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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 127770842 | 12777084 | 2 | F | 20160918 | 20160921 | 20160923 | 20160927 | PER | US-JNJFOC-20160920803 | JOHNSON AND JOHNSON | 0.00 | F | Y | 0.00000 | 20160927 | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 127770842 | 12777084 | 1 | PS | ZYRTEC | CETIRIZINE HYDROCHLORIDE | 1 | Oral | U | U | 449048 | 19835 | TABLET | |||||||
| 127770842 | 12777084 | 2 | SS | ZYRTEC | CETIRIZINE HYDROCHLORIDE | 1 | Oral | FOR ABOUT A WEEK | U | U | 449048 | 19835 | 10 | MG | TABLET | QD | |||
| 127770842 | 12777084 | 3 | C | INSULIN | INSULIN NOS | 1 | Unknown | D | 0 | UNSPECIFIED | |||||||||
| 127770842 | 12777084 | 4 | C | IBRANCE | PALBOCICLIB | 1 | Unknown | D | 0 | UNSPECIFIED | |||||||||
| 127770842 | 12777084 | 5 | C | DESMOPRESSIN | DESMOPRESSIN | 1 | Unknown | D | 0 | UNSPECIFIED | |||||||||
| 127770842 | 12777084 | 6 | C | DESMOPRESSIN | DESMOPRESSIN | 1 | Unknown | D | 0 | UNSPECIFIED | |||||||||
| 127770842 | 12777084 | 7 | C | CLARITIN | LORATADINE | 1 | Unknown | FOR ABOUT A WEEK | D | 0 | UNSPECIFIED |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 127770842 | 12777084 | 2 | Seasonal allergy |
| 127770842 | 12777084 | 3 | Blood glucose increased |
| 127770842 | 12777084 | 4 | Breast cancer |
| 127770842 | 12777084 | 5 | Diabetes insipidus |
| 127770842 | 12777084 | 6 | Fluid replacement |
| 127770842 | 12777084 | 7 | Product used for unknown indication |
Outcome of event
| no results found |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 127770842 | 12777084 | Incorrect dose administered |
Reporting Sources (this data is often not reported and may therefore be missing here)
| no results found |
Therapies reported
| no results found |