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Maharashtra Revokes Licence Of McDonald's Outlet After Action Over Cheese
The Maharashtra Food and Drug Administration (FDA) has revoked the licence of a McDonald's outlet in the state's Ahmednagar district after taking action against it over cheese, an official said on Saturday.
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US Woman Enters MRI Machine With Loaded Gun, Gets Shot In Buttock Area
In an unusual incident, a woman in the United States was shot in her backside after she took a loaded gun into an MRI (magnetic resonance imagining) machine during a doctor's visit back in June.
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US Approves Lab-Grown Chicken To Be Sold In Markets, Twitter Reacts
The United States Department of Agriculture (USDA) has granted approvals to two companies selling chicken grown from animal cells.
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Starbucks Vanilla Frappuccino Bottles In US Recalled Over Health Safety Concerns
The US Food and Drug Administration said that more than 25,000 cases of the glass bottles have been recalled.
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US Senators Fear Facebook, Instagram Parent Meta Censoring Abortion Posts
US senators seek answers from Facebook, Instagram parent Meta regarding censored information on abortion posts. The senators questioned how many posts about abortion have been removed since the US Supreme Court overturned a long-standing right to such medical care. Meta, referring to a tweet by spokesman Andy Stone, stated that attempts to provide ...
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Elon Musk Claims His Neuralink Brain Chip Could ‘Cure’ Tinnitus in 5 Years. but Don’t Hold Your Breath
Neuralink, a Silicon Valley start-up backed by Elon Musk, has developed a neuroprosthetic brain-computer interface device. According to Musk's claims, this chip might prove useful in curing tinnitus, the neurological condition that causes ringing in your ears, within next five years. Neuroscientists back Musk's claims as they are broadly optimis...
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What To Know About COVID-19 Vaccine For US Children
The US Food and Drug Administration is considering authorizing a COVID-19 vaccine for children aged 5 to 11. The vaccine from Pfizer Inc and BioNTech SE has been available in the United States to kids aged 12 to 15 since May.
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Lupin Receives Tentative Nod For Anti-Seizure Drug; Stock Edges Higher
"The company (Lupin) has received tentative approval from the United States Food and Drug Administration (USFDA) for its abbreviated new drug application (ANDA) for Brivaracetam Tablets," Lupin said
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Lupin Gains On Receiving US FDA Nod To Launch Drug For Onychomycosis
Lupin received approval to launch Tavaborole Topical Solution, 5 per cent in United States (US) from the United States Food and Drug Administration (FDA).
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50 Lakh People Could Be Infected In Third Wave Of Covid In Maharashtra: Minister
As many as 50 lakh people including five lakh children could be infected in Maharashtra in a possible third wave of the COVID-19 pandemic, state Food and Drug Administration Minister Rajendra Shingne said on Friday.
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No Clue How BJP Got Involved In Remdesivir Issue In Maharashtra: Sources
Sources in the Food and Drugs Administration (FDA) have "no idea" how Maharashtra BJP leaders Devendra Fadnavis and Pravin Darekar became involved in the effort to procure Remdesivir for the state
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Maharashtra To Face Shortage Of Remidesivir For Next 2 To 3 Days: Minister
Maharashtra will face a shortage of 12,000 to 15,000 Remdesivir injections, used to treat COVID-19 patients, for the next two to three days, state Food and Drug Administration (FDA) Minister Rajendra Shingane said on Friday.
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US Drug Regulator Investigating 5 Allergic Reactions After Pfizer Shot
The US Food and Drug Administration is investigating around five allergic reactions that happened after people were administered Pfizer Inc and BioNTech SE's COVID-19 vaccine in the United States this week, a top FDA official said late on Friday.
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US Authorises First Rapid At-Home Covid-19 Test
The United States on Tuesday authorized its first rapid at-home test for Covid-19, which is available over-the-counter and produces a result in around 20 minutes.
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Glenmark Pharma Gets Regulatory Nod For Tacrolimus Capsules; Stock Gains Nearly 2%
Glenmark Pharma received final approval from USFDA for Tacrolimus capsules, which are used as immunosuppressants to prevent human immune system from rejecting liver, kidney and heart transplants.
