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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 125613871 | 12561387 | 1 | I | 20160621 | 20160705 | 20160715 | 20160715 | EXP | GB-MHRA-TPP25093065C1824525YC1466502725590 | GB-TEVA-674538ACC | TEVA | 85.00 | YR | F | Y | 70.00000 | KG | 20160715 | MD | GB | GB |
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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 125613871 | 12561387 | 1 | PS | NITROFURANTOIN. | NITROFURANTOIN | 1 | U | U | 73652 | ||||||||||
| 125613871 | 12561387 | 2 | C | AMLODIPINE | AMLODIPINE BESYLATE | 1 | 1 DOSAGE FORMS DAILY; | 116.958333 | DF | 0 | 1 | DF | QD | ||||||
| 125613871 | 12561387 | 3 | C | ASPIRIN. | ASPIRIN | 1 | 1 DOSAGE FORMS DAILY; | 116.958333 | DF | 0 | 1 | DF | QD | ||||||
| 125613871 | 12561387 | 4 | C | CHLORAMPHENICOL | CHLORAMPHENICOL | 1 | APPLY 4 TIMES A DAY FOR 2 DAYS AND CONTINUE FOR... | 0 | |||||||||||
| 125613871 | 12561387 | 5 | C | DOXAZOSIN | DOXAZOSINDOXAZOSIN MESYLATE | 1 | 1 DOSAGE FORMS DAILY; | 116.958333 | DF | 0 | 1 | DF | QD | ||||||
| 125613871 | 12561387 | 6 | C | LOSARTAN. | LOSARTAN | 1 | 1 DOSAGE FORMS DAILY; | 116.958333 | DF | 0 | 1 | DF | QD | ||||||
| 125613871 | 12561387 | 7 | C | OMEPRAZOLE. | OMEPRAZOLE | 1 | 1 DOSAGE FORMS DAILY; MORNING | 40 | DF | 0 | 1 | DF | QD | ||||||
| 125613871 | 12561387 | 8 | C | PRAVASTATIN. | PRAVASTATIN | 1 | 1 DOSAGE FORMS DAILY; AT NIGHT | 116.958333 | DF | 0 | 1 | DF | QD | ||||||
| 125613871 | 12561387 | 9 | C | SODIUM CHLORIDE. | SODIUM CHLORIDE | 1 | DECR DOSAGE AS DIRECTED | 0 |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 125613871 | 12561387 | 8 | Blood cholesterol increased |
Outcome of event
| Event ID | CASEID | OUTC COD |
|---|---|---|
| 125613871 | 12561387 | OT |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 125613871 | 12561387 | Dyspnoea | |
| 125613871 | 12561387 | 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 |
|---|---|---|---|---|---|---|
| 125613871 | 12561387 | 1 | 20160621 | 0 | ||
| 125613871 | 12561387 | 2 | 20160225 | 0 | ||
| 125613871 | 12561387 | 3 | 20160225 | 0 | ||
| 125613871 | 12561387 | 4 | 20160512 | 0 | ||
| 125613871 | 12561387 | 5 | 20160225 | 0 | ||
| 125613871 | 12561387 | 6 | 20160225 | 0 | ||
| 125613871 | 12561387 | 7 | 20160512 | 0 | ||
| 125613871 | 12561387 | 8 | 20160225 | 0 | ||
| 125613871 | 12561387 | 9 | 20160525 | 0 |