https://thehealthmaster.com/?p=40196
Sunday, July 31, 2022
How to Control Stress
आज के दौर में तनाव यानी स्ट्रेस जिंदगी का हिस्सा बन गया है. पर्सनल से लेकर प्रोफेशनल लाइफ में लोगों को तनाव का सामना करना पड़ता है. तनाव के दौरान आप उदास या चिंतित महसूस कर सकते हैं.
यह कुछ समय के लिए सामान्य माना जाता है, लेकिन अगर तनाव ज्यादा बढ़ जाए, तो यह कई गंभीर बीमारियों की वजह बन सकता है और मेंटल हेल्थ को बुरी तरह प्रभावित कर सकता है.
तनाव को कंट्रोल करने के लिए आप अपनी जिंदगी में कुछ छोटी-छोटी बातों का ध्यान रख सकते हैं. इस बारे में विस्तार से जान लेते हैं.
Click for more on Stress
तनाव को कैसे कर सकते हैं कंट्रोल?
वेबएमडी की रिपोर्ट के मुताबिक तनाव को कंट्रोल करने के लिए आपको कुछ बातों का ध्यान रखना होगा. सबसे पहले आपको चीजों को लेकर पॉजिटिव एटिट्यूड रखना होगा.
जिन घटनाओं को आप कंट्रोल नहीं कर सकते, उनके बारे में ज्यादा नहीं सोचना चाहिए. तनावपूर्ण परिस्थितियों में आक्रामक होने के बजाय मुखर रहें. अपनी भावनाओं को कंट्रोल करना सीखें और समय का प्रभावी ढंग से इस्तेमाल करें.
आप उन चीजों की पहचान करें, जिनसे आपको सबसे ज्यादा स्ट्रेस होता है. तनाव कम करने के लिए शराब, ड्रग्स या अन्य खतरनाक चीजों पर बिलकुल भरोसा न करें. ड्रग्स और अल्कोहल आपके शरीर को गंभीर तनाव दे सकते हैं.
उन लोगों के साथ पर्याप्त समय बिताएं जिन्हें आप प्यार करते हैं. अगर फिर भी परेशानी कम नहीं हो रही, तो मनोवैज्ञानिक या अन्य मानसिक स्वास्थ्य पेशेवर से कंसल्ट कर सकते हैं.
एक्सरसाइज और हेल्दी डाइट से कम होता है तनाव
एक्सरसाइज और अन्य फिजिकल एक्टिविटी आपकी नींद को बेहतर बनाने में मदद कर सकती हैं. इससे तनाव को बेहतर तरीके से मैनेज किया जा सकता है.
कई स्टडी में यह बात सामने आ चुकी है कि हर दिन एक्सरसाइज करना मेंटल हेल्थ के लिए बेहद फायदेमंद होता है. इससे स्ट्रेस को कम करने में मदद मिलती है.
रनिंग, स्विमिंग, साइकलिंग, डांसिंग से तनाव को काफी हद तक कम किया जा सकता है. खान-पान का स्ट्रेस पर काफी असर पड़ता है.
हेल्दी डाइट लेने से तनाव के प्रभाव को कम किया जा सकता है. हेल्दी डाइट से इम्यूनिटी मजबूत होती है और मूड बेहतर होता है.
तनाव को कम करने के लिए विटामिन सी, मैग्नीशियन और ओमेगा 3 फैटी एसिड से भरपूर पदार्थ डाइट में शामिल करने चाहिए.
प्रॉपर नींद लेना बेहद जरूरी
तनाव का एक साइड इफेक्ट यह है कि आपको नींद नहीं आती. नींद की कमी आपके तनाव के स्तर को भी बढ़ा सकती है. इसलिए हर किसी को हर दिन 7 से 8 घंटे की नींद लेनी चाहिए.
