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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
124232403 | 12423240 | 3 | F | 20160623 | 20160601 | 20160706 | PER | PHHY2016US074854 | SANDOZ | 0.00 | F | Y | 83.90000 | KG | 20160706 | CN | COUNTRY NOT SPECIFIED | 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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
124232403 | 12423240 | 1 | SS | ELIDEL | PIMECROLIMUS | 1 | Topical | 1 IN 1 DAY | N | 8088740 | 0 | CREAM | |||||||
124232403 | 12423240 | 2 | SS | ELIDEL | PIMECROLIMUS | 1 | Topical | 2 IN 1 DAY | N | 0 | CREAM | ||||||||
124232403 | 12423240 | 3 | PS | TRIAMCINOLONE | TRIAMCINOLONE | 1 | Topical | N | 85692 | CREAM | |||||||||
124232403 | 12423240 | 4 | SS | SYNTHROID | LEVOTHYROXINE SODIUM | 1 | Oral | UNK | N | 0 | |||||||||
124232403 | 12423240 | 5 | C | ARMOUR THYROID | THYROID, PORCINE | 1 | Oral | 3 IN 1 WEEK | U | 0 | |||||||||
124232403 | 12423240 | 6 | C | PROGESTERONE. | PROGESTERONE | 1 | Topical | U | 0 | CREAM | |||||||||
124232403 | 12423240 | 7 | C | SOTALOL. | SOTALOL | 1 | Oral | U | 0 |
Indications of drugs used
Event ID | CASEID | INDI DRUG SEQ | INDI PT |
---|---|---|---|
124232403 | 12423240 | 1 | Steroid withdrawal syndrome |
124232403 | 12423240 | 3 | Product used for unknown indication |
124232403 | 12423240 | 4 | Hypothyroidism |
124232403 | 12423240 | 5 | Product used for unknown indication |
124232403 | 12423240 | 6 | Product used for unknown indication |
124232403 | 12423240 | 7 | Product used for unknown indication |
Outcome of event
no results found |
Reactions reported
Event ID | CASEID | DRUG REC ACT | PT |
---|---|---|---|
124232403 | 12423240 | Abdominal pain | |
124232403 | 12423240 | Asthenia | |
124232403 | 12423240 | Infection | |
124232403 | 12423240 | Off label use | |
124232403 | 12423240 | Rectal haemorrhage | |
124232403 | 12423240 | Vaginal haemorrhage | |
124232403 | 12423240 | 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 |
---|---|---|---|---|---|---|
124232403 | 12423240 | 1 | 201603 | 0 | ||
124232403 | 12423240 | 2 | 201603 | 2016 | 0 |