In an enormous victory for women and girls across the nation, the Food and Drug Administration finally approved the Plan B One-Step brand morning-after pill for over-the-counter use. Plan B One-Step is a one-pill version of emergency contraception and this approval covers women and girls of all ages. Like all EC, it is more effective the sooner it is taken after unprotected sex. If taken within 72 hours of unprotected sex, EC is almost 90 percent more effective at preventing unwanted pregnancy.
Earlier this month, the Obama administration backed off its resistance to making the morning-after pill accessible OTC to women and girls of all ages. Previously, Obama had been against girls younger than 15 being able to access the pill. Keep reading »
This is why we can’t have nice things, America.
On Tuesday, the Food and Drug Administration announced the age to purchase the morning-after pill would be lowered to 15 and it would be available on shelves instead of behind-the-counter. The decision was prompted by a federal judge having struck down the “age-17 and over without a prescription” limit back in April. But no more: yesterday, the Justice Department announced its plans to appeal the federal court decision, claiming, The Washington Post reports, the federal judge “overstepped his authority.” Keep reading »
Fathers, lock up your daughters: the government is going to be forcing slutty slut pills down their throats!
That will be the Fox News version of events. But here in Reasonable, Common Sense-land, the story is different: a federal judge — a man! — has struck down the age limit on the morning-after pill, meaning sexually active young women age 16 and younger will be able to access it. Ruling on a lawsuit by the Center for Reproductive Rights, Judge Edward Korman decided that the government’s refusal to lift the age restriction is “arbitrary, capricious and unreasonable” and said the FDA’s feet-dragging has been an “obstruction.” He ordered the FDA to lift the age restriction within 30 days.
Reproductive rights activists pushed the FDA for years to make Plan B accessible to all and in 2011, they finally did. But it never happened: Health and Human Services Secretary swiftly overruled the FDA recommendation to make Plan B accessible to everyone, citing alleged concern about its safety for young teens — but in reality, kowtowing to a game of keep-conservatives-happy hardball. Keep reading »
Conservatives losing their marbles to start in five … four … three … two … one: the FDA has until tomorrow to decide whether the morning-after pill Plan B will be available on drugstore shelves (as opposed to behind the counter) without a prescription for anyone of any age. If taken within 72 hours of unprotected sex, Plan B is almost 90 percent effective in preventing a pregnancy. The sooner Plan B is taken after unprotected sex, the more effective it is. Keep reading »
Good luck getting your hair straightened via Brazilian Blowout after next week — the Food and Drug Administration has come down hardcore on the hair straightening company for the high amount of formaldehyde found in its product. According to the FDA, the amount of formaldehyde found in Brazilian Blowout and similar hair straightening treatments is considered dangerous when inhaled and both salon workers and customers have complained of a variety of ailments related to the product’s use. Keep reading »
Time to stock up on the Horny Goat Weed instead, you guys! (Just kidding.) The FDA issued a warning on Wednesday for Man Up Now, a “dietary supplement for men’s sexual arousal” because it could dangerously lower blood pressure. Although Man Up Now capsules market themselves as “all natural” and “herbal,” they contain an active drug found in Viagra called sulfoaildenafil. Sulfoaildenafil can cause blood pressure to plummet through the carpet and make you dizzy and lightheaded. So stop operating heavy machinery, you randy little minxes, and ditch your Man Up Now pills immediately, per FDA request. Keep reading »
It’s like Prohibition for sloppy drunk college kids! Hot on the heels of Phusion Projects voluntarily offering to remove caffeine from its “blackout in a can” drink Four Loko yesterday morning, the FDA has also warned four alcoholic energy drink makers that they all must either stop adding caffeine or kill the products. Phusion Projects, Charge Beverages (which makes Core High Gravity drinks), New Century Brewing (which makes Moonshot) and United Brands (which makes Joose) all received warning letters threatening to seize the alcoholic energy drinks from stores and to get a judge to ban their sales. The combo of liquor and caffeine causes “a state of wide-awake drunk” which can lead to “hazardous and life-threatening situations,” the FDA warned. Understatement of the year, you think? Keep reading »
Stock up on your Four Loko now, kiddies! (Just kidding.) Following a string of deaths and near-deaths around the country related to alcoholic energy drinks, the FDA might crack down on manufacturers as soon as tomorrow. The FDA has been reviewing the safety of these “blackout in a can” drinks for a year. But it’s getting a kick in the pants to act more quickly now that the liquor authorities in several states — such as Washington, where nine college kids recently fell ill — are in various stages of banning the party drinks. Distributors are closing in as well: New York’s largest beer distributor announced yesterday that it would stop selling alcoholic energy drinks and it will clear its inventory by December 10th. Keep reading »
When you pick up a fancy “organic” powder, do you actually know what that means? We don’t. But we somehow have the impression that it’s a more wholesome and healthy product produced in a verdant field, far, far away from any industrial factories. Time to get educated. A recent report released by the FDA sets the record straight about what the organic label means.
What qualifies a beauty product as organic? Well[FDA.gov] Keep reading »