अच्छी नींद में आपके बेडरूम की भूमिका भी महत्वपूर्ण है. सामान्य तौर पर आपका कमरा शांत और ठंडा होना चाहिए. आपका बिस्तर साफ और आरामदायक होना चाहिए.
देर रात तक जागना तनाव के लेवल को बिगाड़ सकता है. इसलिए आपको सोने का समय फिक्स करना चाहिए.
Coffee: कॉफी पीने के शौकीन हो जाएं सावधान, Let’s know the problems
Cosmetic Surgery Part 2: बेहतर लुक के लिए कॉस्मेटिक सर्जरी: Let’s know all about
High BP: The amount of water you should drink to reduce…
Heart attack: Study says this shower habit could lead to a heart attack
These 5 Health check-ups everyone needs to undergo
Mental Health Guide: Signs that you need immediate Medical Help
Toilet में मोबाइल का इस्तेमाल: हो सकते है ये गंभीर परिणाम – Must read
Sustainable Skincare products: Part 1
These Checkups and Tests you shouldn’t miss
These two Vitamin deficiencies can lead to vision loss
https://thehealthmaster.com/2022/07/31/stress-%e0%a4%95-%e0%a4%b5%e0%a4%9c%e0%a4%b9-%e0%a4%b8-%e0%a4%b0%e0%a4%b9%e0%a4%a4-%e0%a4%b9-problems-%e0%a4%a4-%e0%a4%90%e0%a4%b8-%e0%a4%95%e0%a4%b0-stress-control/
New technology that deactivates COVID-19 virus in just 1 minute
New technology that deactivates COVID-19 virus in just 1 minute
https://thehealthmaster.com/?p=40168
Saturday, July 30, 2022
New technology that deactivates COVID-19 virus in just 1 minute
New technology that deactivates COVID-19 virus in just 1 minute
https://thehealthmaster.com/?p=40168
Medical Device Alert: Lists
Download the Medical Device Alert lists link is given below:
https://thehealthmaster.com/medical-device-alert-lists/
New technology that deactivates COVID-19 virus in just 1 minute
New technology that deactivates COVID-19 virus in just 1 minute
https://thehealthmaster.com/?p=40168
High BP: The amount of water you should drink to reduce blood pressure
High BP: The amount of water you should drink to reduce blood pressure
https://thehealthmaster.com/?p=39409
Friday, July 29, 2022
Download the Medical Device Alert lists link is given below: We have provided the list of Medical Device Alert announced by DCGI.
Picture: Pixabay
Medical Device Alert lists
2022
Download Medical Device Alert 21-07-2022, click below link
Medical-Device-Alert-21-07-2022
Download Medical Device Alert 21-06-2022, click below link
Medical-Device-Alert-21-06-2022
Download Medical Device Alert 14-06-2022, click below link
Medical-Device-Alert-14-06-2022
2021
Download Medical Device Alert 08-11-2021, click below link
Medical-Device-Alert-08-11-2021
Download Medical Device Alert 11-10-2021, click below link
Medical-Device-Alert-11-10-2021
Download Medical Device Alert 09-08-2021, click below link
Medical-Device-Alert-09-08-2021
2019
Download Medical Device Alert 20-05-2019, click below link
Medical-Device-Alert-20-05-2019
Download Medical Device Alert January 2019, click below link
Medical-Device-Alert-January-2019
Source of Drug alert lists: CDSCO website
Commercial Testing Laboratories
Govt Laboratories
List of Laboratory instruments
Latest Notifications: Testing Laboratories
https://thehealthmaster.com/medical-device-alert-lists/
Download the Medical Device Alert lists link is given below: We have provided the list of Medical Device Alert announced by DCGI.
