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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 118959466 | 11895946 | 6 | F | 20160712 | 20160107 | 20160714 | EXP | FR-PFIZER INC-2015478539 | PFIZER | 4.00 | YR | M | Y | 16.00000 | KG | 20160714 | OT | FR | FR |
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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 118959466 | 11895946 | 1 | PS | ZITHROMAX | AZITHROMYCIN DIHYDRATE | 1 | UNK | 50710 | POWDER FOR ORAL SUSPENSION | ||||||||||
| 118959466 | 11895946 | 2 | I | COLCHICINE OPOCALCIUM | COLCHICINE | 1 | 8 MG OF COLCHICINE 2 TIMES A DAY (16 TABLETS OF 0.5 MG CRUSHED WITH A BIT OF WATER). | 0 | 8 | MG | |||||||||
| 118959466 | 11895946 | 3 | C | PARACETAMOL | ACETAMINOPHEN | 1 | UNK | 0 |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 118959466 | 11895946 | 2 | Pericarditis |
Outcome of event
| Event ID | CASEID | OUTC COD |
|---|---|---|
| 118959466 | 11895946 | OT |
| 118959466 | 11895946 | DE |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 118959466 | 11895946 | Diarrhoea | |
| 118959466 | 11895946 | Drug interaction | |
| 118959466 | 11895946 | Toxicity to various agents | |
| 118959466 | 11895946 | Vomiting |
Reporting Sources (this data is often not reported and may therefore be missing here)
| no results found |
Therapies reported
| no results found |