| Name | Number of Reports | Reference(s) | Data Source | |
|---|---|---|---|---|
| 1 | Headache | FAERS: 17 | US FAERS | |
| 2 | Nausea | FAERS: 13 | US FAERS | |
| 3 | Fatigue | FAERS: 9 | US FAERS | |
| 4 | Asthenia | FAERS: 5 | US FAERS | |
| 5 | Abdominal Pain | FAERS: 4 | US FAERS | |
| 6 | Inappropriate schedule of product administration | FAERS: 4 | US FAERS | |
| 7 | Product use complaint | FAERS: 4 | US FAERS | |
| 8 | Vomiting | FAERS: 4 | US FAERS | |
| 9 | Dizziness | FAERS: 3 | US FAERS | |
| 10 | Drug ineffective | FAERS: 3 | US FAERS | |
| 11 | Portal Vein Thrombosis | FAERS: 3 | US FAERS | |
| 12 | Abdominal discomfort | FAERS: 2 | US FAERS | |
| 13 | Disorientation | FAERS: 2 | US FAERS | |
| 14 | Feeling abnormal | FAERS: 2 | US FAERS | |
| 15 | Hepatic Encephalopathy | FAERS: 2 | US FAERS | |
| 16 | Myocardial Infarction | FAERS: 2 | US FAERS | |
| 17 | Peripheral swelling | FAERS: 2 | US FAERS | |
| 18 | Somnolence | FAERS: 2 | US FAERS | |
| 19 | Accidental underdose | FAERS: 1 | US FAERS | |
| 20 | Acute myocardial infarction | FAERS: 1 | US FAERS | |
| 21 | Ammonia increased | FAERS: 1 | US FAERS | |
| 22 | Back Pain | FAERS: 1 | US FAERS | |
| 23 | Cold sweat | FAERS: 1 | US FAERS | |
| 24 | Constipation | FAERS: 1 | US FAERS | |
| 25 | Cystitis | FAERS: 1 | US FAERS | |
| 26 | Depressed mood | FAERS: 1 | US FAERS | |
| 27 | Drug effect incomplete | FAERS: 1 | US FAERS | |
| 28 | Epistaxis | FAERS: 1 | US FAERS | |
| 29 | Incorrect dose administered | FAERS: 1 | US FAERS | |
| 30 | Initial insomnia | FAERS: 1 | US FAERS | |
| 31 | Joint swelling | FAERS: 1 | US FAERS | |
| 32 | Malaise | FAERS: 1 | US FAERS | |
| 33 | Musculoskeletal discomfort | FAERS: 1 | US FAERS | |
| 34 | No adverse event | FAERS: 1 | US FAERS | |
| 35 | Pain | FAERS: 1 | US FAERS | |
| 36 | Platelet aggregation abnormal | FAERS: 1 | US FAERS | |
| 37 | Platelet count abnormal | FAERS: 1 | US FAERS | |
| 38 | Pneumonia | FAERS: 1 | US FAERS | |
| 39 | Product administration error | FAERS: 1 | US FAERS | |
| 40 | Product dose omission | FAERS: 1 | US FAERS | |
| 41 | Product label confusion | FAERS: 1 | US FAERS | |
| 42 | Product packaging confusion | FAERS: 1 | US FAERS | |
| 43 | Product prescribing error | FAERS: 1 | US FAERS | |
| 44 | Product prescribing issue | FAERS: 1 | US FAERS | |
| 45 | Product use in unapproved indication | FAERS: 1 | US FAERS | |
| 46 | Product use issue | FAERS: 1 | US FAERS | |
| 47 | Pruritus | FAERS: 1 | US FAERS | |
| 48 | Pulmonary Embolism | FAERS: 1 | US FAERS | |
| 49 | Sweating fever | FAERS: 1 | US FAERS | |
| 50 | Swelling | FAERS: 1 | US FAERS | |
| 51 | Syncope | FAERS: 1 | US FAERS | |
| 52 | Thrombosis | FAERS: 1 | US FAERS | |
| 53 | White blood cell count decreased | FAERS: 1 | US FAERS |
Page last updated at 2020-05-25 10:01:57 (Asia/Shanghai) | You are visitor No. 120237
Copyright © 2019-2020 Laboratory of Molecular Modeling and Design, Shanghai Key Laboratory of New Drug Design, School of Pharmacy, East China University of Science and Technology. All rights reserved.