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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 126799842 | 12679984 | 2 | F | 20160408 | 20160907 | 20160824 | 20160919 | EXP | GB-SUN PHARMACEUTICAL INDUSTRIES LTD-2016RR-122402 | RANBAXY | 67.00 | YR | M | Y | 0.00000 | 20160919 | OT | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 126799842 | 12679984 | 1 | PS | LANSOPRAZOLE. | LANSOPRAZOLE | 1 | Oral | 30 MG, DAILY | Y | U | 202637 | 30 | MG | ||||||
| 126799842 | 12679984 | 2 | SS | SERTRALINE | SERTRALINE HYDROCHLORIDE | 1 | Oral | SUSPENDED DURING ADMISSION FOR 2 DAYS, BUT RESTARTED DUE TO CLINICAL NEED | Y | 0 | |||||||||
| 126799842 | 12679984 | 3 | C | FOLIC ACID. | FOLIC ACID | 1 | Oral | 5 MG, DAILY | U | U | 0 | 5 | MG | ||||||
| 126799842 | 12679984 | 4 | C | ONDANSETRON | ONDANSETRON | 1 | Oral | AS REQUIRED. | U | U | 0 | 4 | MG | Q8H | |||||
| 126799842 | 12679984 | 5 | C | PROCYCLIDINE | PROCYCLIDINE | 1 | Oral | AT NIGHT | U | U | 0 | 5 | MG | ||||||
| 126799842 | 12679984 | 6 | C | RISPERIDONE. | RISPERIDONE | 1 | Oral | AT NIGHT. | U | U | 0 | 3 | MG | ||||||
| 126799842 | 12679984 | 7 | C | SOLIFENACIN | SOLIFENACIN | 1 | Oral | EVERY MORNING | U | U | 0 | 5 | MG | ||||||
| 126799842 | 12679984 | 8 | C | TAMSULOSIN | TAMSULOSIN | 1 | Oral | EVERY MORNING | U | U | 0 | 400 | UG |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 126799842 | 12679984 | 1 | Prophylaxis against gastrointestinal ulcer |
| 126799842 | 12679984 | 2 | Product used for unknown indication |
| 126799842 | 12679984 | 3 | Product used for unknown indication |
| 126799842 | 12679984 | 4 | Product used for unknown indication |
| 126799842 | 12679984 | 5 | Product used for unknown indication |
| 126799842 | 12679984 | 6 | Product used for unknown indication |
| 126799842 | 12679984 | 7 | Product used for unknown indication |
| 126799842 | 12679984 | 8 | Product used for unknown indication |
Outcome of event
| Event ID | CASEID | OUTC COD |
|---|---|---|
| 126799842 | 12679984 | HO |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 126799842 | 12679984 | Hyponatraemia |
Reporting Sources (this data is often not reported and may therefore be missing here)
| no results found |
Therapies reported
| no results found |