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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
127716891 | 12771689 | 1 | I | 20160913 | 20160922 | 20160922 | EXP | SA-PERRIGO-16SA019981 | PERRIGO | 42.00 | YR | M | Y | 0.00000 | 20160922 | PH | SA | SA |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
127716891 | 12771689 | 1 | PS | ACETAMINOPHEN. | ACETAMINOPHEN | 1 | Unknown | 4 G, QD | U | U | UNKNOWN | 75077 | 4 | G | MODIFIED-RELEASE TABLET | QD | |||
127716891 | 12771689 | 2 | SS | LORMETAZEPAM | LORMETAZEPAM | 1 | Unknown | UNK | U | UNKNOWN | 0 |
Indications of drugs used
Event ID | CASEID | INDI DRUG SEQ | INDI PT |
---|---|---|---|
127716891 | 12771689 | 1 | Back pain |
127716891 | 12771689 | 2 | Back pain |
Outcome of event
Event ID | CASEID | OUTC COD |
---|---|---|
127716891 | 12771689 | HO |
Reactions reported
Event ID | CASEID | DRUG REC ACT | PT |
---|---|---|---|
127716891 | 12771689 | Abdominal pain | |
127716891 | 12771689 | Hepatic encephalopathy | |
127716891 | 12771689 | Nausea | |
127716891 | 12771689 | Poisoning | |
127716891 | 12771689 | Renal impairment | |
127716891 | 12771689 | Vomiting |
Reporting Sources (this data is often not reported and may therefore be missing here)
no results found |
Therapies reported
no results found |