Picture: Pixabay
Medical Device Alert lists
2022
Download Medical Device Alert 21-07-2022, click below link
Medical-Device-Alert-21-07-2022
Download Medical Device Alert 21-06-2022, click below link
Medical-Device-Alert-21-06-2022
Download Medical Device Alert 14-06-2022, click below link
Medical-Device-Alert-14-06-2022
2021
Download Medical Device Alert 08-11-2021, click below link
Medical-Device-Alert-08-11-2021
Download Medical Device Alert 11-10-2021, click below link
Medical-Device-Alert-11-10-2021
Download Medical Device Alert 09-08-2021, click below link
Medical-Device-Alert-09-08-2021
2019
Download Medical Device Alert 20-05-2019, click below link
Medical-Device-Alert-20-05-2019
Download Medical Device Alert January 2019, click below link
Medical-Device-Alert-January-2019
Source of Drug alert lists: CDSCO website
Also read, click below link
Drug Alert: NSQ DRugs List
Commercial Testing Laboratories
Govt Laboratories
List of Laboratory instruments
Latest Notifications: Testing Laboratories
Click to read other articles of the Author
Licensing procedure for Medical devices
Latest Notifications: Medical Devices
Classifications of Medical Devices under the provisions of MDR 2017
FAQs on Medical Devices Rules, 2017
FAQs – on Blood Pressure Monitoring Devices
FAQs – on Blood Bags and its Testing
https://thehealthmaster.com/2022/07/10/medical-device-alert-lists/
Download the Medical Device Alert lists link is given below: We have provided the list of Medical Device Alert announced by DCGI.
Picture: Pixabay
Medical Device Alert lists
2022
Medical Device Alert 21-07-2022, click below link
Medical-Device-Alert-21-07-2022
Download Medical Device Alert 21-06-2022, click below link
Medical-Device-Alert-21-06-2022
Download Medical Device Alert 14-06-2022, click below link
Medical-Device-Alert-14-06-2022
2021
Download Medical Device Alert 08-11-2021, click below link
Medical-Device-Alert-08-11-2021
Download Medical Device Alert 11-10-2021, click below link
Medical-Device-Alert-11-10-2021
Download Medical Device Alert 09-08-2021, click below link
Medical-Device-Alert-09-08-2021
2019
Download Medical Device Alert 20-05-2019, click below link
Medical-Device-Alert-20-05-2019
Download Medical Device Alert January 2019, click below link
Medical-Device-Alert-January-2019
Source of Drug alert lists: CDSCO website
Commercial Testing Laboratories
Govt Laboratories
List of Laboratory instruments
Latest Notifications: Testing Laboratories
https://thehealthmaster.com/medical-device-alert-lists/
High BP: The amount of water you should drink to reduce blood pressure
High BP: The amount of water you should drink to reduce blood pressure
https://thehealthmaster.com/?p=39409
Thursday, July 28, 2022
Hyderabad: Hyderabad-based Zenara Pharma, a fully owned subsidiary of Biophore India Pharmaceuticals, on Thursday said it has received emergency use authorization (EUA) from the Central Drugs Standard Control Organization (CDSCO) to manufacture and market in India a generic version of Pfizer’s Covid-19 pill Paxlovid for the treatment of patients with mild to moderate Covid-19 symptoms.
The approval is for Nirmatrelvir and Ritonavir tablets in a combi pack and they will be sold under the Paxzen brand in India. The drug is being manufactured at Zenara’s USFDA-approved facility in Hyderabad.
Pointing out that the company was one of the first companies to bring the drug to market in India in record time, Zenara Pharma co-founder & managing director Jagadeesh Babu Rangisetty said the company has its own in-house active pharmaceutical ingredients pipeline for the drug and was not dependent on imports for production of the drug.
“This will ensure stability and rapid production and availability of this treatment for the Indian market,” he said.
The breakthrough approval in the US for Paxlovid was given by the USFDA in Dec 2021. It was the first oral pill that has been approved by USFDA and is claimed to have a better safety profile than subsequently approved oral therapies.
Zenara Pharma CEO Dr. Srinivas Arutla said the company expects to launch Paxzen in the next couple of weeks and is in talks with multiple institutions and hospitals in the country to ensure ready availability for patients in need.
