रूस की वैक्सीन का भारत में होगा ट्रायल, DCGI ने दी अनुमति

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  • License of fake medicine manufacturers cancelled | DCGI | CDSCO #shorts

    License of fake medicine manufacturers cancelled | DCGI | CDSCO #shorts

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    License of fake medicine manufacturers cancelled | DCGI | CDSCO #shorts

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    License of fake medicine manufacturers cancelled | DCGI | CDSCO #shorts

    oleh Bharatiya Janata Party Delhi| 48 dilihat

  • DCGI | Digene Gel | Stop Consumption |

    DCGI | Digene Gel | Stop Consumption |

    If you also consume Digene Gel due to stomach upset, then stop doing so immediately. Now the Drugs Controller General of India has issued an advisory alert regarding the company's antacid syrup, Digene Gel. Along with this, patients have been advised to immediately stop the consumption of Digene gel prepared at the Goa plant.
    ............................
    #DigeneGel #stomachupset #DrugControllerGeneralofIndia #antacidsyrup #patients #Goaplant #himachalabhiabhi #analpatrwal
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    DCGI | Digene Gel | Stop Consumption |

    oleh Himachal Abhi Abhi| 35 dilihat

  • DCGI / DRUG_ALERT / drug alert / Chlorpheniramine_Maleate

    DCGI / DRUG_ALERT / drug alert / Chlorpheniramine_Maleate

    The Drugs Controller General of India has issued a drug alert regarding cough syrup containing fixed combination of chlorpheniramine maleate and phenylephrine. Syrups containing these combinations are commonly used to treat cold, cough and flu. The Drugs Controller General of India issued a letter related to this to the states and union territories on December 18. It clearly states that FDC should not be used for children below 4 years.
    ...........................
    #Drugs_Controller_General_of_India #Drug_Alert #Chlorpheniramine_Maleate #Phenylephrine #FDC #Himachalabhiabhi
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    DCGI / DRUG_ALERT / drug alert / Chlorpheniramine_Maleate

    oleh Himachal Abhi Abhi| 16 dilihat

  • DCGI accepts expert committee report to allow Covaxin jabs without clinical trial

    DCGI accepts expert committee report to allow Covaxin jabs without clinical trial

    DCGI accepts recommendations of Subject Expert Committee (SEC) to no longer administer Covaxin in 'clinical trial mode'. The SEC of Drugs Controller General of India (DCGI) on Wednesday recommended removing the "clinical trial mode" condition related to Bharat Biotech's Covaxin. This entails that the beneficiaries will not be required to sign a consent form to take the indigenous COVID-19 vaccine if the SEC recommendation is accepted by the country's top drugs regulator.

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    DCGI accepts expert committee report to allow Covaxin jabs without clinical trial

    oleh The Economic Times| 207 dilihat

  • Covid-19: DCGI extends shelf life of Covishield to 9 months from manufacturing date

    Covid-19: DCGI extends shelf life of Covishield to 9 months from manufacturing date

    India's drug regulator DCGI has extended the shelf life of Covishield, the Oxford-AstraZeneca COVID-19 vaccine, from six to nine months from its manufacturing date. In a letter to the Serum Institute of India, Drugs Controller General of India V G Somani said the SII is permitted to apply the shelf life of nine months to unlabelled vials available on hand.

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    Covid-19: DCGI extends shelf life of Covishield to 9 months from manufacturing date

    oleh The Economic Times| 176 dilihat

  • Zydus Cadila की विराफिन दवा करेगी कोरोना दूर? DCGI ने इस्तेमाल के लिए दी मंजूरी

    Zydus Cadila की विराफिन दवा करेगी कोरोना दूर? DCGI ने इस्तेमाल के लिए दी मंजूरी

    देश में कोरोना महामारी ने कोहराम मचा रखा है... देश में दवा से लेकर ऑक्सीजन तक की किल्लत हो रही है... इसी बीच ड्रग्स कंट्रोलर जनरल ऑफ इंडिया यानि DGCI ने कोरोना के इलाज के लिए एक और दवाई के आपात इस्तेमाल की मंजूरी दे दी है... जायडस कैडिला की 'विराफिन' दवा को कोविड-19 के इलाज के लिए आपात इजाजत दे दी गई है... रिपोर्ट्स के मुताबिक दवा कंपनी जायडस का दावा है कि विराफिन के इस्तेमाल के बाद सात दिन में 91.15 फीसदी कोरोना संक्रमितों का आरटी-पीसीआर टेस्ट निगेटिव आया है। इस एंटी वायरस दवा के इस्तेमाल से कोरोना मरीजों को राहत मिलती है और लड़ने की ताकत भी आती है। अगर कोरोना वायरस संक्रमित होने की शुरुआत में ही विराफिन दवा दी जाती है, तो मरीजों को बीमारी से उबरने में काफी मदद मिलेगी और तकलीफ भी कम होगी। हालांकि इस दवा को अभी डॉक्टर की सलाह के बाद ही दिया जाएगा और दवा अस्पतालों में ही मिलेगी... आपको बता दें कि कंपनी ने इस दवा का ट्रायल 25 केंद्रों पर किया था... जिसके नतीजे अच्छे रहे हैं...

