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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
127787461 | 12778746 | 1 | I | 20160916 | 20160926 | 20160926 | EXP | DE-HETERO LABS LTD-1057672 | HETERO | 1.00 | MON | F | Y | 4.00000 | KG | 20160926 | DE | DE |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
127787461 | 12778746 | 1 | PS | LEVETIRACETAM. | LEVETIRACETAM | 1 | Transmammary | U | 203052 | ||||||||||
127787461 | 12778746 | 2 | SS | LAMICTAL | LAMOTRIGINE | 1 | Transmammary | U | 0 | 50 | MG |
Indications of drugs used
Event ID | CASEID | INDI DRUG SEQ | INDI PT |
---|---|---|---|
127787461 | 12778746 | 1 | Epilepsy |
Outcome of event
Event ID | CASEID | OUTC COD |
---|---|---|
127787461 | 12778746 | OT |
127787461 | 12778746 | HO |
Reactions reported
Event ID | CASEID | DRUG REC ACT | PT |
---|---|---|---|
127787461 | 12778746 | Dehydration | |
127787461 | 12778746 | Exposure during breast feeding | |
127787461 | 12778746 | Gastrooesophageal reflux disease | |
127787461 | 12778746 | Selective eating disorder | |
127787461 | 12778746 | Urinary tract infection |
Reporting Sources (this data is often not reported and may therefore be missing here)
no results found |
Therapies reported
no results found |