Source link
https://thehealthmaster.com/2022/07/28/cdsco-gives-nod-to-make-generic-version-of-pfizers-covid-19-pill/
Apply online, link is given below: USP is proud to be an equal opportunity/affirmative action employer.
Employment selection and related decisions are made without regard to sex, gender identity, race, age, disability, religion, national origin, color, veteran status, or any other protected class.
We are committed to working with and providing reasonable accommodation to individuals with disabilities.
Post: Scientist III- RSE
Summary of the PositionThis is a non-supervisory position in the Reference Standard Evaluation department, responsible for oversight and successful implementation and completion of all activities pertaining to a portfolio of Reference Standards (RS), Pharmaceutical Analytical Impurities (PAI) and Certified Reference Materials (CRMs) or any other physical materials USP intend to develop. The position is expected to contribute majorly to PAI activities.
It is more of an operational and tactical role. This incumbent is responsible for, including but not limited to, timely preparation of procurement specifications, collaborative testing protocols for RS, APIs, and CRMs, providing technical assistance for collaborating labs, analytical data review, preparation of scientific/technical reports, Certificates, Product Information Sheet (PIS), defining and preparation of packaging configuration, Quality Control testing instructions, resolving technical issues.
Job Description
• Responsible for managing the development of PAIs by working in collaboration with internal and external stakeholders/partners as necessary
• Item creation, reviewing the data package from partners, preparation of packaging and labeling forms (PLF)
• Preparing the documentation including, but not limited to, the test protocol, PAI report, and product information sheet.
• Communicate with internal stakeholders and external partners as and when required
• Addressing customer queries and complaints promptly after doing necessary investigation
• To have the ability to do “Problem-solving” at any step of the development process Contribution to regular Reference Standard development process as and when required, that involves
• Responsible for timely preparation of procurement specifications and collaborative testing protocols for new/replacement RS lots, technical assistance for collaborating labs
• To review the analytical data received from the collaborators and to prepare summary reports and Reference Standard Candidate Evaluation Package (RSCEP), preparation of packaging and QC testing instructions, and assign periodic re-test intervals.
Independently maintains successful scheduling operations, necessary documents, and complete and accurate information; and addresses quality issues to ensure availability of reference standards in a complex portfolio.
• To have a discussion with Scientific Liaison (SL) and Expert Committee (EC) members during new monograph or monograph modernization processes. Participating in peer review of draft monograph before submission to Pubs.
• To Draft product planning documents (PPD), coordinate with labs, and review/interprets data from international collaborative studies.
• Submits collaborative study summary reports to review and subsequent approval for each RS lot. Addresses the concerns of balloters to achieve successful approval of RSCEPs.
• To have the ability to do “Problem-solving” at any step of the RS development process.
• To produce quality documents (RSCEP, Addenda, TP) with minimum comments from RSTO and no “Major” observation from QA.
• To Coordinates for any additional necessary testing and assist other staff members in addressing the comments.
• To provide correct guidance on the interpretation of test data, Propose and design studies to obtain necessary data to resolve complaints.
• To demonstrate technical understanding to internal and external audiences regarding USP's Reference Standards program.
• Engages in conversation about reference standards issues. Addresses general customer technical inquiries and thoroughly investigates customer complaints with minimal guidance.
• Performs and participates in other related duties as assigned.
Candidate Profile• Ph.D. in Chemistry / Pharmacy from a recognized University. Minimum of 0-2 years of Pharmaceutical industry experience
• MSc / MPharm from a recognized University. Minimum 7-8 years of Pharmaceutical industry experience Preferred Qualifications
• Prior knowledge of working with and/or qualifying reference materials
• Adequate laboratory experience to handle sophisticated analytical equipment
• Ability to read and interpret spectroscopic analyses data (NMR, IR, MS)
• Ability to handle multiple priorities in a fast-paced environment.
• Excellent written and verbal communication skills.
