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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 125365351 | 12536535 | 1 | I | 2016 | 20160613 | 20160707 | 20160707 | PER | US-PFIZER INC-2016299530 | PFIZER | 74.00 | YR | M | Y | 54.00000 | KG | 20160707 | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 125365351 | 12536535 | 1 | PS | GABAPENTIN. | GABAPENTIN | 1 | Oral | 300 MG, 3X/DAY | 20235 | 300 | MG | CAPSULE, HARD | TID | ||||||
| 125365351 | 12536535 | 2 | SS | GABAPENTIN. | GABAPENTIN | 1 | Oral | 300 MG, 2X/DAY, 'AT BEDTIME' | 20235 | 300 | MG | CAPSULE, HARD | BID | ||||||
| 125365351 | 12536535 | 3 | C | LEXAPRO | ESCITALOPRAM OXALATE | 1 | 20 MG, 1X/DAY | 0 | 20 | MG | QD | ||||||||
| 125365351 | 12536535 | 4 | C | LEXAPRO | ESCITALOPRAM OXALATE | 1 | 0 | ||||||||||||
| 125365351 | 12536535 | 5 | C | PROPANOLOL /00030001/ | PROPRANOLOL HYDROCHLORIDE | 1 | 40 MG, 3X/DAY | 0 | 40 | MG | TID | ||||||||
| 125365351 | 12536535 | 6 | C | LIPITOR | ATORVASTATIN CALCIUM | 1 | 40 MG, 1X/DAY | 0 | 40 | MG | QD |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 125365351 | 12536535 | 1 | Pain |
| 125365351 | 12536535 | 3 | Depression |
| 125365351 | 12536535 | 4 | Anxiety |
| 125365351 | 12536535 | 5 | Migraine prophylaxis |
| 125365351 | 12536535 | 6 | Blood cholesterol increased |
Outcome of event
| no results found |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 125365351 | 12536535 | Condition aggravated | |
| 125365351 | 12536535 | Head discomfort | |
| 125365351 | 12536535 | Headache | |
| 125365351 | 12536535 | 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 |
|---|---|---|---|---|---|---|
| 125365351 | 12536535 | 1 | 20160315 | 0 | ||
| 125365351 | 12536535 | 3 | 201308 | 0 | ||
| 125365351 | 12536535 | 6 | 1998 | 0 |