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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 127899981 | 12789998 | 1 | I | 2005 | 20160706 | 20160928 | 20160928 | EXP | US-DSJP-DSU-2016-123832 | DAIICHI | 0.00 | Y | 0.00000 | 20160928 | MD | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 127899981 | 12789998 | 1 | PS | BENICAR | OLMESARTAN MEDOXOMIL | 1 | Oral | 40 MG, QD | U | 21286 | 40 | MG | TABLET | QD | |||||
| 127899981 | 12789998 | 2 | SS | BENICAR | OLMESARTAN MEDOXOMIL | 1 | 20 MG, UNK | U | 21286 | 20 | MG | TABLET | |||||||
| 127899981 | 12789998 | 3 | SS | LEVOFLOXACIN. | LEVOFLOXACIN | 1 | UNK | 0 | |||||||||||
| 127899981 | 12789998 | 4 | SS | METRONIDAZOLE. | METRONIDAZOLE | 1 | UNK | 0 | |||||||||||
| 127899981 | 12789998 | 5 | C | TOPROL XL | METOPROLOL SUCCINATE | 1 | Oral | 25 MG, QD | 0 | 25 | MG | TABLET | QD | ||||||
| 127899981 | 12789998 | 6 | C | SYNTHROID | LEVOTHYROXINE SODIUM | 1 | 75 ?G, QD | 0 | 75 | UG | TABLET | QD |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 127899981 | 12789998 | 1 | Hypertension |
| 127899981 | 12789998 | 3 | Product used for unknown indication |
| 127899981 | 12789998 | 4 | Clostridium difficile infection |
| 127899981 | 12789998 | 5 | Essential hypertension |
| 127899981 | 12789998 | 6 | Product used for unknown indication |
Outcome of event
| Event ID | CASEID | OUTC COD |
|---|---|---|
| 127899981 | 12789998 | OT |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 127899981 | 12789998 | Alopecia | |
| 127899981 | 12789998 | Clostridium difficile infection | |
| 127899981 | 12789998 | Diverticulum | |
| 127899981 | 12789998 | Duodenal ulcer | |
| 127899981 | 12789998 | Gastrooesophageal reflux disease | |
| 127899981 | 12789998 | Haemorrhoids | |
| 127899981 | 12789998 | Hiatus hernia | |
| 127899981 | 12789998 | Irritable bowel syndrome | |
| 127899981 | 12789998 | Malabsorption | |
| 127899981 | 12789998 | Oesophageal stenosis |
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 |
|---|---|---|---|---|---|---|
| 127899981 | 12789998 | 1 | 200505 | 201508 | 0 | |
| 127899981 | 12789998 | 3 | 201405 | 0 | ||
| 127899981 | 12789998 | 4 | 2014 | 0 |