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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 127365641 | 12736564 | 1 | I | 20150821 | 20160905 | 20160913 | 20160913 | EXP | SE-MPA-2016-004982 | PHHY2016SE122636 | NOVARTIS | 85.00 | YR | F | Y | 0.00000 | 20160913 | OT | SE | SE |
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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 127365641 | 12736564 | 1 | PS | ACLASTA | ZOLEDRONIC ACID | 1 | Unknown | 5 MG, UNK | 21817 | 5 | MG | SOLUTION FOR INJECTION | |||||||
| 127365641 | 12736564 | 2 | C | KALCIPOS-D | CALCIUM CARBONATECHOLECALCIFEROL | 1 | Unknown | 500 MG/ 800 IE, UNK | U | 0 | 500 | MG | CHEWABLE TABLET | ||||||
| 127365641 | 12736564 | 3 | C | WARAN | WARFARIN SODIUM | 1 | Unknown | 2.5 MG, UNK | U | 0 | 2.5 | MG | TABLET | ||||||
| 127365641 | 12736564 | 4 | C | FURIX | FUROSEMIDE | 1 | Unknown | 40 MG, UNK | U | 0 | 40 | MG | TABLET | ||||||
| 127365641 | 12736564 | 5 | C | ENALAPRIL SANDOZ | ENALAPRIL | 1 | Unknown | 10 MG, UNK | U | 0 | 10 | MG | TABLET | ||||||
| 127365641 | 12736564 | 6 | C | CORTIMYK | 2 | Unknown | 20 MG/G | U | 0 | ||||||||||
| 127365641 | 12736564 | 7 | C | PROPYLESS | 2 | Unknown | 200 MG, UNK | U | 0 | 200 | MG | EMULSION | |||||||
| 127365641 | 12736564 | 8 | C | BETNOVAT | BETAMETHASONE | 1 | Unknown | 1 MG/ML, UNK | U | 0 | LOTION | ||||||||
| 127365641 | 12736564 | 9 | C | SELSUN | SELENIUM SULFIDE | 1 | Unknown | 25 MG/ML, UNK | U | 0 | SHAMPOO | ||||||||
| 127365641 | 12736564 | 10 | C | PROTOPIC | TACROLIMUS | 1 | Unknown | 0.1 %, UNK | U | 0 | .1 | PCT | |||||||
| 127365641 | 12736564 | 11 | C | SIFROL | PRAMIPEXOLE | 1 | Unknown | 0.18 MG, UNK | U | 0 | .18 | MG | TABLET |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 127365641 | 12736564 | 1 | Osteoporosis |
| 127365641 | 12736564 | 2 | Product used for unknown indication |
| 127365641 | 12736564 | 3 | Product used for unknown indication |
| 127365641 | 12736564 | 4 | Product used for unknown indication |
| 127365641 | 12736564 | 5 | Product used for unknown indication |
| 127365641 | 12736564 | 6 | Product used for unknown indication |
| 127365641 | 12736564 | 7 | Product used for unknown indication |
| 127365641 | 12736564 | 8 | Product used for unknown indication |
| 127365641 | 12736564 | 9 | Product used for unknown indication |
| 127365641 | 12736564 | 10 | Product used for unknown indication |
| 127365641 | 12736564 | 11 | Product used for unknown indication |
Outcome of event
| Event ID | CASEID | OUTC COD |
|---|---|---|
| 127365641 | 12736564 | DS |
| 127365641 | 12736564 | HO |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 127365641 | 12736564 | Fatigue | |
| 127365641 | 12736564 | Myalgia | |
| 127365641 | 12736564 | Pruritus | |
| 127365641 | 12736564 | Pyrexia | |
| 127365641 | 12736564 | Rash | |
| 127365641 | 12736564 | Red blood cell sedimentation rate increased |
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 |
|---|---|---|---|---|---|---|
| 127365641 | 12736564 | 1 | 20150821 | 20150821 | 0 |