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EISAI ANNOUNCES LAUNCH OF ANTICANCER AGENT HALAVEN® AS COMPANY'S FIRST PRODUCT IN BRAZIL | News Release:2014 | Eisai Co., Ltd.
... among patients treated with Halaven were asthenia (fatigue), neutropenia, alopecia (hair loss), peripheral neuropathy (numbness ...
FDA grants accelerated approval for GSK's JEMPERLI (dostarlimab-gxly) for women with recurrent or advanced dMMR endometrial...
... were fatigue/asthenia (48%), nausea (30%), diarrhoea (26%), anaemia (24%) and constipation (20%). The most common Grade 3 or 4 ...
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FDA GRANTS FULL APPROVAL FOR BLINCYTO® (BLINATUMOMAB) TO TREAT M
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Management of COVID-19 in a Psychiatric Long-Term Care Rehabilitation Facility
Phase 3 Head-to-Head Trial Showed KYPROLIS® (Carfilzomib) Significantly Improved Overall Survival Compared To Velcade® ...
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FDA Approves LYNPARZA® (olaparib) Plus Abiraterone and Prednisone or Prednisolone for Treatment of Adult Patients With BRCA...
Study 19: nausea (71%), fatigue (including asthenia) (63%), vomiting (35%), diarrhea (28%), anemia (23%), respiratory tract ... including asthenia) (53%), anemia (41%), lymphopenia (24%), vomiting (22%), and leukopenia (18%). In addition, the most common ... including asthenia) (66%), anemia (44%), vomiting (37%), nasopharyngitis/upper respiratory tract infection (URI)/influenza (36 ... including asthenia) (38%), nausea (30%), diarrhea (19%), decreased appetite (16%), lymphopenia (14%), dizziness (14%), and ...
Takeda's QDENGA®▼ (Dengue Tetravalent Vaccine [Live, Attenuated]) Approved in Indonesia for Use Regardless of Prior Dengue...
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Immunogenicity and Safety of Tetravalent Dengue Vaccine (TDV) at the End of Shelf Life in Healthy Adults - Full Text View -...
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Renal Diseases in Cats - WSAVA2002 - VIN
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Corvelva Association - What are the vaccines against Pneumococcus?
Prelicensure clinical safety trials of Prevenar 13 (PCV13) compared this next-generation vaccine with the original Prevnar vaccine (PCV7), a vaccine inadequately studied for safety, and concerns regarding a link were reported in 2012 between febrile seizures and PCV13. It should be remembered that the pre-licensed clinical trials of the PCV7 vaccine compared its safety with that of an experimental meningitis C vaccine, seriously compromising the scientific validity of the trial. In fact, PCV13 was approved against PCV7 which was approved against an experimental meningitis C vaccine.. In clinical trials prior to the approval of PCV7, children in the groups receiving the pneumococcal vaccine suffered more from seizures, irritability, high fever and other reactions. There were 7 deaths in the PCV12 group, including 5 deaths from sudden infant death syndrome (SIDS). Long-term studies have not been completed to evaluate whether the PCV7 vaccine, given alone or in combination with other vaccines, has ...