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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 121307722 | 12130772 | 2 | F | 20160728 | 20160301 | 20160913 | PER | US-JNJFOC-20160120170 | JANSSEN | 75.00 | YR | E | M | Y | 97.52000 | KG | 20160913 | CN | US | US |
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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 121307722 | 12130772 | 1 | PS | IMODIUM MULTI-SYMPTOM RELIEF | DIMETHICONELOPERAMIDE HYDROCHLORIDE | 1 | Oral | N | 0001107-INV | 20606 | CHEWABLE TABLET | ||||||||
| 121307722 | 12130772 | 2 | SS | IMODIUM MULTI-SYMPTOM RELIEF | DIMETHICONELOPERAMIDE HYDROCHLORIDE | 1 | Oral | 1/3 TO 1 CAPLET | N | 0001107-INV | 20606 | CHEWABLE TABLET | |||||||
| 121307722 | 12130772 | 3 | C | CELEBREX | CELECOXIB | 1 | Unknown | 0 | UNSPECIFIED | ||||||||||
| 121307722 | 12130772 | 4 | C | COLCRYS | COLCHICINE | 1 | Unknown | 0 | UNSPECIFIED | ||||||||||
| 121307722 | 12130772 | 5 | C | TRIAMTERENE. | TRIAMTERENE | 1 | Unknown | 0 | UNSPECIFIED | ||||||||||
| 121307722 | 12130772 | 6 | C | LOSARTAN. | LOSARTAN | 1 | Unknown | 0 | UNSPECIFIED |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 121307722 | 12130772 | 2 | Diarrhoea |
| 121307722 | 12130772 | 3 | Arthritis |
| 121307722 | 12130772 | 4 | Arthritis |
| 121307722 | 12130772 | 5 | Hypertension |
| 121307722 | 12130772 | 6 | Hypertension |
Outcome of event
| no results found |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 121307722 | 12130772 | Drug effect increased | |
| 121307722 | 12130772 | Incorrect dose administered |
Reporting Sources (this data is often not reported and may therefore be missing here)
| no results found |
Therapies reported
| no results found |