• Ability to operate independently where appropriate, yet understand when to escalate issues and how to establish effective working relationships
• Project Management skills. Must have the ability to prioritize and manage multiple, concurrent projects in a fast-paced and high-volume environment with changing deadlines and priorities
• Able to work flexible hours when needed to meet the project timelines
• Strong skills in troubleshooting, and solving technical problems
• Experience with, and knowledge of the USP-NF is preferred.
• Basic knowledge/familiarity with statistical analysis
Additional InformationExperience : 0 to 8 yearsQualification: Ph.D, M.Sc, M.Pharm
Location: HyderabadIndustry Type : Pharma / Healthcare / Clinical researchFunctional Area: RSE
End Date: 30th August 2022
Apply Online
Govt Job: for the post of Pharmacist at ECHS
Govt Job: For Ph.D, M.Pharm, MS Pharm at NIPER – Salary Rs. 65,000 pm
Govt Job; For Pharmacy Professionals at NDTL | Salary Rs 2 lakh pm
Govt Job: For Pharmacist under Deputy Director Health Services
Govt Job: For Life Sciences, Pharma Sciences Candidates at NIPER – – Salary upto Rs. 1,00,000 pm
Govt Job: For M.Pharm, M.Tech at research at PGIMER
https://thehealthmaster.com/2022/07/28/govt-job-for-ph-d-m-pharm-m-sc-at-usp-united-states-pharmacopeia/
Apply online, link is given below: USP is proud to be an equal opportunity/affirmative action employer.
Employment selection and related decisions are made without regard to sex, gender identity, race, age, disability, religion, national origin, color, veteran status or any other protected class.
We are committed to working with and providing reasonable accommodation to individuals with disabilities.
Post: Scientist III- RSE
Summary of the PositionThis is a non-supervisory position in the Reference Standard Evaluation department, responsible for oversight and successful implementation and completion of all activities pertaining to a portfolio of Reference Standards (RS), Pharmaceutical Analytical Impurities (PAI) and Certified Reference Materials (CRMs) or any other physical materials USP intend to develop. The position is expected to contribute majorly to PAI activities.
It is more of an operational and tactical role. This incumbent is responsible for, including but not limited to, timely preparation of procurement specifications, collaborative testing protocols for RS, APIs, and CRMs, providing technical assistance for collaborating labs, analytical data review, preparation of scientific/technical reports, Certificates, Product Information Sheet (PIS), defining and preparation of packaging configuration, Quality Control testing instructions, resolving technical issues.
Job Description
• Responsible for managing the development of PAIs by working in collaboration with internal and external stakeholders/partners as necessary
• Item creation, reviewing the data package from partners, preparation of packaging and labeling forms (PLF)
• Preparing the documentation including, but not limited to, the test protocol, PAI report, and product information sheet.
• Communicate with internal stakeholders and external partners as and when required
• Addressing customer queries and complaints promptly after doing necessary investigation
• To have the ability to do “Problem-solving” at any step of the development process Contribution to regular Reference Standard development process as and when required, that involves
• Responsible for timely preparation of procurement specifications and collaborative testing protocols for new/replacement RS lots, technical assistance for collaborating labs
• To review the analytical data received from the Collaborators and to prepare summary reports and Reference Standard Candidate Evaluation Package (RSCEP), preparation of packaging and QC testing instructions, and assign periodic re-test intervals. Independently maintains successful scheduling operations, necessary documents, and complete and accurate information; and addresses quality issues to ensure availability of reference standards in a complex portfolio.
• To have a discussion with Scientific Liaison (SL) and Expert Committee (EC) members during new monograph or monograph modernization processes. Participating in peer review of draft monograph before submission to Pubs.
• To Draft product planning documents (PPD), coordinate with labs, and review/interprets data from international collaborative studies.
• Submits collaborative study summary reports to review and subsequent approval for each RS lot. Addresses the concerns of balloters to achieve successful approval of RSCEPs.
