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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
127358181 | 12735818 | 1 | I | 20160721 | 20160913 | 20160913 | PER | US-JNJFOC-20160718884 | JANSSEN | 78.00 | YR | E | F | Y | 49.44000 | KG | 20160913 | 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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
127358181 | 12735818 | 1 | PS | IMODIUM A-D | LOPERAMIDE HYDROCHLORIDE | 1 | Unknown | Y | N | UNKNOWN | 19860 | CAPLET | |||||||
127358181 | 12735818 | 2 | SS | IMODIUM A-D | LOPERAMIDE HYDROCHLORIDE | 1 | Unknown | Y | N | UNKNOWN | 19860 | CAPLET | |||||||
127358181 | 12735818 | 3 | SS | IMODIUM A-D | LOPERAMIDE HYDROCHLORIDE | 1 | Oral | Y | Y | 19487 | LIQUID | ||||||||
127358181 | 12735818 | 4 | SS | IMODIUM A-D | LOPERAMIDE HYDROCHLORIDE | 1 | Oral | 1/2-1 CAPFUL. | Y | Y | 19487 | LIQUID | |||||||
127358181 | 12735818 | 5 | C | FENTANYL. | FENTANYL | 1 | Unknown | 2 YEARS | 0 | 25 | MG | PATCH | QOD | ||||||
127358181 | 12735818 | 6 | C | MAGNESIUM | MAGNESIUM | 1 | Unknown | 0 | UNSPECIFIED | ||||||||||
127358181 | 12735818 | 7 | C | METOPROLOL. | METOPROLOL | 1 | Unknown | 0 | 50 | MG | UNSPECIFIED | ||||||||
127358181 | 12735818 | 8 | C | ZYRTEC | CETIRIZINE HYDROCHLORIDE | 1 | Unknown | 0 | 10 | MG | UNSPECIFIED | ||||||||
127358181 | 12735818 | 9 | C | ONDANSETRON | ONDANSETRON | 1 | Unknown | 0 | 40 | MG | UNSPECIFIED | ||||||||
127358181 | 12735818 | 10 | C | LORAZEPAM. | LORAZEPAM | 1 | Unknown | 0 | 1 | MG | UNSPECIFIED | ||||||||
127358181 | 12735818 | 11 | C | SPIRONOLACTONE. | SPIRONOLACTONE | 1 | Unknown | 0 | 50 | MG | UNSPECIFIED | ||||||||
127358181 | 12735818 | 12 | C | BUMETANIDE. | BUMETANIDE | 1 | Unknown | 0 | 1 | MG | UNSPECIFIED | ||||||||
127358181 | 12735818 | 13 | C | DIGOXIN. | DIGOXIN | 1 | Unknown | 0 | .125 | MG | UNSPECIFIED |
Indications of drugs used
Event ID | CASEID | INDI DRUG SEQ | INDI PT |
---|---|---|---|
127358181 | 12735818 | 2 | Diarrhoea |
127358181 | 12735818 | 3 | Diarrhoea |
127358181 | 12735818 | 4 | Diarrhoea |
127358181 | 12735818 | 5 | Muscle strain |
127358181 | 12735818 | 6 | Acid base balance |
127358181 | 12735818 | 7 | Acid base balance |
127358181 | 12735818 | 8 | Multiple allergies |
127358181 | 12735818 | 9 | Nausea |
127358181 | 12735818 | 10 | Nervousness |
127358181 | 12735818 | 11 | Blood pressure abnormal |
127358181 | 12735818 | 12 | Pericardial effusion |
127358181 | 12735818 | 13 | Cardiac disorder |
Outcome of event
no results found |
Reactions reported
Event ID | CASEID | DRUG REC ACT | PT |
---|---|---|---|
127358181 | 12735818 | Drug ineffective | |
127358181 | 12735818 | Dyspepsia | Dyspepsia |
127358181 | 12735818 | Incorrect dose administered |
Reporting Sources (this data is often not reported and may therefore be missing here)
no results found |
Therapies reported
no results found |