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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 119303853 | 11930385 | 3 | F | 20160112 | 20160120 | 20160901 | PER | PHEH2016US001233 | NOVARTIS | 0.00 | F | Y | 0.00000 | 20160901 | MD | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 119303853 | 11930385 | 1 | PS | PROMACTA | ELTROMBOPAG OLAMINE | 1 | Unknown | 25 MG, (ONE IN EVERY THIRD DAY) | U | 22291 | 25 | MG | |||||||
| 119303853 | 11930385 | 2 | C | ESCITALOPRAM | ESCITALOPRAM OXALATE | 1 | Unknown | U | 0 |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 119303853 | 11930385 | 1 | Product used for unknown indication |
| 119303853 | 11930385 | 2 | Product used for unknown indication |
Outcome of event
| no results found |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 119303853 | 11930385 | Arthralgia | |
| 119303853 | 11930385 | Contusion | |
| 119303853 | 11930385 | Erythema | |
| 119303853 | 11930385 | Headache | |
| 119303853 | 11930385 | Myalgia | |
| 119303853 | 11930385 | Pruritus | |
| 119303853 | 11930385 | Temperature intolerance |
Reporting Sources (this data is often not reported and may therefore be missing here)
| no results found |
Therapies reported
| no results found |