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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
126978581 | 12697858 | 1 | I | 20160824 | 20160830 | 20160830 | EXP | PHHY2016JP117489 | SANDOZ | 2.00 | MON | M | Y | 0.00000 | 20160830 | OT | JP | JP |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
126978581 | 12697858 | 1 | PS | CEFTRIAXONE. | CEFTRIAXONE | 1 | Unknown | 120 MG/KG, QD | U | 65204 | 120 | MG/KG | QD | ||||||
126978581 | 12697858 | 2 | SS | MEROPENEM. | MEROPENEM | 1 | Unknown | 140 MG/KG, QD | U | 0 | 140 | MG/KG | QD | ||||||
126978581 | 12697858 | 3 | C | DEXAMETHASONE. | DEXAMETHASONE | 1 | Unknown | 0.15 MG, UNK | U | 0 | .15 | MG |
Indications of drugs used
Event ID | CASEID | INDI DRUG SEQ | INDI PT |
---|---|---|---|
126978581 | 12697858 | 1 | Meningitis |
126978581 | 12697858 | 2 | Meningitis |
126978581 | 12697858 | 3 | Meningitis |
Outcome of event
Event ID | CASEID | OUTC COD |
---|---|---|
126978581 | 12697858 | HO |
Reactions reported
Event ID | CASEID | DRUG REC ACT | PT |
---|---|---|---|
126978581 | 12697858 | Abscess | |
126978581 | 12697858 | Condition aggravated | |
126978581 | 12697858 | Drug ineffective |
Reporting Sources (this data is often not reported and may therefore be missing here)
no results found |
Therapies reported
no results found |