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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 125978221 | 12597822 | 1 | I | 201509 | 20151113 | 20160726 | 20160726 | PER | US-MYLANLABS-2015M1040326 | MYLAN | 69.00 | YR | M | Y | 103.40000 | KG | 20160726 | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 125978221 | 12597822 | 1 | PS | Atorvastatin Calcium Tablets | ATORVASTATIN CALCIUM | 1 | Oral | 40 MG, QD | 3037171 | 91226 | 40 | MG | TABLET | QD | |||||
| 125978221 | 12597822 | 2 | C | DEXILANT | DEXLANSOPRAZOLE | 1 | Oral | 60 MG, QD | 0 | 60 | MG | QD | |||||||
| 125978221 | 12597822 | 3 | C | NAPROXEN. | NAPROXEN | 1 | Oral | UNK, PRN | 0 | ||||||||||
| 125978221 | 12597822 | 4 | C | LORATADINE. | LORATADINE | 1 | Oral | UNK, QD, PRN | 0 | QD | |||||||||
| 125978221 | 12597822 | 5 | C | DOCUSATE SODIUM. | DOCUSATE SODIUM | 1 | Oral | 100 MG, QD | 0 | 100 | MG | QD | |||||||
| 125978221 | 12597822 | 6 | C | MULTIVITAMIN /00097801/ | VITAMINS | 1 | UNK | 0 | |||||||||||
| 125978221 | 12597822 | 7 | C | OMEGA 3 /01334101/ | OMEGA-3 FATTY ACIDS | 1 | UNK | 0 | |||||||||||
| 125978221 | 12597822 | 8 | C | PROBIOTICS /07325001/ | BIFIDOBACTERIUM LONGUMLACTOBACILLUS ACIDOPHILUSLACTOBACILLUS RHAMNOSUS | 1 | UNK | U | 0 |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 125978221 | 12597822 | 1 | Blood cholesterol increased |
Outcome of event
| no results found |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 125978221 | 12597822 | Dysgeusia |
Reporting Sources (this data is often not reported and may therefore be missing here)
| no results found |
Therapies reported
| no results found |