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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
127223551 | 12722355 | 1 | I | 20160803 | 20160907 | 20160907 | PER | US-AMNEAL PHARMACEUTICALS-2016AMN00430 | AMNEAL | 0.00 | F | Y | 70.30000 | KG | 20160907 | 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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
127223551 | 12722355 | 1 | PS | LIDOCAINE. | LIDOCAINE | 1 | Topical | 5 %, 3X/DAY | N | 09186145A | 206297 | 5 | PCT | OINTMENT | TID | ||||
127223551 | 12722355 | 2 | C | chewable multiviatmin | 2 | U | 0 | ||||||||||||
127223551 | 12722355 | 3 | C | chewable calcium citrate | 2 | U | 0 |
Indications of drugs used
Event ID | CASEID | INDI DRUG SEQ | INDI PT |
---|---|---|---|
127223551 | 12722355 | 1 | Tendon pain |
Outcome of event
no results found |
Reactions reported
Event ID | CASEID | DRUG REC ACT | PT |
---|---|---|---|
127223551 | 12722355 | Drug ineffective |
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 |
---|---|---|---|---|---|---|
127223551 | 12722355 | 1 | 20160720 | 20160723 | 0 |