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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 126023691 | 12602369 | 1 | I | 2015 | 20151016 | 20160728 | 20160728 | PER | US-PFIZER INC-3049533 | PFIZER | 31.00 | YR | M | Y | 64.60000 | KG | 20160728 | OT | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 126023691 | 12602369 | 1 | PS | CEFEPIME HCL | CEFEPIME HYDROCHLORIDE | 1 | Intravenous (not otherwise specified) | UNK | U | UNK | 50679 | ||||||||
| 126023691 | 12602369 | 2 | SS | CEFOXITIN SODIUM | CEFOXITIN SODIUM | 1 | Intravenous (not otherwise specified) | UNK | UNK | 65313 | POWDER FOR INJECTION | ||||||||
| 126023691 | 12602369 | 3 | SS | VANCOMYCIN HCL | VANCOMYCIN HYDROCHLORIDE | 1 | Intravenous (not otherwise specified) | UNK | U | UNK | 62911 | ||||||||
| 126023691 | 12602369 | 4 | SS | MINOCYCLINE | MINOCYCLINEMINOCYCLINE HYDROCHLORIDE | 1 | Oral | UNK | 0 | ||||||||||
| 126023691 | 12602369 | 5 | SS | BIAXIN | CLARITHROMYCIN | 1 | Oral | UNK | UNK | 0 | |||||||||
| 126023691 | 12602369 | 6 | SS | MINOCYCLINE | MINOCYCLINEMINOCYCLINE HYDROCHLORIDE | 1 | Oral | UNK | UNK | 0 | |||||||||
| 126023691 | 12602369 | 7 | SS | VANCOMYCIN | VANCOMYCIN | 1 | Intravenous (not otherwise specified) | UNK | U | 0 | |||||||||
| 126023691 | 12602369 | 8 | SS | CEFEPIME | CEFEPIME HYDROCHLORIDE | 1 | Intravenous (not otherwise specified) | UNK | U | 0 |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 126023691 | 12602369 | 1 | Product used for unknown indication |
| 126023691 | 12602369 | 2 | Product used for unknown indication |
| 126023691 | 12602369 | 3 | Product used for unknown indication |
| 126023691 | 12602369 | 5 | Product used for unknown indication |
| 126023691 | 12602369 | 6 | Product used for unknown indication |
Outcome of event
| Event ID | CASEID | OUTC COD |
|---|---|---|
| 126023691 | 12602369 | OT |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 126023691 | 12602369 | Abdominal discomfort | |
| 126023691 | 12602369 | Drug resistance | |
| 126023691 | 12602369 | Thrombocytopenia |
Reporting Sources (this data is often not reported and may therefore be missing here)
| no results found |
Therapies reported
| no results found |