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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 122971792 | 12297179 | 2 | F | 2008 | 20160826 | 20160422 | 20160902 | EXP | US-DSJP-DSU-2015-133248 | DAIICHI | 0.00 | Y | 0.00000 | 20160902 | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 122971792 | 12297179 | 1 | PS | BENICAR | OLMESARTAN MEDOXOMIL | 1 | UNK | Y | 21286 | TABLET | |||||||||
| 122971792 | 12297179 | 2 | SS | BENICAR | OLMESARTAN MEDOXOMIL | 1 | 40 MG, UNK | Y | 21286 | 40 | MG | TABLET | |||||||
| 122971792 | 12297179 | 3 | SS | BENICAR | OLMESARTAN MEDOXOMIL | 1 | Oral | 20 MG, QD | Y | 21286 | 20 | MG | TABLET | QD | |||||
| 122971792 | 12297179 | 4 | C | HYDROMORPHONE | HYDROMORPHONE | 1 | UNK | 0 | |||||||||||
| 122971792 | 12297179 | 5 | C | HYDROCODONE BITARTRATE AND ACETAMINOPHEN | ACETAMINOPHENHYDROCODONE BITARTRATE | 1 | UNK | 0 | |||||||||||
| 122971792 | 12297179 | 6 | C | TRAMADOL. | TRAMADOL | 1 | Oral | 50 MG, PRN | 0 | 50 | MG | ||||||||
| 122971792 | 12297179 | 7 | C | AMITRIPTYLINE | AMITRIPTYLINE | 1 | UNK | 0 | |||||||||||
| 122971792 | 12297179 | 8 | C | ZOFRAN | ONDANSETRON HYDROCHLORIDE | 1 | UNK | 0 | |||||||||||
| 122971792 | 12297179 | 9 | C | DILAUDID | HYDROMORPHONE HYDROCHLORIDE | 1 | UNK | 0 | |||||||||||
| 122971792 | 12297179 | 10 | C | PRILOSEC | OMEPRAZOLE MAGNESIUM | 1 | UNK | 0 | |||||||||||
| 122971792 | 12297179 | 11 | C | PROTONIX | PANTOPRAZOLE SODIUM | 1 | UNK | 0 |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 122971792 | 12297179 | 1 | Hypertension |
| 122971792 | 12297179 | 4 | Pain |
| 122971792 | 12297179 | 5 | Pain |
| 122971792 | 12297179 | 6 | Pain |
| 122971792 | 12297179 | 7 | Pain |
| 122971792 | 12297179 | 8 | Product used for unknown indication |
| 122971792 | 12297179 | 9 | Product used for unknown indication |
| 122971792 | 12297179 | 10 | Product used for unknown indication |
| 122971792 | 12297179 | 11 | Product used for unknown indication |
Outcome of event
| Event ID | CASEID | OUTC COD |
|---|---|---|
| 122971792 | 12297179 | HO |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 122971792 | 12297179 | Coeliac artery occlusion | |
| 122971792 | 12297179 | Diverticulum intestinal | |
| 122971792 | 12297179 | Duodenitis | |
| 122971792 | 12297179 | Erosive oesophagitis | |
| 122971792 | 12297179 | Gastrooesophageal reflux disease | |
| 122971792 | 12297179 | Haematochezia | |
| 122971792 | 12297179 | Haemorrhoids | |
| 122971792 | 12297179 | Helicobacter infection | |
| 122971792 | 12297179 | Hiatus hernia | |
| 122971792 | 12297179 | Intestinal ischaemia | |
| 122971792 | 12297179 | Leukocytosis | |
| 122971792 | 12297179 | Malabsorption | |
| 122971792 | 12297179 | Mesenteric artery stenosis | |
| 122971792 | 12297179 | Oesophageal stenosis | |
| 122971792 | 12297179 | Pancreatitis | |
| 122971792 | 12297179 | Peptic ulcer | |
| 122971792 | 12297179 | Polyp | |
| 122971792 | 12297179 | Upper gastrointestinal haemorrhage |
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 |
|---|---|---|---|---|---|---|
| 122971792 | 12297179 | 1 | 200701 | 0 | ||
| 122971792 | 12297179 | 2 | 200807 | 200904 | 0 |