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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 122690075 | 12269007 | 5 | F | 20160829 | 20160414 | 20160901 | EXP | US-PFIZER INC-2016206031 | PFIZER | 67.00 | YR | F | Y | 67.00000 | KG | 20160901 | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 122690075 | 12269007 | 1 | PS | FLUCONAZOLE. | FLUCONAZOLE | 1 | Oral | 200 MG, 1X/DAY | 1222402 CZS | 19949 | 200 | MG | FILM-COATED TABLET | QD | |||||
| 122690075 | 12269007 | 2 | SS | FLUCONAZOLE. | FLUCONAZOLE | 1 | Oral | 200 MG, 1X/DAY | 19949 | 200 | MG | FILM-COATED TABLET | QD | ||||||
| 122690075 | 12269007 | 3 | SS | FLUCONAZOLE. | FLUCONAZOLE | 1 | Oral | 200 MG, 1X/DAY | 19949 | 200 | MG | FILM-COATED TABLET | QD | ||||||
| 122690075 | 12269007 | 4 | SS | FLUCONAZOLE. | FLUCONAZOLE | 1 | Oral | 200 MG, 2X/DAY | 19949 | 200 | MG | FILM-COATED TABLET | BID | ||||||
| 122690075 | 12269007 | 5 | C | ZONISAMIDE. | ZONISAMIDE | 1 | 100 MG, 4X/DAY | 0 | 100 | MG | QID | ||||||||
| 122690075 | 12269007 | 6 | C | CLONAZEPAM. | CLONAZEPAM | 1 | 0.5 | 0 | |||||||||||
| 122690075 | 12269007 | 7 | C | ARMOUR | 2 | 120 MG, 1X/DAY | 0 | 120 | MG | QD |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 122690075 | 12269007 | 1 | Fungal infection |
Outcome of event
| Event ID | CASEID | OUTC COD |
|---|---|---|
| 122690075 | 12269007 | HO |
| 122690075 | 12269007 | OT |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 122690075 | 12269007 | Alopecia | |
| 122690075 | 12269007 | Cerebrovascular accident | |
| 122690075 | 12269007 | Cough | |
| 122690075 | 12269007 | Dyspnoea | |
| 122690075 | 12269007 | Epilepsy | |
| 122690075 | 12269007 | Fear | |
| 122690075 | 12269007 | Intentional product use issue | |
| 122690075 | 12269007 | Malaise | |
| 122690075 | 12269007 | Musculoskeletal discomfort | |
| 122690075 | 12269007 | Myocardial infarction | |
| 122690075 | 12269007 | Pancreatitis | |
| 122690075 | 12269007 | Periarthritis | |
| 122690075 | 12269007 | Seizure | |
| 122690075 | 12269007 | Weight decreased |
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 |
|---|---|---|---|---|---|---|
| 122690075 | 12269007 | 1 | 2014 | 2016 | 0 | |
| 122690075 | 12269007 | 2 | 20130114 | 20140321 | 0 | |
| 122690075 | 12269007 | 3 | 20140421 | 20151230 | 0 | |
| 122690075 | 12269007 | 5 | 2000 | 0 | ||
| 122690075 | 12269007 | 6 | 2000 | 0 |