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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
123926702 | 12392670 | 2 | F | 20160622 | 20160523 | 20160706 | PER | PHEH2016US011934 | NOVARTIS | 0.00 | F | Y | 0.00000 | 20160624 | 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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
123926702 | 12392670 | 1 | PS | DIOVAN HCT | HYDROCHLOROTHIAZIDEVALSARTAN | 1 | Oral | 1 DF (160 MG VALSARTAN, 25 MG HCT), UNK | U | F0539 | 20818 | 1 | DF | ||||||
123926702 | 12392670 | 2 | SS | VALSARTAN. | VALSARTAN | 1 | Unknown | U | 0 | ||||||||||
123926702 | 12392670 | 3 | C | OGEN | ESTROPIPATE | 1 | Unknown | 0.625 OT, UNK | U | 0 | |||||||||
123926702 | 12392670 | 4 | C | PANTOPRAZOLE | PANTOPRAZOLE SODIUM | 1 | Unknown | 40 MG, QD | U | 0 | 40 | MG | QD | ||||||
123926702 | 12392670 | 5 | C | HYDROXYZINE HCL | HYDROXYZINE HYDROCHLORIDE | 1 | Unknown | 10 MG, BID | U | 0 | 10 | MG | BID | ||||||
123926702 | 12392670 | 6 | C | POTASSIUM CHLORIDE. | POTASSIUM CHLORIDE | 1 | Unknown | 10 MEQ, UNK | U | 0 | 10 | MEQ | EXTENDED RELEASE CAPSULES | ||||||
123926702 | 12392670 | 7 | C | ELAVIL | AMITRIPTYLINE HYDROCHLORIDE | 1 | Unknown | 75 MG, UNK | U | 0 | 75 | MG | |||||||
123926702 | 12392670 | 8 | C | TYLENOL EXTRA STRENGTH | ACETAMINOPHEN | 1 | Unknown | U | 0 | ||||||||||
123926702 | 12392670 | 9 | C | DIAZEPAM. | DIAZEPAM | 1 | Unknown | 10 MG, PRN | U | 0 | 10 | MG |
Indications of drugs used
Event ID | CASEID | INDI DRUG SEQ | INDI PT |
---|---|---|---|
123926702 | 12392670 | 1 | Product used for unknown indication |
123926702 | 12392670 | 2 | Product used for unknown indication |
123926702 | 12392670 | 3 | Product used for unknown indication |
123926702 | 12392670 | 4 | Product used for unknown indication |
123926702 | 12392670 | 5 | Hypersensitivity |
123926702 | 12392670 | 6 | Product used for unknown indication |
123926702 | 12392670 | 7 | Product used for unknown indication |
123926702 | 12392670 | 8 | Product used for unknown indication |
123926702 | 12392670 | 9 | Muscle spasms |
Outcome of event
no results found |
Reactions reported
Event ID | CASEID | DRUG REC ACT | PT |
---|---|---|---|
123926702 | 12392670 | Blood pressure inadequately controlled | |
123926702 | 12392670 | Micturition disorder | |
123926702 | 12392670 | Tremor | |
123926702 | 12392670 | Weight increased |
Reporting Sources (this data is often not reported and may therefore be missing here)
no results found |
Therapies reported
no results found |