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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 127237402 | 12723740 | 2 | F | 20160820 | 20160913 | 20160908 | 20160918 | PER | PHEH2016US022323 | NOVARTIS | 56.71 | YR | M | Y | 90.70000 | KG | 20160918 | CN | COUNTRY NOT SPECIFIED | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 127237402 | 12723740 | 1 | PS | MYFORTIC | MYCOPHENOLATE SODIUM | 1 | Oral | 540 MG, BID | 50791 | 540 | MG | BID |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 127237402 | 12723740 | 1 | Heart transplant |
Outcome of event
| Event ID | CASEID | OUTC COD |
|---|---|---|
| 127237402 | 12723740 | HO |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 127237402 | 12723740 | Asthenia | |
| 127237402 | 12723740 | Dehydration | |
| 127237402 | 12723740 | Hypertension | |
| 127237402 | 12723740 | Muscle spasms | |
| 127237402 | 12723740 | Musculoskeletal pain | |
| 127237402 | 12723740 | Product use issue |
Reporting Sources (this data is often not reported and may therefore be missing here)
| no results found |
Therapies reported
| Event ID | CASEID | DSG DRUG SEQ | START DT | END DT | DUR | DUR COD |
|---|---|---|---|---|---|---|
| 127237402 | 12723740 | 1 | 2010 | 0 |