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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 123815083 | 12381508 | 3 | F | 20160830 | 20160518 | 20160907 | EXP | PHHY2016SI066142 | SANDOZ | 79.00 | YR | F | Y | 0.00000 | 20160907 | CN | COUNTRY NOT SPECIFIED | SI |
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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 123815083 | 12381508 | 1 | PS | EDEMID | FUROSEMIDE | 1 | Unknown | 40 MG, BID | U | 18569 | 40 | MG | TABLET | BID | |||||
| 123815083 | 12381508 | 2 | SS | ALOPURINOL | ALLOPURINOL | 1 | Unknown | 100 MG, UNK | U | 0 | 100 | MG | |||||||
| 123815083 | 12381508 | 3 | SS | CALCIUM | CALCIUM | 1 | Unknown | 1 G, BID | U | 0 | 1 | G | BID | ||||||
| 123815083 | 12381508 | 4 | SS | MIRCERA | METHOXY POLYETHYLENE GLYCOL-EPOETIN BETA | 1 | Subcutaneous | 100 UG, UNK | U | 0 | 100 | UG | |||||||
| 123815083 | 12381508 | 5 | SS | NOLPAZA | PANTOPRAZOLE SODIUM | 1 | Unknown | 40 MG, UNK | U | 0 | 40 | MG | |||||||
| 123815083 | 12381508 | 6 | SS | BLOXAN | METOPROLOL TARTRATE | 1 | Unknown | 100 MG, UNK | U | 0 | 100 | MG | |||||||
| 123815083 | 12381508 | 7 | SS | ALDACTONE | SPIRONOLACTONE | 1 | Unknown | 25 MG, UNK | U | 0 | 25 | MG | |||||||
| 123815083 | 12381508 | 8 | SS | CANDEA | CANDESARTAN CILEXETIL | 1 | Unknown | U | 0 | ||||||||||
| 123815083 | 12381508 | 9 | SS | ATORIS | ATORVASTATIN CALCIUM | 1 | Unknown | 20 MG, UNK | U | 0 | 20 | MG | |||||||
| 123815083 | 12381508 | 10 | SS | MAREVAN | WARFARIN SODIUM | 1 | Unknown | U | 0 |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 123815083 | 12381508 | 1 | Product used for unknown indication |
| 123815083 | 12381508 | 2 | Product used for unknown indication |
| 123815083 | 12381508 | 3 | Product used for unknown indication |
| 123815083 | 12381508 | 4 | Product used for unknown indication |
| 123815083 | 12381508 | 5 | Product used for unknown indication |
| 123815083 | 12381508 | 6 | Product used for unknown indication |
| 123815083 | 12381508 | 7 | Product used for unknown indication |
| 123815083 | 12381508 | 8 | Product used for unknown indication |
| 123815083 | 12381508 | 9 | Product used for unknown indication |
| 123815083 | 12381508 | 10 | Product used for unknown indication |
Outcome of event
| Event ID | CASEID | OUTC COD |
|---|---|---|
| 123815083 | 12381508 | HO |
| 123815083 | 12381508 | OT |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 123815083 | 12381508 | Asphyxia | |
| 123815083 | 12381508 | Condition aggravated | |
| 123815083 | 12381508 | Fluid retention |
Reporting Sources (this data is often not reported and may therefore be missing here)
| no results found |
Therapies reported
| no results found |