Anti-depressant Drug
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Researchers Find That Anti-Depressants Could Raise The Risk Of Intestinal Bleeding
Patients taking anti-depressant medications classified as selective serotonin reuptake inhibitors (SSRIs) are 40 per cent more likely to develop severe gastrointestinal bleeding, according to a research review in the Journal of the American Osteopathic Association.
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Indrani Mukerjea Had Drug Overdose, Confirms Test, Says Hospital
Former media executive Indrani Mukerjea, arrested for the alleged killing of her daughter Sheena Bora, had an overdose of anti-depressant drugs not prescribed to her, Mumbai's J J Hospital said, quoting forensic lab reports.
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Here's Why You Shouldn't Take Antidepressants During Pregnancy?
Mothers who opted for anti-depressants during their pregnancy may have put their children at a risk of autism according to a new study.
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Cheers! Your Evening Drink May Work As Anti-Depressant
Can having a few drinks help people with clinical depression feel better and behave normally? Yes, at least in terms of biochemistry. Researchers have found that alcohol produces the same neural and molecular changes as drugs that have proven to be rapidly effective anti-depressants.
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Prescribing Anti-Depressants To Children Raised By 30% In 10 Years: Study
A recent study says that though there's a steep rise in prescribing of anti-depressants to children over the last decade, more than 40 percent are drugs, which do not work and can even have toxic side-effects.
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Dr Reddy's Launches Generic Anti-Depressant Drug In US
The company has launched the drug in strengths of 100 mg, 150 mg and 200 mg, Dr Reddy's Laboratories said in a regulatory filing.
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Zydus Recalls Over Two Lakh Bottles Of Anti-Depressant Drug In US
Zydus Cadila is recalling over two lakh bottles of anti-depressant Venlafaxine HCL ER capsules in the US in two different strengths for failed dissolution specifications.
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Researchers Find Why Anti-Depressants Take So Long To Work
Researchers have discovered a reason why anti-depressants can take up to two months to work, and their finding could help scientists develop faster-acting drugs in the future.
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Sun Pharma Recalls 16,000 Bottles Of Antidepressant Tablets In US
Drug major Sun Pharmaceutical Industries is recalling over 16,000 bottles of anti-depressant tablets from the US market due to failed dissolution specifications.
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UK Competition Authorities Fine GlaxoSmithKline $54.5 Million
Britain's competition authority has fined drug maker GlaxoSmithKline plc 37.6 million pounds ($54.5 million) for stalling the potential entry of generic competitors of an anti-depressant drug Seroxat into the marketplace.
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Glenmark Settles Patent Litigation Over Anti-depressant Drug
Glenmark Pharmaceuticals on Monday announced a patent litigation settlement with Forest Laboratories and Royalty Pharma Collection Trust over anti-depressant drug Savella.The company and its US arm Glenmark Pharmaceuticals Inchave entered into a settlement agreement with Forest Laboratories LLC, Forest Laboratories Holdings Ltd and Royalty Pharma C...
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Jubilant Life Zooms 10% on USFDA Nod for Anti-Depressant Drug
Jubilant Life Sciences shares soared almost 10 per cent, to touch its fresh 52-week high on Tuesday, as the company received final approval from the US health regulator for its generic version of anti-depressant Paxil tablets.
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Sun Pharma Recalls 68,194 Bottles of Anti-Depression Drug in US
As per the information available on the USFDA website, Sun Pharma Global Inc, a unit of the company, is recalling the drug for failing "dissolution specification".
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Sun Pharma Recalls Over 4 Lakh Bottles of 2 Drugs in US: Report
Drug major Sun Pharmaceuticals is recalling over 4 lakh bottles of anti-depressant and anti-allergy drugs in the US for failing to meet specifications.
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Lupin, Sun among firms to get FDA nod for anti-depressant drug
Aurobindo Pharma, Dr Reddy's Laboratories, Lupin, Sun Pharma Global FZE, and Torrent Pharmaceuticals have received the regulatory nod to market duloxetine in various strengths, besides Teva Pharmaceuticals, USA, says a press release issued by the FDA.
