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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
126209242 | 12620924 | 2 | F | 2012 | 20160816 | 20160804 | 20160829 | EXP | BE-SUN PHARMACEUTICAL INDUSTRIES LTD-2016R1-121466 | RANBAXY | 55.00 | YR | M | Y | 0.00000 | 20160829 | OT | GB | BE |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
126209242 | 12620924 | 1 | PS | CITALOPRAM | CITALOPRAM HYDROBROMIDE | 1 | Unknown | UNK | 77032 | ||||||||||
126209242 | 12620924 | 2 | I | FENTANYL. | FENTANYL | 1 | Transdermal | UNK | 0 | ||||||||||
126209242 | 12620924 | 3 | I | METHYLPREDNISOLONE. | METHYLPREDNISOLONE | 1 | Unknown | 4 MG, DAILY | 0 | 4 | MG | ||||||||
126209242 | 12620924 | 4 | I | METHYLPREDNISOLONE. | METHYLPREDNISOLONE | 1 | Intravenous (not otherwise specified) | UNK | 0 | ||||||||||
126209242 | 12620924 | 5 | I | METHYLPREDNISOLONE. | METHYLPREDNISOLONE | 1 | 0 | ||||||||||||
126209242 | 12620924 | 6 | I | MYCOPHENOLATE MOFETIL. | MYCOPHENOLATE MOFETIL | 1 | Unknown | 500 MG, BID | U | 0 | 500 | MG | Q12H | ||||||
126209242 | 12620924 | 7 | I | TACROLIMUS. | TACROLIMUS | 1 | Unknown | 0.5 MG, BID | U | 0 | .5 | MG | Q12H | ||||||
126209242 | 12620924 | 8 | C | CIPROFLOXACIN. | CIPROFLOXACIN | 1 | Oral | 500 MG, BID | U | 0 | 500 | MG | Q12H | ||||||
126209242 | 12620924 | 9 | C | METFORMIN | METFORMIN HYDROCHLORIDE | 1 | Oral | 500 MG, BID | U | 0 | 500 | MG | Q12H | ||||||
126209242 | 12620924 | 10 | C | SULFAMETHOXAZOLE-TRIMETHOPRIM (SMZ) | SULFAMETHOXAZOLETRIMETHOPRIM | 1 | Oral | UNK, BID | U | 0 | Q12H | ||||||||
126209242 | 12620924 | 11 | C | ZOLEDRONIC ACID | ZOLEDRONIC ACID | 1 | Unknown | UNK | U | 0 |
Indications of drugs used
Event ID | CASEID | INDI DRUG SEQ | INDI PT |
---|---|---|---|
126209242 | 12620924 | 1 | Product used for unknown indication |
126209242 | 12620924 | 2 | Thoracic vertebral fracture |
126209242 | 12620924 | 3 | Immunosuppression |
126209242 | 12620924 | 4 | Immunosuppression |
126209242 | 12620924 | 5 | Transplant rejection |
126209242 | 12620924 | 6 | Immunosuppression |
126209242 | 12620924 | 7 | Immunosuppression |
126209242 | 12620924 | 8 | Sinusitis bacterial |
126209242 | 12620924 | 9 | Glucose tolerance impaired |
126209242 | 12620924 | 10 | Pseudomonas infection |
126209242 | 12620924 | 11 | Thoracic vertebral fracture |
Outcome of event
Event ID | CASEID | OUTC COD |
---|---|---|
126209242 | 12620924 | OT |
Reactions reported
Event ID | CASEID | DRUG REC ACT | PT |
---|---|---|---|
126209242 | 12620924 | Drug interaction | |
126209242 | 12620924 | Hyponatraemia | |
126209242 | 12620924 | Stupor |
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 |
---|---|---|---|---|---|---|
126209242 | 12620924 | 1 | 2012 | 2012 | 0 | |
126209242 | 12620924 | 2 | 2012 | 2012 | 0 | |
126209242 | 12620924 | 8 | 2012 | 0 | ||
126209242 | 12620924 | 9 | 2012 | 0 | ||
126209242 | 12620924 | 11 | 2012 | 0 |