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Maharashtra Revokes Licence Of McDonald's Outlet After Action Over Cheese
The Maharashtra Food and Drug Administration (FDA) has revoked the licence of a McDonald's outlet in the state's Ahmednagar district after taking action against it over cheese, an official said on Saturday.
-
US Woman Enters MRI Machine With Loaded Gun, Gets Shot In Buttock Area
In an unusual incident, a woman in the United States was shot in her backside after she took a loaded gun into an MRI (magnetic resonance imagining) machine during a doctor's visit back in June.
-
US Approves Lab-Grown Chicken To Be Sold In Markets, Twitter Reacts
The United States Department of Agriculture (USDA) has granted approvals to two companies selling chicken grown from animal cells.
-
Starbucks Vanilla Frappuccino Bottles In US Recalled Over Health Safety Concerns
The US Food and Drug Administration said that more than 25,000 cases of the glass bottles have been recalled.
-
US Senators Fear Facebook, Instagram Parent Meta Censoring Abortion Posts
US senators seek answers from Facebook, Instagram parent Meta regarding censored information on abortion posts. The senators questioned how many posts about abortion have been removed since the US Supreme Court overturned a long-standing right to such medical care. Meta, referring to a tweet by spokesman Andy Stone, stated that attempts to provide ...
-
Elon Musk Claims His Neuralink Brain Chip Could ‘Cure’ Tinnitus in 5 Years. but Don’t Hold Your Breath
Neuralink, a Silicon Valley start-up backed by Elon Musk, has developed a neuroprosthetic brain-computer interface device. According to Musk's claims, this chip might prove useful in curing tinnitus, the neurological condition that causes ringing in your ears, within next five years. Neuroscientists back Musk's claims as they are broadly optimis...
-
What To Know About COVID-19 Vaccine For US Children
The US Food and Drug Administration is considering authorizing a COVID-19 vaccine for children aged 5 to 11. The vaccine from Pfizer Inc and BioNTech SE has been available in the United States to kids aged 12 to 15 since May.
-
Lupin Receives Tentative Nod For Anti-Seizure Drug; Stock Edges Higher
"The company (Lupin) has received tentative approval from the United States Food and Drug Administration (USFDA) for its abbreviated new drug application (ANDA) for Brivaracetam Tablets," Lupin said
-
Lupin Gains On Receiving US FDA Nod To Launch Drug For Onychomycosis
Lupin received approval to launch Tavaborole Topical Solution, 5 per cent in United States (US) from the United States Food and Drug Administration (FDA).
-
50 Lakh People Could Be Infected In Third Wave Of Covid In Maharashtra: Minister
As many as 50 lakh people including five lakh children could be infected in Maharashtra in a possible third wave of the COVID-19 pandemic, state Food and Drug Administration Minister Rajendra Shingne said on Friday.
-
No Clue How BJP Got Involved In Remdesivir Issue In Maharashtra: Sources
Sources in the Food and Drugs Administration (FDA) have "no idea" how Maharashtra BJP leaders Devendra Fadnavis and Pravin Darekar became involved in the effort to procure Remdesivir for the state
-
Maharashtra To Face Shortage Of Remidesivir For Next 2 To 3 Days: Minister
Maharashtra will face a shortage of 12,000 to 15,000 Remdesivir injections, used to treat COVID-19 patients, for the next two to three days, state Food and Drug Administration (FDA) Minister Rajendra Shingane said on Friday.
-
US Drug Regulator Investigating 5 Allergic Reactions After Pfizer Shot
The US Food and Drug Administration is investigating around five allergic reactions that happened after people were administered Pfizer Inc and BioNTech SE's COVID-19 vaccine in the United States this week, a top FDA official said late on Friday.
-
US Authorises First Rapid At-Home Covid-19 Test
The United States on Tuesday authorized its first rapid at-home test for Covid-19, which is available over-the-counter and produces a result in around 20 minutes.
-
Glenmark Pharma Gets Regulatory Nod For Tacrolimus Capsules; Stock Gains Nearly 2%
Glenmark Pharma received final approval from USFDA for Tacrolimus capsules, which are used as immunosuppressants to prevent human immune system from rejecting liver, kidney and heart transplants.
