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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 1170670711 | 11706707 | 11 | F | 201508 | 20160908 | 20151106 | 20160922 | EXP | CA-VALIDUS PHARMACEUTICALS LLC-CA-2015VAL000689 | VALIDUS | 0.00 | Y | 0.00000 | 20160922 | CN | CA | CA |
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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 1170670711 | 11706707 | 1 | PS | METOPROLOL TARTRATE. | METOPROLOL TARTRATE | 1 | Oral | 200 MG, QD | U | 17963 | 200 | MG | |||||||
| 1170670711 | 11706707 | 2 | SS | SANDOSTATIN | OCTREOTIDE ACETATE | 1 | Intramuscular | 30 MG, QMO (EVERY 4 WEEKS) SANDOSTATIN LAR | U | 350796 | 0 | 30 | MG | ||||||
| 1170670711 | 11706707 | 3 | C | DILAUDID | HYDROMORPHONE HYDROCHLORIDE | 1 | UNK | Y | 0 | ||||||||||
| 1170670711 | 11706707 | 4 | C | ACETAMINOPHEN. | ACETAMINOPHEN | 1 | 500 MG, PRN | U | 0 | 500 | MG | ||||||||
| 1170670711 | 11706707 | 5 | C | MOXIFLOXACIN. | MOXIFLOXACIN | 1 | UNK | U | 0 |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 1170670711 | 11706707 | 1 | Product used for unknown indication |
| 1170670711 | 11706707 | 2 | Neuroendocrine tumour |
| 1170670711 | 11706707 | 3 | Product used for unknown indication |
| 1170670711 | 11706707 | 4 | Product used for unknown indication |
| 1170670711 | 11706707 | 5 | Product used for unknown indication |
Outcome of event
| Event ID | CASEID | OUTC COD |
|---|---|---|
| 1170670711 | 11706707 | HO |
| 1170670711 | 11706707 | OT |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 1170670711 | 11706707 | Abdominal discomfort | |
| 1170670711 | 11706707 | Abdominal distension | |
| 1170670711 | 11706707 | Abdominal pain | |
| 1170670711 | 11706707 | Abdominal pain upper | |
| 1170670711 | 11706707 | Blood pressure increased | |
| 1170670711 | 11706707 | Diarrhoea | |
| 1170670711 | 11706707 | Discomfort | |
| 1170670711 | 11706707 | Dizziness | |
| 1170670711 | 11706707 | Dyspnoea | |
| 1170670711 | 11706707 | Fatigue | |
| 1170670711 | 11706707 | Feeling hot | |
| 1170670711 | 11706707 | Gastrointestinal disorder | |
| 1170670711 | 11706707 | Headache | |
| 1170670711 | 11706707 | Hepatic pain | |
| 1170670711 | 11706707 | Influenza | |
| 1170670711 | 11706707 | Malignant neoplasm progression | |
| 1170670711 | 11706707 | Metastases to liver | |
| 1170670711 | 11706707 | Myalgia | |
| 1170670711 | 11706707 | Nausea | |
| 1170670711 | 11706707 | Needle issue | |
| 1170670711 | 11706707 | Pleural effusion | |
| 1170670711 | 11706707 | Pneumonia |
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 |
|---|---|---|---|---|---|---|
| 1170670711 | 11706707 | 2 | 20150804 | 0 |