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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
96529332 | 9652933 | 2 | F | 20160923 | 20131029 | 20160927 | PER | US-PFIZER INC-2013304495 | PFIZER | 60.00 | YR | F | Y | 0.00000 | 20160927 | MD | 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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
96529332 | 9652933 | 1 | PS | CLEOCIN | CLINDAMYCIN PHOSPHATE | 1 | UNK | U | 50441 | ||||||||||
96529332 | 9652933 | 2 | SS | CLINDAMYCIN HCL | CLINDAMYCIN HYDROCHLORIDE | 1 | UNK | U | 50162 | CAPSULE, HARD | |||||||||
96529332 | 9652933 | 3 | SS | BUTORPHANOL TARTRATE. | BUTORPHANOL TARTRATE | 1 | UNK | U | 74626 | ||||||||||
96529332 | 9652933 | 4 | SS | CODEINE | CODEINE | 1 | UNK | U | 0 | ||||||||||
96529332 | 9652933 | 5 | SS | STADOL | BUTORPHANOL TARTRATE | 1 | UNK | U | 0 | ||||||||||
96529332 | 9652933 | 6 | SS | FLEXERIL | CYCLOBENZAPRINE HYDROCHLORIDE | 1 | UNK | U | 0 | ||||||||||
96529332 | 9652933 | 7 | SS | VALTREX | VALACYCLOVIR HYDROCHLORIDE | 1 | UNK | U | 0 | ||||||||||
96529332 | 9652933 | 8 | SS | VIOXX | ROFECOXIB | 1 | UNK | U | 0 |
Indications of drugs used
no results found |
Outcome of event
no results found |
Reactions reported
Event ID | CASEID | DRUG REC ACT | PT |
---|---|---|---|
96529332 | 9652933 | Drug hypersensitivity |
Reporting Sources (this data is often not reported and may therefore be missing here)
no results found |
Therapies reported
no results found |