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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 117600582 | 11760058 | 2 | F | 20160825 | 20151120 | 20160831 | EXP | US-PFIZER INC-2015393396 | PFIZER | 0.00 | F | Y | 0.00000 | 20160831 | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 117600582 | 11760058 | 1 | PS | LYRICA | PREGABALIN | 1 | 50 MG, UNK | U | 21446 | 50 | MG | CAPSULE, HARD | |||||||
| 117600582 | 11760058 | 2 | C | PROBIOTIC | PROBIOTICS NOS | 1 | UNK | 0 |
Indications of drugs used
| no results found |
Outcome of event
| Event ID | CASEID | OUTC COD |
|---|---|---|
| 117600582 | 11760058 | OT |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 117600582 | 11760058 | Alopecia | |
| 117600582 | 11760058 | Chronic obstructive pulmonary disease | |
| 117600582 | 11760058 | Drug intolerance | |
| 117600582 | 11760058 | Emphysema | |
| 117600582 | 11760058 | Fatigue | |
| 117600582 | 11760058 | Feeling abnormal | |
| 117600582 | 11760058 | Headache | |
| 117600582 | 11760058 | Hyperhidrosis | |
| 117600582 | 11760058 | Hypersomnia | |
| 117600582 | 11760058 | Pneumonia | |
| 117600582 | 11760058 | Rash | |
| 117600582 | 11760058 | Skin disorder | |
| 117600582 | 11760058 | Weight increased |
Reporting Sources (this data is often not reported and may therefore be missing here)
| no results found |
Therapies reported
| no results found |