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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 126783121 | 12678312 | 1 | I | 20160730 | 20160809 | 20160823 | 20160823 | EXP | GB-MHRA-TPP17622316C2468555YC1469892159280 | GB-TEVA-684589ACC | TEVA | 91.00 | YR | F | Y | 53.00000 | KG | 20160823 | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 126783121 | 12678312 | 1 | PS | NITROFURANTOIN. | NITROFURANTOIN | 1 | U | U | 73696 | ||||||||||
| 126783121 | 12678312 | 2 | C | AMOXICILLIN. | AMOXICILLIN | 1 | 15 ML DAILY; | 270 | ML | 0 | 5 | ML | TID | ||||||
| 126783121 | 12678312 | 3 | C | CITALOPRAM | CITALOPRAM HYDROBROMIDE | 1 | 1 DOSAGE FORMS DAILY; 1 DOSAGE FORM, EVERY MORNING | 340 | DF | 0 | 1 | DF | QD | ||||||
| 126783121 | 12678312 | 4 | C | FERROUS GLUCONATE | FERROUS GLUCONATE | 1 | 2 DOSAGE FORMS DAILY; | 30 | DF | 0 | 2 | DF | QD | ||||||
| 126783121 | 12678312 | 5 | C | MELOXICAM. | MELOXICAM | 1 | 1 DOSAGE FORMS DAILY; 1 DOSAGE FORM, EACH MORNING. | 340 | DF | 0 | 1 | DF | QD | ||||||
| 126783121 | 12678312 | 6 | C | OMEPRAZOLE. | OMEPRAZOLE | 1 | 1 DOSAGE FORM, EVERY MORNING. | 340 | DF | 0 | 1 | DF | QD | ||||||
| 126783121 | 12678312 | 7 | C | PARACETAMOL | ACETAMINOPHEN | 1 | 8 DOSAGE FORMS DAILY; | 2720 | DF | 0 | 2 | DF | QID | ||||||
| 126783121 | 12678312 | 8 | C | PIVMECILLINAM | PENICILLIN | 1 | TWO STAT AND ONE THREE TIMES A DAY THEREAFTER | 0 | |||||||||||
| 126783121 | 12678312 | 9 | C | TRIMETHOPRIM. | TRIMETHOPRIM | 1 | 2 DOSAGE FORMS DAILY; | 38 | DF | 0 | 1 | DF | BID |
Indications of drugs used
| no results found |
Outcome of event
| Event ID | CASEID | OUTC COD |
|---|---|---|
| 126783121 | 12678312 | DS |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 126783121 | 12678312 | 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 |
|---|---|---|---|---|---|---|
| 126783121 | 12678312 | 1 | 20160730 | 0 | ||
| 126783121 | 12678312 | 2 | 20160712 | 20160719 | 0 | |
| 126783121 | 12678312 | 3 | 20150825 | 0 | ||
| 126783121 | 12678312 | 4 | 20160715 | 0 | ||
| 126783121 | 12678312 | 5 | 20150825 | 0 | ||
| 126783121 | 12678312 | 6 | 20150825 | 0 | ||
| 126783121 | 12678312 | 7 | 20150825 | 0 | ||
| 126783121 | 12678312 | 8 | 20160730 | 0 | ||
| 126783121 | 12678312 | 9 | 20160711 | 20160717 | 0 |