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    Zydus Cadila की विराफिन दवा करेगी कोरोना दूर? DCGI ने इस्तेमाल के लिए दी मंजूरी

    oleh PunjabKesari TV| 195 dilihat

  • Bharat Biotech’s 'Covaxin' gets DCGI nod for phase 2, 3 clinical trials on children aged 2 to 18 yrs

    Bharat Biotech’s 'Covaxin' gets DCGI nod for phase 2, 3 clinical trials on children aged 2 to 18 yrs

    The Drugs Controller General of India (DCGI) on Thursday approved Phase 2 and 3 clinical trial of Bharat Biotech's COVAXIN vaccine in the age group of 2 to 18 years, informed the Ministry of Health and Family Welfare. Bharat Biotech will conduct trials in 525 healthy volunteers. "In the trial, the vaccine will be given by intramuscular route in two doses at day 0 and day 28," it said.

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    Bharat Biotech’s 'Covaxin' gets DCGI nod for phase 2, 3 clinical trials on children aged 2 to 18 yrs

    oleh The Economic Times| 190 dilihat

  • Corona Vaccination, पर DCGI ने दी मंजूरी अब बच्चों को लगेगा टीका

    Corona Vaccination, पर DCGI ने दी मंजूरी अब बच्चों को लगेगा टीका

    Corona Vaccination, पर DCGI ने दी मंजूरी अब बच्चों को लगेगा टीका

    #Chhattisgarh #MadhyaPradesh #INH24x7 #LiveNews #INH24x7Live

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    Corona Vaccination, पर DCGI ने दी मंजूरी अब बच्चों को लगेगा टीका

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  • बच्चों को भी लगेगा Corona Vaccine, DCGI ने Covaxin लगाने की दी मंजूरी

    बच्चों को भी लगेगा Corona Vaccine, DCGI ने Covaxin लगाने की दी मंजूरी

    बच्चों को भी लगेगा Corona Vaccine, DCGI ने Covaxin लगाने की दी मंजूरी

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    बच्चों को भी लगेगा Corona Vaccine, DCGI ने Covaxin लगाने की दी मंजूरी

    oleh Inh News| 86 dilihat

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रूस की वैक्सीन का भारत में होगा ट्रायल, DCGI ने दी अनुमति

रूस की वैक्सीन का भारत में होगा ट्रायल, DCGI ने दी अनुमति

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  • License of fake medicine manufacturers cancelled | DCGI | CDSCO #shortsBerikutnya

    License of fake medicine manufacturers cancelled | DCGI | CDSCO #shorts

    #BJPLive #BJP

    License of fake medicine manufacturers cancelled | DCGI | CDSCO #shorts

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    License of fake medicine manufacturers cancelled | DCGI | CDSCO #shorts

    oleh Bharatiya Janata Party Delhi| 48 dilihat

  • DCGI | Digene Gel | Stop Consumption |

    DCGI | Digene Gel | Stop Consumption |

    If you also consume Digene Gel due to stomach upset, then stop doing so immediately. Now the Drugs Controller General of India has issued an advisory alert regarding the company's antacid syrup, Digene Gel. Along with this, patients have been advised to immediately stop the consumption of Digene gel prepared at the Goa plant.
    ............................
    #DigeneGel #stomachupset #DrugControllerGeneralofIndia #antacidsyrup #patients #Goaplant #himachalabhiabhi #analpatrwal
    ..................................................
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    DCGI | Digene Gel | Stop Consumption |

    oleh Himachal Abhi Abhi| 35 dilihat

  • DCGI / DRUG_ALERT / drug alert / Chlorpheniramine_Maleate

    DCGI / DRUG_ALERT / drug alert / Chlorpheniramine_Maleate

    The Drugs Controller General of India has issued a drug alert regarding cough syrup containing fixed combination of chlorpheniramine maleate and phenylephrine. Syrups containing these combinations are commonly used to treat cold, cough and flu. The Drugs Controller General of India issued a letter related to this to the states and union territories on December 18. It clearly states that FDC should not be used for children below 4 years.
    ...........................
    #Drugs_Controller_General_of_India #Drug_Alert #Chlorpheniramine_Maleate #Phenylephrine #FDC #Himachalabhiabhi
    ..................................................
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    DCGI / DRUG_ALERT / drug alert / Chlorpheniramine_Maleate

    oleh Himachal Abhi Abhi| 16 dilihat

  • DCGI accepts expert committee report to allow Covaxin jabs without clinical trial

    DCGI accepts expert committee report to allow Covaxin jabs without clinical trial

    DCGI accepts recommendations of Subject Expert Committee (SEC) to no longer administer Covaxin in 'clinical trial mode'. The SEC of Drugs Controller General of India (DCGI) on Wednesday recommended removing the "clinical trial mode" condition related to Bharat Biotech's Covaxin. This entails that the beneficiaries will not be required to sign a consent form to take the indigenous COVID-19 vaccine if the SEC recommendation is accepted by the country's top drugs regulator.

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    DCGI accepts expert committee report to allow Covaxin jabs without clinical trial

    oleh The Economic Times| 207 dilihat

  • Covid-19: DCGI extends shelf life of Covishield to 9 months from manufacturing date

    Covid-19: DCGI extends shelf life of Covishield to 9 months from manufacturing date

    India's drug regulator DCGI has extended the shelf life of Covishield, the Oxford-AstraZeneca COVID-19 vaccine, from six to nine months from its manufacturing date. In a letter to the Serum Institute of India, Drugs Controller General of India V G Somani said the SII is permitted to apply the shelf life of nine months to unlabelled vials available on hand.

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    Covid-19: DCGI extends shelf life of Covishield to 9 months from manufacturing date

    oleh The Economic Times| 176 dilihat

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