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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 81573375 | 8157337 | 5 | F | 2000 | 20160712 | 20110927 | 20160718 | EXP | US-PFIZER INC-2011169440 | PFIZER | 54.00 | YR | F | Y | 76.64000 | KG | 20160718 | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 81573375 | 8157337 | 1 | PS | DILANTIN | PHENYTOIN | 1 | Oral | 100 MG, 1X/DAY | 84349 | 100 | MG | CAPSULE, HARD | QD | ||||||
| 81573375 | 8157337 | 2 | I | DILANTIN | PHENYTOIN | 1 | Oral | 160MG IN THE MORNING AND 200MG IN THE NIGHT | 84349 | CAPSULE, HARD | BID | ||||||||
| 81573375 | 8157337 | 3 | I | DILANTIN | PHENYTOIN | 1 | Oral | 100MG ONE DURING THE DAY AND ONE AT NIGHT | 84349 | 100 | MG | CAPSULE, HARD | BID | ||||||
| 81573375 | 8157337 | 4 | I | DILANTIN | PHENYTOIN | 1 | Oral | 60 MG, 1X/DAY (30 MG 2 AT 07:00 AM) | 84349 | 60 | MG | CAPSULE, HARD | QD | ||||||
| 81573375 | 8157337 | 5 | I | DILANTIN | PHENYTOIN | 1 | Oral | 2-100 MG AT 07:00 PM 100 MG 2 AT 07:00 A.M | 84349 | CAPSULE, HARD | |||||||||
| 81573375 | 8157337 | 6 | I | CIPROFLOXACIN HCL | CIPROFLOXACIN HYDROCHLORIDE | 1 | 280 MG, 2X/DAY | U | 77245 | 280 | MG | BID | |||||||
| 81573375 | 8157337 | 7 | I | SULFAMETHOXAZOLE-TRIMETHOPRIM (SMZ) | SULFAMETHOXAZOLETRIMETHOPRIM | 1 | UNK | U | 0 | ||||||||||
| 81573375 | 8157337 | 8 | SS | KEPPRA | LEVETIRACETAM | 1 | 500 MG, 2X/DAY | U | 0 | 500 | MG | BID | |||||||
| 81573375 | 8157337 | 9 | SS | KEPPRA | LEVETIRACETAM | 1 | 500 (07:00 AM + 07: 00 PM) | U | 0 | BID | |||||||||
| 81573375 | 8157337 | 10 | SS | PHENOBARBITAL. | PHENOBARBITAL | 1 | 90 MG, DAILY ((30 MG + 60 MG) AT 07:00 PM) | 0 | 90 | MG | |||||||||
| 81573375 | 8157337 | 11 | SS | PHENOBARBITAL. | PHENOBARBITAL | 1 | 30 MG, UNK | 0 | 30 | MG |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 81573375 | 8157337 | 1 | Generalised tonic-clonic seizure |
| 81573375 | 8157337 | 2 | Petit mal epilepsy |
| 81573375 | 8157337 | 3 | Seizure |
| 81573375 | 8157337 | 6 | Cystitis |
| 81573375 | 8157337 | 7 | Cystitis |
| 81573375 | 8157337 | 8 | Seizure |
| 81573375 | 8157337 | 10 | Seizure |
Outcome of event
| Event ID | CASEID | OUTC COD |
|---|---|---|
| 81573375 | 8157337 | OT |
| 81573375 | 8157337 | HO |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 81573375 | 8157337 | Condition aggravated | |
| 81573375 | 8157337 | Cystitis | |
| 81573375 | 8157337 | Drug ineffective | |
| 81573375 | 8157337 | Drug interaction | |
| 81573375 | 8157337 | Feeling abnormal | |
| 81573375 | 8157337 | Headache | |
| 81573375 | 8157337 | Insomnia | |
| 81573375 | 8157337 | Seizure |
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 |
|---|---|---|---|---|---|---|
| 81573375 | 8157337 | 1 | 1964 | 0 |