中山肛门长火疙瘩(中山市有治疗痔疮的机构吗) (今日更新中)

Update, 5:05 p.m. ET: It appears an outage to the IRS' e-file system has been fixed. For much of Tuesday, the IRS website had a glitch, preventing some from completing their taxes. Tuesday was the last day to file 2017 taxes.Previous story:The IRS gave people another reason to get their taxes done early. The IRS online payment option to pay with a bank account went down Tuesday with hours to go before the Tax Day deadline. As of 12:20 p.m. Eastern, the site had an alert telling customers "This service is currently unavailable. We apologize for any inconvenience." Late filers could still pay by credit or debit card, but those payments come with fees.   702

Tuesday marks the final day for Americans to sign up for health insurance through the Affordable Care Act.Tuesday marks the last day for open enrollment for the public health insurance commonly referred to as "Obamacare."The COVID-19 pandemic has left millions without a job and more vulnerable to health issues than ever. While many Americans will be without employer-provided healthcare, people in most states are still able to pick a public plan through the Affordable Care Act.According to the Centers for Medicare & Medicaid Services, 3.8 million Americans have selected a health care plan provided through the Affordable Care Act during the current enrollment period. Between Nov. 29 and Dec. 5 alone, more than 900,000 Americans selected a public health care plan.To sign up for a plan through to the Affordable Care Act, visit HealthCare.gov and click "take the first steps to apply." From there, customers will enter some initial information and will then be able to pick a plan from the ACA Health Insurance Marketplace or be directed to a health insurance marketplace website run by your state.Customers can also sign up for an ACA health insurance plan by calling 1-800-318-2596. 1200

Two children’s cough syrups are being recalled because of a defect that could cause overdosing.GlaxoSmithKline Consumer Healthcare is voluntarily recalling two lots of Children's Robitussin? Honey Cough and Chest Congestion DM and one lot of Children's Dimetapp? Cold and Cough. (see below for details) The products were sold between February 5 and June 3 of this year.According to the FDA, during a review of the packaging, the drug company discovered the dosing cups were missing the 5mL and 10mL graduations. Without the measurement labels, there is a concern parents will not give their child recommended dosing.Symptoms of overdose of the ingredients in these cough syrup products include: impaired coordination; brain stimulation causing increase in energy, elevation in blood pressure, heart rate, and respiration; a lack of energy and enthusiasm; severe dizziness or drowsiness; slow heart rate; fainting; psychotic behaviour; restlessness; seizure; decreased respiration; nausea; vomiting; constipation; diarrhea; abdominal pain; visual and hearing hallucinations; urinary retention.GSK Consumer Healthcare has not received any reports of overdosing or issues at this time.The recall is limited to the following items:Children's Robitussin? Honey Cough and Chest Congestion DM (4oz)NDC 0031-8760-12Lots: 02177 (Exp. Jan. 2022)02178 (Exp. Jan. 2022)Children's Dimetapp? Cold and Cough (8oz)NDC 0031-2234-19Lot: CL8292 (Exp. Sep. 2021) 1450

Two people had to be rescued by West Palm Beach, Fla. firefighters after a dog attack Monday morning. West Palm Beach Fire Rescue said the incident occurred in the north end of the city.Fire officials said a man and a woman were in their second-story apartment when they were bitten by their own dog.Firefighters had to use a ladder to get the couple out of their apartment.No other details were immediately available. 441

U.S. officials say the nation’s first COVID-19 vaccine will begin arriving in states Monday morning. Army Gen. Gustave Perna said Saturday that trucks will roll out Sunday morning as shipping companies UPS and FedEx begin delivering Pfizer’s vaccine to nearly 150 distribution centers across the states. An additional 425 sites will get shipments Tuesday, and the remaining 66 on Wednesday. Perna is with Operation Warp Speed, the Trump administration’s vaccine development program. Initially, about 3 million doses are expected to be shipped nationwide, with priority going to health care workers and nursing home residents.The FDA called the vaccine from Pfizer and its German partner BioNTech safe and strongly protective.After the FDA approved the vaccine, President Donald Trump thanked the FDA and praised both Pfizer and Moderna in a video posted to his Twitter account.But initial doses are scarce and rationed, with health workers and nursing home residents first in line.According to the Associated Press, about 3 million doses of the vaccine are expected in the first shipments around the country, according to officials with Operation Warp Speed.In a letter of authorization, the FDA said that in an ongoing trial of 44,000 people, the agency found the vaccine was safe and more than 90% effective in older adults.In a press release, the FDA said participants in the trial complained of several side effects, which included pain at the injection site, tiredness, headache, muscle pain, chills, joint pain, and fever.The FDA added that these side effects typically lasted several days, and people experienced the side effects after the second dose than after the first dose.“While not an FDA approval, today’s emergency use authorization of the Pfizer-BioNTech COVID-19 Vaccine holds the promise to alter the course of this pandemic in the United States,” said Peter Marks, M.D., Ph.D., Director of the FDA’s Center for Biologics Evaluation and Research in the press release.Enough for the general population isn't expected until spring, and experts urge people to mask up and keep their distance during a long, grim winter.“Today’s action follows an open and transparent review process that included input from independent scientific and public health experts and a thorough evaluation by the agency’s career scientists to ensure this vaccine met FDA’s rigorous, scientific standards for safety, effectiveness, and manufacturing quality needed to support emergency use authorization," said FDA Commissioner Stephen M. Hahn, M.D. in the press release. 2570

来源：资阳报