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IMPORTANT - YOUR REPORT IS QUEUED - IT MAY TAKE UP TO 12 HOURS FOR YOUR REPORT TO SHOW ON OUR HOME PAGE (IF NOT OPTED AS PRIVATE)

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Goodbye! and best wishes in your recovery

Halifax County Middle School, 1011 Middle School Cir, South Boston, VA 24592, USA

Total all time reports:  1
Latest report: May 5, 2020 12:00 PM
School food service worker tests positive for COVID -19, Halifax County Middle School, 1011 Middle School Cir, South Boston, VA 24592, USA

School food service worker tests positive for COVID -19

May 5, 2020 12:00 PM

“A Halifax County Public Schools food service worker at Halifax County Middle School has tested positive for COVID -19.

Source: wset.com See Less
Reported By SafelyHQ.com User

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Reported By SafelyHQ.com User

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“Company name: GSK Consumer Healthcare
Brand name: Robitussin
Product recalled: Cough and cold products
Reason of the recall: Incorrect dosing cups
FDA Recall date: June 18, 2020
Recall details: GSK Consumer Healthcare is voluntarily recalling to the retail level two lots (listed below) of Ch ... See Moreildren's Robitussin® Honey Cough and Chest Congestion DM and one lot of Children's Dimetapp® Cold and Cough, due to the inclusion of incorrect dosing cups. During the review of the packaging documents for these products, GSK discovered that the dosing cups for the Children's Robitussin® Honey product are missing the 5 mL and 10 mL graduations, while the dosing cups for the Children's Dimetapp® product are missing the 10 mL graduation. The dosing cups packaged with both products only have the 20 mL graduation.

There is a potential risk of accidental overdose if caregivers dispensing the syrup do not notice the discrepancies between the graduations printed on the dosing cups and the indicated amounts to be administered (as directed in the instructions for use). Children's Robitussin Honey Cough & Chest Congestion DM contains 10 mg dextromethorphan HBr USP and guaifenesin USP 100 mg per 10 mL, and is labeled for children 4 and older, as well as adults. Children's Dimetapp Cold & Cough contains 2 mg brompheniramine maleate USP, 10 mg dextromethorphan HBr USP, and 5 mg phenylephrine HCl USP per 10 mL, and is labeled for children 6 and older, as well as adults.

Symptoms of overdose of either product may include any of the following: 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.

As of the date of the recall announcement, GSK Consumer Healthcare has not received any adverse events related to these products or consumer complaints regarding the incorrect dosing cups supplied with the product. The recall is limited to the three lots listed below:

Children's Robitussin® Honey Cough and Chest Congestion DM (4oz)
NDC 0031-8760-12
Lots: 02177 (Exp. Jan. 2022) / 02178 (Exp. Jan. 2022)

Children's Dimetapp® Cold and Cough (8oz)
NDC 0031-2234-19
Lot: CL8292 (Exp. Sep. 2021)

These lots were distributed nationwide between February 5, 2020 and June 3, 2020 within the United States. GSK Consumer Healthcare has notified wholesalers, distributors and retailers to arrange for return of any recalled product. Wholesalers, distributors and retailers with an existing inventory of the lots being recalled should stop distribution and quarantine these lots immediately.

Wholesalers, distributors and retailers that have further distributed the recalled product should notify any accounts or additional locations which may have received the recalled product from them. Consumers should contact their physician or healthcare provider if they have experienced any problems that may be related to taking or using this product. Adverse reactions or quality problems experienced with the use of this product may be reported to the FDA's MedWatch Adverse Event Reporting program either online, by regular mail or by fax.

This recall is being conducted with the knowledge of the U.S. Food and Drug Administration. In December 2018, GlaxoSmithKline plc reached an agreement with Pfizer, Inc. to combine their consumer health businesses into a new Joint Venture. August 01, 2019 was the first day of the new GSK Consumer Healthcare Joint Venture. Thus, when identifying impacted product, please be aware the Pfizer company name will still be present on the label.

Check the full recall details on fda.gov

Source: FDA
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Reported By SafelyHQ.com User

March 21, 2020 3:19 PM

“Interview - Doctor in Paris, France:
This is a first-hand account from a SafelyHQ user that is a medical professional on the coronavirus situation in France. She discusses how her work has changed since the start of the pandemic, work rotations and testing for medical professionals, and issues faci ... See Moreng patients and medical professionals.

Charlotte:
I'm a pediatric resident and I work in a pediatric hospital. I was working in the genetics unit and it's mostly outpatient and non-intensive care, so we were actually closed down last week. Just because most of us are pediatricians and so we were kind of needed elsewhere. So I decided to stop working because of my pregnancy. But then all my other colleagues are still working and they're actually now, at home, confined at home and they're waiting to be called to different departments are probably either the ER or intensive care unit and from what they understand for now, they just have to stay home and rest. And they're going to be called out probably next week when the first wave of doctors start being a little tired, probably hospitalized because they themselves are sick. So right now they're mostly, resting at home. And then I know that our unit, so was shut down and a lot of other non-urgent care at our hospital was shut down and everything is being reorganized so that we have Covid units. And so at the hospital I work in, is actually a pediatric hospital, but they're going to open an adult Covid unit just because obviously adults are more affected than children are.

