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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 126957323 | 12695732 | 3 | F | 20160819 | 20160906 | 20160829 | 20160913 | EXP | BR-ALEXION PHARMACEUTICALS INC.-A201605978 | ALEXION | 0.00 | F | Y | 0.00000 | 20160913 | CN | BR | BR |
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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 126957323 | 12695732 | 1 | PS | SOLIRIS | ECULIZUMAB | 1 | Intravenous (not otherwise specified) | UNK | U | 125166 | CONCENTRATE FOR SOLUTION FOR INFUSION | ||||||||
| 126957323 | 12695732 | 2 | C | METILDOPA | METHYLDOPA | 1 | Unknown | 500 MG, Q8H (2TABLETS EVERY 8 HOURS) | 0 | 500 | MG | TABLET | Q8H | ||||||
| 126957323 | 12695732 | 3 | C | NIFEDIPINE. | NIFEDIPINE | 1 | Unknown | 20 MG, Q4H (1 TABLET EVERY 4 HOURS) | 0 | 20 | MG | TABLET | Q4H | ||||||
| 126957323 | 12695732 | 4 | C | HYDRALAZINE | HYDRALAZINE HYDROCHLORIDE | 1 | Unknown | 25 MG, Q8H (1 TABLET EVERY 8 HOURS) | 0 | 25 | MG | Q8H | |||||||
| 126957323 | 12695732 | 5 | C | FUROSEMIDE. | FUROSEMIDE | 1 | Unknown | 40 MG, Q8H (EVERY 8 HOURS) | 0 | 40 | MG | TABLET | Q8H | ||||||
| 126957323 | 12695732 | 6 | C | CALCIUM CARBONATE. | CALCIUM CARBONATE | 1 | Unknown | 500 MG, Q2H (1 TABLET 2 HOURS AFTER LUNCH) | 0 | 500 | MG | TABLET | Q2H | ||||||
| 126957323 | 12695732 | 7 | C | FOLIC ACID. | FOLIC ACID | 1 | Unknown | 5 MG, QD (1 TABLET AT 8AM) | 0 | 5 | MG | QD | |||||||
| 126957323 | 12695732 | 8 | C | UTROGESTAN | PROGESTERONE | 1 | Unknown | 200 MG, UNK ( 1 OVULO A NOITE) | 0 | 200 | MG | ||||||||
| 126957323 | 12695732 | 9 | C | MICONAZOLE. | MICONAZOLE | 1 | Unknown | UNK, ( 1 APLICACAO-7 NOITES) | 0 |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 126957323 | 12695732 | 1 | Haemolytic uraemic syndrome |
| 126957323 | 12695732 | 2 | Product used for unknown indication |
| 126957323 | 12695732 | 3 | Product used for unknown indication |
| 126957323 | 12695732 | 4 | Product used for unknown indication |
| 126957323 | 12695732 | 5 | Product used for unknown indication |
| 126957323 | 12695732 | 6 | Product used for unknown indication |
| 126957323 | 12695732 | 7 | Product used for unknown indication |
| 126957323 | 12695732 | 8 | Product used for unknown indication |
| 126957323 | 12695732 | 9 | Product used for unknown indication |
Outcome of event
| Event ID | CASEID | OUTC COD |
|---|---|---|
| 126957323 | 12695732 | OT |
| 126957323 | 12695732 | HO |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 126957323 | 12695732 | Bacteraemia | |
| 126957323 | 12695732 | Device related infection | |
| 126957323 | 12695732 | Exposure during pregnancy | |
| 126957323 | 12695732 | Premature delivery | |
| 126957323 | 12695732 | Premature labour | |
| 126957323 | 12695732 | Procedural headache | |
| 126957323 | 12695732 | Pyrexia | |
| 126957323 | 12695732 | Vaginal haemorrhage |
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 |
|---|---|---|---|---|---|---|
| 126957323 | 12695732 | 1 | 20160809 | 0 |