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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
126006483 | 12600648 | 3 | F | 201307 | 20160830 | 20160727 | 20160906 | EXP | JP-SUCAMPO PHARMACEUTICALS, INC.-SPI201600801 | SUCAMPO | 70.86 | YR | M | Y | 0.00000 | 20160906 | PH | JP | JP |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
126006483 | 12600648 | 1 | PS | AMITIZA | LUBIPROSTONE | 1 | Oral | 24 MCG, QD | Y | 21908 | 24 | UG | CAPSULE | QD | |||||
126006483 | 12600648 | 2 | SS | Magmitt | MAGNESIUM OXIDE | 1 | Oral | UNK | 0 | ORAL DRUG UNSPECIFIED FORM | |||||||||
126006483 | 12600648 | 3 | C | Cetilo | SENNA LEAF | 1 | Oral | UNK | 0 | TABLET | |||||||||
126006483 | 12600648 | 4 | C | LIPITOR | ATORVASTATIN CALCIUM | 1 | Oral | UNK | 0 | TABLET | |||||||||
126006483 | 12600648 | 5 | C | Laxoberon | SODIUM PICOSULFATE | 1 | Oral | UNK | 0 | ORAL DRUG UNSPECIFIED FORM | |||||||||
126006483 | 12600648 | 6 | C | Unknown | UNSPECIFIED INGREDIENT | 1 | Oral | UNK | 0 | ORAL DRUG UNSPECIFIED FORM | |||||||||
126006483 | 12600648 | 7 | C | Unknown | UNSPECIFIED INGREDIENT | 1 | UNK | 0 |
Indications of drugs used
Event ID | CASEID | INDI DRUG SEQ | INDI PT |
---|---|---|---|
126006483 | 12600648 | 1 | Constipation |
126006483 | 12600648 | 2 | Constipation |
126006483 | 12600648 | 3 | Constipation |
126006483 | 12600648 | 4 | Hyperlipidaemia |
Outcome of event
Event ID | CASEID | OUTC COD |
---|---|---|
126006483 | 12600648 | OT |
Reactions reported
Event ID | CASEID | DRUG REC ACT | PT |
---|---|---|---|
126006483 | 12600648 | Inappropriate schedule of drug administration | |
126006483 | 12600648 | Loss of consciousness |
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 |
---|---|---|---|---|---|---|
126006483 | 12600648 | 1 | 20130723 | 201307 | 0 | |
126006483 | 12600648 | 2 | 20130723 | 20150906 | 0 |