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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
123133162 | 12313316 | 2 | F | 20160924 | 20160428 | 20160926 | PER | US-PFIZER INC-2016200612 | PFIZER | 71.00 | YR | F | Y | 0.00000 | 20160926 | 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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
123133162 | 12313316 | 1 | PS | ALAVERT ALLERGY | LORATADINE | 1 | Oral | 10MG, DISINTEGRATING TABLET, ONCE A DAY | K00414 | 21375 | 10 | MG | ORODISPERSIBLE TABLET | QD | |||||
123133162 | 12313316 | 2 | SS | ALAVERT ALLERGY | LORATADINE | 1 | 21375 | ORODISPERSIBLE TABLET | |||||||||||
123133162 | 12313316 | 3 | SS | ALAVERT ALLERGY | LORATADINE | 1 | 21375 | ORODISPERSIBLE TABLET | |||||||||||
123133162 | 12313316 | 4 | SS | ALAVERT ALLERGY | LORATADINE | 1 | 21375 | ORODISPERSIBLE TABLET | |||||||||||
123133162 | 12313316 | 5 | SS | IBUPROFEN. | IBUPROFEN | 1 | Oral | 1 DF, DAILY | 18989 | 1 | DF | TABLET | |||||||
123133162 | 12313316 | 6 | SS | BENADRYL | DIPHENHYDRAMINE HYDROCHLORIDE | 1 | UNK | U | 0 | ||||||||||
123133162 | 12313316 | 7 | SS | LETROZOLE. | LETROZOLE | 1 | Oral | 2.5 MG, DAILY | 0 | 2.5 | MG | TABLET |
Indications of drugs used
Event ID | CASEID | INDI DRUG SEQ | INDI PT |
---|---|---|---|
123133162 | 12313316 | 1 | Lacrimation increased |
123133162 | 12313316 | 2 | Rhinorrhoea |
123133162 | 12313316 | 3 | Eye pruritus |
123133162 | 12313316 | 4 | Drug reaction with eosinophilia and systemic symptoms |
123133162 | 12313316 | 7 | Breast cancer |
Outcome of event
no results found |
Reactions reported
Event ID | CASEID | DRUG REC ACT | PT |
---|---|---|---|
123133162 | 12313316 | Condition aggravated | |
123133162 | 12313316 | Drug ineffective | |
123133162 | 12313316 | Myalgia |
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 |
---|---|---|---|---|---|---|
123133162 | 12313316 | 1 | 2015 | 0 | ||
123133162 | 12313316 | 7 | 2011 | 0 |