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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
125307591 | 12530759 | 1 | I | 20160608 | 20160706 | 20160706 | PER | US-PFIZER INC-2016295132 | PFIZER | 0.00 | Y | 0.00000 | 20160706 | 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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
125307591 | 12530759 | 1 | PS | NORVASC | AMLODIPINE BESYLATE | 1 | UNK | U | 19787 | FILM-COATED TABLET | |||||||||
125307591 | 12530759 | 2 | SS | NEXIUM | ESOMEPRAZOLE MAGNESIUM | 1 | UNK | U | 0 | ||||||||||
125307591 | 12530759 | 3 | SS | METOPROLOL TARTRATE. | METOPROLOL TARTRATE | 1 | UNK | U | 74133 | ||||||||||
125307591 | 12530759 | 4 | SS | ONDANSETRON | ONDANSETRON | 1 | UNK | U | 77548 | SOLUTION FOR INJECTION | |||||||||
125307591 | 12530759 | 5 | SS | HYDROCHLOROTHIAZIDE. | HYDROCHLOROTHIAZIDE | 1 | UNK | U | 0 | ||||||||||
125307591 | 12530759 | 6 | SS | PREZISTA | DARUNAVIR ETHANOLATE | 1 | UNK | U | 0 | ||||||||||
125307591 | 12530759 | 7 | SS | ALBUTEROL. | ALBUTEROL | 1 | UNK | U | 0 | INHALATION VAPOUR | |||||||||
125307591 | 12530759 | 8 | SS | BENZTROPINE | BENZTROPINE | 1 | UNK | U | 0 | ||||||||||
125307591 | 12530759 | 9 | SS | DIVALPROEX SODIUM. | DIVALPROEX SODIUM | 1 | UNK | U | 0 | ||||||||||
125307591 | 12530759 | 10 | SS | RISPERIDONE. | RISPERIDONE | 1 | UNK | U | 0 | ||||||||||
125307591 | 12530759 | 11 | SS | TIVICAY | DOLUTEGRAVIR SODIUM | 1 | UNK | U | 0 | ||||||||||
125307591 | 12530759 | 12 | SS | LISINOPRIL. | LISINOPRIL | 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 |
---|---|---|---|
125307591 | 12530759 | Drug hypersensitivity |
Reporting Sources (this data is often not reported and may therefore be missing here)
no results found |
Therapies reported
no results found |