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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
127115232 | 12711523 | 2 | F | 20160304 | 20160902 | 20160902 | 20160912 | PER | US-PFIZER INC-2016139926 | PFIZER | 2.00 | YR | F | Y | 13.00000 | KG | 20160912 | CN | 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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
127115232 | 12711523 | 1 | PS | RAPAMUNE | SIROLIMUS | 1 | Oral | 0.75 MG, 1X/DAY (FOR 1 WEEK) | 21083 | .75 | MG | ORAL SOLUTION | QD | ||||||
127115232 | 12711523 | 2 | SS | RAPAMUNE | SIROLIMUS | 1 | Oral | 1 ML, 1X/DAY | VSFK13122902 | 21083 | 1 | ML | ORAL SOLUTION | QD | |||||
127115232 | 12711523 | 3 | SS | RAPAMUNE | SIROLIMUS | 1 | Oral | 2 ML, DAILY | 21083 | 2 | ML | ORAL SOLUTION | |||||||
127115232 | 12711523 | 4 | C | PHENOBARBITAL. | PHENOBARBITAL | 1 | Oral | 8.5 ML, 2X/DAY | 0 | 8.5 | ML | BID | |||||||
127115232 | 12711523 | 5 | C | TOPAMAX | TOPIRAMATE | 1 | Oral | 75 MG, 2X/DAY | 0 | 75 | MG | TABLET | BID | ||||||
127115232 | 12711523 | 6 | C | OXCARBAZEPINE. | OXCARBAZEPINE | 1 | Oral | 2.5 ML, 2X/DAY | 0 | 2.5 | ML | BID |
Indications of drugs used
Event ID | CASEID | INDI DRUG SEQ | INDI PT |
---|---|---|---|
127115232 | 12711523 | 1 | Epilepsy |
127115232 | 12711523 | 2 | Renal artery dissection |
127115232 | 12711523 | 4 | Seizure |
127115232 | 12711523 | 5 | Seizure |
127115232 | 12711523 | 6 | Seizure |
Outcome of event
no results found |
Reactions reported
Event ID | CASEID | DRUG REC ACT | PT |
---|---|---|---|
127115232 | 12711523 | Drug level decreased | |
127115232 | 12711523 | Product use issue |
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 |
---|---|---|---|---|---|---|
127115232 | 12711523 | 1 | 20160304 | 0 | ||
127115232 | 12711523 | 2 | 201602 | 0 | ||
127115232 | 12711523 | 3 | 20160901 | 0 | ||
127115232 | 12711523 | 6 | 201511 | 0 |