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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
127178752 | 12717875 | 2 | F | 20160916 | 20160906 | 20160926 | EXP | US-MYLANLABS-2016M1037458 | MYLAN | MIESNER AR, AUSMAN M, DAGRAEDT B, ZIEMINSKI J. PROBABLE DRUG INTERACTION BETWEEN EVEROLIMUS AND CLARITHROMYCIN. ANN-PHARMACOTHER 2016;50(8):689-690. | 0.00 | Y | 0.00000 | 20160926 | PH | 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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
127178752 | 12717875 | 1 | PS | FUROSEMIDE. | FUROSEMIDE | 1 | U | U | 18487 | ||||||||||
127178752 | 12717875 | 2 | I | CLARITHROMYCIN. | CLARITHROMYCIN | 1 | Oral | Y | U | 0 | 500 | MG | BID | ||||||
127178752 | 12717875 | 3 | I | EVEROLIMUS | EVEROLIMUS | 1 | Oral | 10MG DAILY | Y | 0 | |||||||||
127178752 | 12717875 | 4 | C | AMOXICILLIN. | AMOXICILLIN | 1 | Oral | Y | 0 | 500 | MG | BID | |||||||
127178752 | 12717875 | 5 | C | OMEPRAZOLE. | OMEPRAZOLE | 1 | Oral | 40MG DAILY | Y | 0 | |||||||||
127178752 | 12717875 | 6 | C | LEVOTHYROXINE SODIUM. | LEVOTHYROXINE SODIUM | 1 | Oral | 200MICROG DAILY | D | 0 | |||||||||
127178752 | 12717875 | 7 | C | METOPROLOL SUCCINATE. | METOPROLOL SUCCINATE | 1 | Oral | 25MG | D | 0 |
Indications of drugs used
Event ID | CASEID | INDI DRUG SEQ | INDI PT |
---|---|---|---|
127178752 | 12717875 | 1 | Product used for unknown indication |
127178752 | 12717875 | 2 | Helicobacter infection |
127178752 | 12717875 | 3 | Product used for unknown indication |
127178752 | 12717875 | 4 | Helicobacter infection |
127178752 | 12717875 | 5 | Helicobacter infection |
127178752 | 12717875 | 6 | Product used for unknown indication |
127178752 | 12717875 | 7 | Product used for unknown indication |
Outcome of event
Event ID | CASEID | OUTC COD |
---|---|---|
127178752 | 12717875 | HO |
Reactions reported
Event ID | CASEID | DRUG REC ACT | PT |
---|---|---|---|
127178752 | 12717875 | Acute kidney injury | |
127178752 | 12717875 | Drug interaction | |
127178752 | 12717875 | Hyperkalaemia |
Reporting Sources (this data is often not reported and may therefore be missing here)
no results found |
Therapies reported
no results found |