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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

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

UPDATE: San Diego Police say the girls have been safely located at a friend's house.SAN DIEGO (CNS) - Two girls, aged 10 and 12, who did not return home 160

Uber is adding another transportation option on its app: the electric bike.The new electric motor option called JUMP is just in a few cities right now, but the company hopes to soon make it nationwide.“It's part of a growing mobile effort by Uber to provide all kinds of modes of transportation,” says Dave Nelson, director of operations for JUMP Bikes. “JUMP is an electric, dockless bike that allows you to go further faster and have more fun doing it.”  Similar to electric scooters, the bikes start at ; for every minute after the first, it costs UPDATE (8:45 a.m., May 24): San Diego police say Gregory Gavino was found at a family's home at about 8 a.m. and taken back to the hospital. No other details were provided. 180.15.Users log into their Uber app in order to request the bike. The app tells you where the bike is located. Once you find your bike, you simply punch in a code and the bike is yours to use.So, what makes Jump bikes different than the motorized transportation options already available?“It is a dockless bike that allows you to pick it up, lock it, drop it off anywhere that's convenient for you,” explains Nelson. “And then, the biggest difference is, that it's electric. It takes you 20 miles per hour and lets you get to where you are going a little quicker.” 1130

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