• To have the ability to do “Problem-solving” at any step of the RS development process.
• To produce quality documents (RSCEP, Addenda, TP) with minimum comments from RSTO and no “Major” observation from QA.
• To Coordinates for any additional necessary testing and assist other staff members in addressing the comments.
• To provide correct guidance on the interpretation of test data, Propose and design studies to obtain necessary data to resolve complaints.
• To demonstrate technical understanding to internal and external audiences regarding USP's Reference Standards program.
• Engages in conversation about reference standards issues. Addresses general customer technical inquiries and thoroughly investigates customer complaints with minimal guidance.
• Performs and participates in other related duties as assigned.
Candidate Profile• Ph.D. in Chemistry / Pharmacy from a recognized University. Minimum of 0-2 years of Pharmaceutical industry experience
• MSc / MPharm from a recognized University. Minimum 7-8 years of Pharmaceutical industry experience Preferred Qualifications
• Prior knowledge of working with and/or qualifying reference materials
• Adequate laboratory experience to handle sophisticated analytical equipment
• Ability to read and interpret spectroscopic analyses data (NMR, IR, MS)
• Ability to handle multiple priorities in a fast-paced environment.
• Excellent written and verbal communication skills.
• Ability to operate independently where appropriate, yet understand when to escalate issues and how to establish effective working relationships
• Project Management skills. Must have the ability to prioritize and manage multiple, concurrent projects in a fast-paced and high-volume environment with changing deadlines and priorities
• Able to work flexible hours when needed to meet the project timelines
• Strong skills in troubleshooting, and solving technical problems
• Experience with, and knowledge of the USP-NF is preferred.
• Basic knowledge/familiarity with statistical analysis
Additional InformationExperience : 0 to 8 yearsQualification: Ph.D, M.Sc, M.Pharm
Location: HyderabadIndustry Type : Pharma / Healthcare / Clinical researchFunctional Area: RSE
End Date: 30th August 2022
Apply Online
Govt Job: for the post of Pharmacist at ECHS
Govt Job: For Ph.D, M.Pharm, MS Pharm at NIPER – Salary Rs. 65,000 pm
Govt Job; For Pharmacy Professionals at NDTL | Salary Rs 2 lakh pm
Govt Job: For Pharmacist under Deputy Director Health Services
Govt Job: For Life Sciences, Pharma Sciences Candidates at NIPER – – Salary upto Rs. 1,00,000 pm
Govt Job: For M.Pharm, M.Tech at research at PGIMER
https://thehealthmaster.com/2022/07/28/govt-job-for-ph-d-m-pharm-m-sc-at-usp-united-states-pharmacopeia/
Wednesday, July 27, 2022
Smyrna, TN, Vi-Jon, LLC is expanding its voluntary recall to include all lots of Magnesium Citrate Saline Laxative Oral Solution Lemon Flavor, 10 FL OZ (296 mL) within expiry to the consumer level.
The recall was initiated after 3rd Party and Vi-Jon, LLC microbial testing identified the presence of Gluconacetobacter liquefaciens.
Risk Statement: Immunocompromised patients, who consume this product, may be at increased risk for invasive infections caused by Gluconacetobacter liquefaciens that could lead to serious, life-threatening adverse health consequences.
Click for more drugs recall
To date, Vi-Jon, LLC has received one report of an adverse reaction potentially related to this recall. Vi-Jon, LLC is in the process of investigating this report.
The product is used for relief of occasional constipation (irregularity) and generally produces bowel movements in ½ to 6 hours. The product is packaged in a 10 oz clear round plastic bottle.
