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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 126586453 | 12658645 | 3 | F | 2016 | 20160907 | 20160817 | 20160921 | EXP | GB-MHRA-EYC 00143005 | GB-LUPIN PHARMACEUTICALS INC.-E2B_00005979 | LUPIN | 47.00 | YR | F | Y | 58.00000 | KG | 20160921 | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 126586453 | 12658645 | 1 | PS | CETIRIZINE HYDROCHLORIDE. | CETIRIZINE HYDROCHLORIDE | 1 | Oral | 10 MG | Y | U | CB13L51 | 206793 | |||||||
| 126586453 | 12658645 | 2 | SS | SERTRALINE | SERTRALINE HYDROCHLORIDE | 1 | Oral | 100 MG | U | UNKNOWN | 77670 | ||||||||
| 126586453 | 12658645 | 3 | SS | SERTRALINE | SERTRALINE HYDROCHLORIDE | 1 | Oral | 150MG | 2758097 | 0 | |||||||||
| 126586453 | 12658645 | 4 | SS | SERTRALINE | SERTRALINE HYDROCHLORIDE | 1 | Oral | 100MG | 2758097 | 0 | |||||||||
| 126586453 | 12658645 | 5 | C | Loratidine | LORATADINE | 1 | Unknown | 0 | |||||||||||
| 126586453 | 12658645 | 6 | C | Paracetamol | ACETAMINOPHEN | 1 | Unknown | 0 |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 126586453 | 12658645 | 1 | Multiple allergies |
| 126586453 | 12658645 | 2 | Depression |
| 126586453 | 12658645 | 3 | Depression |
| 126586453 | 12658645 | 5 | Product used for unknown indication |
| 126586453 | 12658645 | 6 | Headache |
Outcome of event
| Event ID | CASEID | OUTC COD |
|---|---|---|
| 126586453 | 12658645 | OT |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 126586453 | 12658645 | Abdominal discomfort | |
| 126586453 | 12658645 | Blood pressure systolic increased | |
| 126586453 | 12658645 | Depression | |
| 126586453 | 12658645 | Headache | |
| 126586453 | 12658645 | Inhibitory drug interaction |
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 |
|---|---|---|---|---|---|---|
| 126586453 | 12658645 | 1 | 20160713 | 20160722 | 0 | |
| 126586453 | 12658645 | 2 | 2016 | 0 | ||
| 126586453 | 12658645 | 3 | 2016 | 2016 | 0 | |
| 126586453 | 12658645 | 4 | 2016 | 2016 | 0 |