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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 125906081 | 12590608 | 1 | I | 20160609 | 20160726 | 20160726 | EXP | US-AMGEN-USASL2016074886 | AMGEN | 68.00 | YR | E | M | Y | 97.52000 | KG | 20160725 | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 125906081 | 12590608 | 1 | PS | NPLATE | ROMIPLOSTIM | 1 | Unknown | UNK | N | 125268 | POWDER FOR INJECTION | ||||||||
| 125906081 | 12590608 | 2 | C | PROTONIX | PANTOPRAZOLE SODIUM | 1 | 40 MG, QD | 0 | 40 | MG | QD | ||||||||
| 125906081 | 12590608 | 3 | C | MOBIC | MELOXICAM | 1 | 15 MG, QD | 0 | 15 | MG | QD | ||||||||
| 125906081 | 12590608 | 4 | C | LOTREL | AMLODIPINE BESYLATEBENAZEPRIL HYDROCHLORIDE | 1 | 5 MG, QD | 0 | 5 | MG | QD | ||||||||
| 125906081 | 12590608 | 5 | C | TRICOR | FENOFIBRATE | 1 | 160 MG, QD | 0 | 160 | MG | QD | ||||||||
| 125906081 | 12590608 | 6 | C | ANUSOL HC | HYDROCORTISONE | 1 | 0 G, BID | 0 | BID | ||||||||||
| 125906081 | 12590608 | 7 | C | PROMACTA | ELTROMBOPAG OLAMINE | 1 | 50 MG, QD | 0 | 50 | MG | QD |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 125906081 | 12590608 | 1 | Immune thrombocytopenic purpura |
Outcome of event
| Event ID | CASEID | OUTC COD |
|---|---|---|
| 125906081 | 12590608 | OT |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 125906081 | 12590608 | Chronic kidney disease | |
| 125906081 | 12590608 | Contusion | |
| 125906081 | 12590608 | Drug effect decreased | |
| 125906081 | 12590608 | Ecchymosis | |
| 125906081 | 12590608 | Fatigue | |
| 125906081 | 12590608 | Hypoaesthesia | |
| 125906081 | 12590608 | Insomnia | |
| 125906081 | 12590608 | Platelet count abnormal | |
| 125906081 | 12590608 | Weight decreased |
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 |
|---|---|---|---|---|---|---|
| 125906081 | 12590608 | 1 | 201605 | 0 |