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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 126586764 | 12658676 | 4 | F | 20160806 | 20160909 | 20160817 | 20160919 | EXP | US-ALEXION-A201605959 | ALEXION | 44.25 | YR | F | Y | 0.00000 | 20160919 | CN | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 126586764 | 12658676 | 1 | PS | SOLIRIS | ECULIZUMAB | 1 | Intravenous (not otherwise specified) | 1200 MG, Q2W | 14226.5059 | MG | Y | 125166 | 1200 | MG | CONCENTRATE FOR SOLUTION FOR INFUSION | QOW | |||
| 126586764 | 12658676 | 2 | C | BENADRYL | DIPHENHYDRAMINE HYDROCHLORIDE | 1 | Unknown | 0 | |||||||||||
| 126586764 | 12658676 | 3 | C | AMLODIPINE | AMLODIPINE BESYLATE | 1 | Unknown | UNK, QD | 0 | QD | |||||||||
| 126586764 | 12658676 | 4 | C | CLONIDINE. | CLONIDINE | 1 | Unknown | UNK, PRN | 0 | /yr | |||||||||
| 126586764 | 12658676 | 5 | C | LISINOPRIL. | LISINOPRIL | 1 | Unknown | UNK, PRN | 0 | /yr | |||||||||
| 126586764 | 12658676 | 6 | C | KEPPRA | LEVETIRACETAM | 1 | Unknown | UNK | 0 |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 126586764 | 12658676 | 1 | Haemolytic uraemic syndrome |
| 126586764 | 12658676 | 2 | Product used for unknown indication |
| 126586764 | 12658676 | 3 | Product used for unknown indication |
| 126586764 | 12658676 | 4 | Product used for unknown indication |
| 126586764 | 12658676 | 5 | Product used for unknown indication |
| 126586764 | 12658676 | 6 | Product used for unknown indication |
Outcome of event
| Event ID | CASEID | OUTC COD |
|---|---|---|
| 126586764 | 12658676 | OT |
| 126586764 | 12658676 | HO |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 126586764 | 12658676 | Headache | |
| 126586764 | 12658676 | Hypertension | |
| 126586764 | 12658676 | Nausea | |
| 126586764 | 12658676 | Pain | |
| 126586764 | 12658676 | Seizure | |
| 126586764 | 12658676 | Vomiting |
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 |
|---|---|---|---|---|---|---|
| 126586764 | 12658676 | 1 | 20150225 | 20160826 | 0 |