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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 119411202 | 11941120 | 2 | F | 20160809 | 20160122 | 20160815 | EXP | CA-009507513-1601CAN006984 | MERCK | 70.00 | YR | F | Y | 65.00000 | KG | 20160815 | OT | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 119411202 | 11941120 | 1 | PS | COZAAR | LOSARTAN POTASSIUM | 1 | Unknown | UNK | U | 20386 | TABLET | ||||||||
| 119411202 | 11941120 | 2 | SS | MICARDIS PLUS | HYDROCHLOROTHIAZIDETELMISARTAN | 1 | Oral | UNK | U | U | 0 | TABLET | |||||||
| 119411202 | 11941120 | 3 | SS | RITUXAN | RITUXIMAB | 1 | Intravenous (not otherwise specified) | 1000 MG, INTRAVENOUS (NOT OTHERWISE SPECIFIED) | U | U | 0 | SOLUTION FOR INJECTION/INFUSION | |||||||
| 119411202 | 11941120 | 4 | C | ACETAMINOPHEN. | ACETAMINOPHEN | 1 | Oral | 650 MG | U | 0 | TABLET | ||||||||
| 119411202 | 11941120 | 5 | C | ATENOLOL. | ATENOLOL | 1 | Oral | U | 0 | TABLET | |||||||||
| 119411202 | 11941120 | 6 | C | CLONIDINE. | CLONIDINE | 1 | U | 0 | |||||||||||
| 119411202 | 11941120 | 7 | C | DIPHENHYDRAMINE HYDROCHLORIDE. | DIPHENHYDRAMINE HYDROCHLORIDE | 1 | Oral | 50 MG | U | 0 | |||||||||
| 119411202 | 11941120 | 8 | C | METHYLPREDNISOLONE. | METHYLPREDNISOLONE | 1 | Intravenous (not otherwise specified) | 100 MG. INTRAVENOUS (NOT OTHERWISE SPECIFIED) | U | 0 | |||||||||
| 119411202 | 11941120 | 9 | C | PANTOPRAZOLE SODIUM. | PANTOPRAZOLE SODIUM | 1 | U | 0 | |||||||||||
| 119411202 | 11941120 | 10 | C | TRAMADOL HYDROCHLORIDE. | TRAMADOL HYDROCHLORIDE | 1 | U | 0 |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 119411202 | 11941120 | 1 | Product used for unknown indication |
| 119411202 | 11941120 | 2 | Hypertension |
| 119411202 | 11941120 | 3 | Rheumatoid arthritis |
Outcome of event
| Event ID | CASEID | OUTC COD |
|---|---|---|
| 119411202 | 11941120 | OT |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 119411202 | 11941120 | Blood pressure abnormal | |
| 119411202 | 11941120 | Blood pressure increased | |
| 119411202 | 11941120 | Cough | |
| 119411202 | 11941120 | Vaginal haemorrhage | |
| 119411202 | 11941120 | Weight increased |
Reporting Sources (this data is often not reported and may therefore be missing here)
| no results found |
Therapies reported
| no results found |