SafelyHQ:
Are there any changes as a pediatrician?

Charlotte:
In most maternity at least in Paris, the dads aren't allowed in the delivery room or in the hospital at all for now. So things are pretty rough on new moms right now. And I know that we're also kind of being slowly prepared that we're probably not going to be able to have an epidural just because there won't be any doctors available. So, getting prepared for maybe a rough delivery for most new moms right now, at least new Parisian moms.

SafelyHQ:
Is testing easy for people to get so far or has it been a problem for some people. And how do things look like on that front?

Charlotte:
So, in our hospital it's very easy for all medical, staff if they have any of the symptoms to get tested. It's very, very easy. I know that for patients we only test patients that are unstable or in very critical care. Just because we can't afford to test everyone, but staff is definitely prioritized and we're all told we can get tested as easily if we want to. Or if I mean, not if you want to obviously if you have symptoms.

SafelyHQ:
Did you know anyone who has got diagnosed with coronavirus?

Charlotte:
Yeah, actually, I already have a couple of friends who are staying at home because they have it. One of my, well actually he is also a pediatric resident is at home right now with, well he's getting tested today, but it's most likely Covid. His wife was tested and got tested positive after having a five day fever. And now he has a fever since yesterday, so he did his test today. So very, very likely, also Covid positive. And so his wife is also a medical resident who probably got it working at the ER and then he got it through her.

SafelyHQ:
Being in the medical field and seeing what, the medical field is doing in France and learning about, about coronavirus. And having some friends who have it, do you have any, messages that you, they have for people who want to learn more?

Charlotte:
I think just the best thing is to stay informed on what's happening on reliable sites because I know there's a lot of misinformation out there and just do what they can to stay home. Because the big wave is going to come. And I know all my friends in the hospitals are getting as ready as they can, but I'm sure you've heard that there already some parts of France that are in a very, very complicated situation where they're already out of machines for like life support machines and out of room in intensive care units. And so hopefully Paris doesn't get there, but we never know. And it all kind of just relies on people really being careful and staying home and I know everyone wants to go outside to buy their bread and whatever, but it's always a risk. And just be mindful that, yeah, doctors are doing the best they can. And I know I have friends that are pharmacist and other things like that that are complaining because they don't have masks or they're not protected. But the truth is doctors rarely have mask as well, and everyone's of kind of going through it as they can and doing the best they can. So yeah, that's the message. I think just relax, stay at home and know that everyone is trying to get organized and do the best they can, and it's obviously not perfect, but it is what it is for now.
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Reported By SafelyHQ.com User

June 5, 2020 5:00 PM

“Company name: Marksans Pharma Limited, India
Brand name: Time-Cap Labs, Inc.
Product recalled: Metformin Hydrochloride Extended-Release Tablets, USP 500mg
Reason of the recall: Due to detection of N-Nitrosodimethylamine (NDMA)
FDA Recall date: June 05, 2020
Recall details: Marksans Pharma Limi ... See Moreted, India is voluntarily recalling Metformin Hydrochloride Extended-Release Tablets, USP 500mg, lot # XP9004, to the consumer level. FDA analysis has found the product to contain N-Nitrosodimethylamine (NDMA) levels in excess of the Acceptable Daily Intake Limit (ADI) of 96ng/day. Risk Statement: NDMA is classified as a probable human carcinogen (a substance that could cause cancer) based on results from laboratory tests. NDMA is a known environmental contaminant found in water and foods, including meats, dairy products and vegetables.

Marksans Pharma Limited has not received any reports of adverse events related to this recall to date. Metformin Hydrochloride Extended-Release Tablets, USP 500mg is indicated as an adjunct to diet and exercise to improve blood glucose control in adults with type 2 diabetes mellitus and is packaged in 100 count bottles with NDC code 49483-623-01. The affected Metformin Hydrochloride Extended-Release Tablets, USP 500mg, are white to off white, capsule shaped, biconvex tablets, debossed with ‘101’ on one side and plain on the other side.

Product name: Metformin Hydrochloride Extended Release Tablets USP, 500 mg
Lot #: XP9004
Expiry Date (MM/YYYY): 12/2020

The product can be identified by lot # XP9004 and expiration date 12/2020. Metformin Hydrochloride Extended-Release Tablets, USP 500mg, lot # XP9004 was distributed by Time-Cap Labs, Inc. nationwide in the USA to wholesalers who further distributed to pharmacies. Marksans Pharma Limited is notifying its distributors and customers by issuing notification letter and press release and is arranging for return/replacement etc. of recalled product lot.

Distributors/retailers that have Metformin Hydrochloride Extended-Release Tablets, USP 500mg, lot # XP9004 which is being recalled should return to place of purchase. Consumers should contact their physician or healthcare provider if they have experienced any problems that may be related to taking or using this drug product. Adverse reactions or quality problems experienced with the use of this product may be reported to the FDA's MedWatch Adverse Event Reporting program either online, by regular mail or by fax. Complete and submit the report Online

This recall is being conducted with the knowledge of the U.S. Food and Drug Administration.
Check the full recall details on fda.gov

Source: FDA
See Less
Reported By SafelyHQ.com User