The affected brands of Magnesium Citrate Laxative Oral Solution Lemon Flavor manufactured at Vi-Jon, LLC in Smyrna, TN is:
Affected BrandNDC #UPC #BEST CHOICE 10OZ LEMON MAG CIT63941-533-38070038200499CARE ONE 10OZ LEMON MAG CIT72476-001-38341520313226CARIBA 10OZ LEMON MAG CITRATE67860-166-38646702057012CRUZ BLANC 10OZ LEMON MAG CITN/A308697403082CVS 10OZ LEMON MAG CIT63868-929-38050428335178CVS 10OZ LEMON MAG CIT69842-983-38050428305942DISCOUNT DRUG MART 10OZ LEMON MAG CITRATE53943-166-38093351028205EQUALINE 10OZ LEMON MAG CIT41163-709-38041163500679EQUATE 10OZ LEMON MAG CIT SRP49035-506-38681131287142EXCHANGE SELECT 10OZ LEMON MAG CIT55301-166-38614299404205FAMILY WELLNESS 10OZ LEMON CITRATE55319-666-38032251580826GOOD SENSE 10OZ LEMON MAG CIT50804-166-38846036007374HARRIS TEETER 10OZ LEMON MAG CITRATE72036-002-38072036726124HEB 10OZ LEMON MAG CITRATE37808-769-38041220510863HEALTH MART 10OZ LEMON MAG CIT62011-0380-1052569142158KROGER 10OZ LEMON MAG CITRATE30142-899-38041260001826LEADER 10OZ LEMON MAG CIT70000-0424-1096295135541MAJOR 10OZ LEMON MAG CITRATE0904-6787-44309046787440MEIJER 10OZ LEMON MAG CIT41250-708-38713733459457PREMIER VALUE 10OZ LOW SOD LEM CIT68016-696-38840986035302PUBLIX 10OZ LEMON MAG CIT56062-266-38041415506732QUALITY CHOICE 10OZ LEMON MAG CIT63868-929-38635515901254REXALL 10OZ LEMON MAG CITRATE55910-183-38072785134188RITE AID 10OZ LEMON CITRATE11822-4330-2011822433006SIGNATURE CARE 10OZ LEMON MAG CIT21130-709-38321130779155SOUND BODY 10OZ LEMON MAG CIT50594-166-38072785114791SUNMARK 10OZ LEMON MAG CIT70677-0051-1010939908445SWAN 10OZ LEMON MAG CITRATE0869-0166-38072785134058TOPCARE 10OZ LEMON MAG CITRATE36800-709-38036800455290UP&UP 10OZ LEMON MAG CIT11673-708-38072785128835UP&UP 10OZ LEMON MAG CIT11673-666-38072785128835WALGREENS 10OZ LEMON MAG CIT0363-8166-38311917201603
This recall is being conducted with the knowledge of the U.S. Food and Drug Administration (USFDA).
Other drugs recall
Drug recall: Propofol Injectable Emulsion recalled due to this reason
Drug recall: Insulin Glargine Injection Pens recalled due to this reason
Drug recall: Morphine Sulfate 30 mg, 60 mg Extended Release Tablets recalled due to this reason
Drug recall: Over 6 lakh bottles of Blood Pressure treatment tablets recalled
Drug recall: 2.1 million doses of medicine recalled due to this reason
Drug recall: Over 10,000 bottles of generic Anti-depression Drug recalled
USFDA issues Form 483 for six observations to Granules Pharma
USFDA gives approval for this tablet to treat High BP
No extension in deadline for registration of Medical Devices
Drug recall: Sun Pharma, Glenmark recall products due to these manufacturing issues
Govt plans to reduce the prices of critical drugs on August 15
NDPS: Inter-state drug racket busted – Huge stock including Alprazolam, Buprenorphine seized
NPPA fixed ceiling prices of 890 formulations and retail price of 2023 new drugs: Govt
NMC directs State Medical Councils to take action against Quacks
FDA Haryana team raided, Codeine syrup recovered, FIR lodged
Latest Notifications regarding Pharmaceuticals
https://thehealthmaster.com/2022/07/27/drug-recall-magnesium-citrate-oral-solution-recalled-due-to-this-reason/
Subscribe to:
Posts (Atom)