-
Researchers Find That Anti-Depressants Could Raise The Risk Of Intestinal Bleeding
Patients taking anti-depressant medications classified as selective serotonin reuptake inhibitors (SSRIs) are 40 per cent more likely to develop severe gastrointestinal bleeding, according to a research review in the Journal of the American Osteopathic Association.
-
Indrani Mukerjea Had Drug Overdose, Confirms Test, Says Hospital
Former media executive Indrani Mukerjea, arrested for the alleged killing of her daughter Sheena Bora, had an overdose of anti-depressant drugs not prescribed to her, Mumbai's J J Hospital said, quoting forensic lab reports.
-
Here's Why You Shouldn't Take Antidepressants During Pregnancy?
Mothers who opted for anti-depressants during their pregnancy may have put their children at a risk of autism according to a new study.
-
Cheers! Your Evening Drink May Work As Anti-Depressant
Can having a few drinks help people with clinical depression feel better and behave normally? Yes, at least in terms of biochemistry. Researchers have found that alcohol produces the same neural and molecular changes as drugs that have proven to be rapidly effective anti-depressants.
-
Prescribing Anti-Depressants To Children Raised By 30% In 10 Years: Study
A recent study says that though there's a steep rise in prescribing of anti-depressants to children over the last decade, more than 40 percent are drugs, which do not work and can even have toxic side-effects.
-
Dr Reddy's Launches Generic Anti-Depressant Drug In US
The company has launched the drug in strengths of 100 mg, 150 mg and 200 mg, Dr Reddy's Laboratories said in a regulatory filing.
-
Zydus Recalls Over Two Lakh Bottles Of Anti-Depressant Drug In US
Zydus Cadila is recalling over two lakh bottles of anti-depressant Venlafaxine HCL ER capsules in the US in two different strengths for failed dissolution specifications.
-
Researchers Find Why Anti-Depressants Take So Long To Work
Researchers have discovered a reason why anti-depressants can take up to two months to work, and their finding could help scientists develop faster-acting drugs in the future.
-
Sun Pharma Recalls 16,000 Bottles Of Antidepressant Tablets In US
Drug major Sun Pharmaceutical Industries is recalling over 16,000 bottles of anti-depressant tablets from the US market due to failed dissolution specifications.
-
UK Competition Authorities Fine GlaxoSmithKline $54.5 Million
Britain's competition authority has fined drug maker GlaxoSmithKline plc 37.6 million pounds ($54.5 million) for stalling the potential entry of generic competitors of an anti-depressant drug Seroxat into the marketplace.
-
Glenmark Settles Patent Litigation Over Anti-depressant Drug
Glenmark Pharmaceuticals on Monday announced a patent litigation settlement with Forest Laboratories and Royalty Pharma Collection Trust over anti-depressant drug Savella.The company and its US arm Glenmark Pharmaceuticals Inchave entered into a settlement agreement with Forest Laboratories LLC, Forest Laboratories Holdings Ltd and Royalty Pharma C...
-
Jubilant Life Zooms 10% on USFDA Nod for Anti-Depressant Drug
Jubilant Life Sciences shares soared almost 10 per cent, to touch its fresh 52-week high on Tuesday, as the company received final approval from the US health regulator for its generic version of anti-depressant Paxil tablets.
-
Sun Pharma Recalls 68,194 Bottles of Anti-Depression Drug in US
As per the information available on the USFDA website, Sun Pharma Global Inc, a unit of the company, is recalling the drug for failing "dissolution specification".
-
Sun Pharma Recalls Over 4 Lakh Bottles of 2 Drugs in US: Report
Drug major Sun Pharmaceuticals is recalling over 4 lakh bottles of anti-depressant and anti-allergy drugs in the US for failing to meet specifications.
-
Lupin, Sun among firms to get FDA nod for anti-depressant drug
Aurobindo Pharma, Dr Reddy's Laboratories, Lupin, Sun Pharma Global FZE, and Torrent Pharmaceuticals have received the regulatory nod to market duloxetine in various strengths, besides Teva Pharmaceuticals, USA, says a press release issued by the FDA.
