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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 122968122 | 12296812 | 2 | F | 1989 | 20160406 | 20160422 | 20160721 | PER | US-B.I. PHARMACEUTICALS,INC./RIDGEFIELD-2016-BI-21772BP | BOEHRINGER INGELHEIM | 0.00 | M | Y | 0.00000 | 20160721 | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 122968122 | 12296812 | 1 | PS | ZANTAC | RANITIDINE HYDROCHLORIDE | 1 | Oral | 20520 | TABLET | ||||||||||
| 122968122 | 12296812 | 2 | SS | ZANTAC | RANITIDINE HYDROCHLORIDE | 1 | Oral | DAILY DOSE: MORE THAN 2 TABLETS PER DAY | 20520 | TABLET |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 122968122 | 12296812 | 1 | Dyspepsia |
Outcome of event
| no results found |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 122968122 | 12296812 | Dyspepsia | |
| 122968122 | 12296812 | Incorrect drug administration duration | |
| 122968122 | 12296812 | Medication error |
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 |
|---|---|---|---|---|---|---|
| 122968122 | 12296812 | 1 | 1989 | 0 |