASEID | OUTC COD |
|---|---|---|
| 126977391 | 12697739 | OT |
| 126977391 | 12697739 | HO |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 126977391 | 12697739 | Acute kidney injury | |
| 126977391 | 12697739 | Diabetes mellitus inadequate control | |
| 126977391 | 12697739 | Diarrhoea | |
| 126977391 | 12697739 | Drug interaction | |
| 126977391 | 12697739 | Headache | |
| 126977391 | 12697739 | Nausea | |
| 126977391 | 12697739 | Renal impairment | |
| 126977391 | 12697739 | Toxicity to various agents | |
| 126977391 | 12697739 | Visual impairment | |
| 126977391 | 12697739 | Vomiting |
Reporting Sources (this data is often not reported and may therefore be missing here)
| no results found |
Therapies reported
| no results found |