FIRST LACT

Main information

  • Trade name:
  • FIRST LACT 30 CAP
  • Dosage:
  • 500MG
  • Pharmaceutical form:
  • CAP
  • Composition:
  • 30
  • Medicine domain:
  • Humans
  • Medicine type:
  • Allopathic drug

Documents

Localization

  • Available in:
  • FIRST LACT 30 CAP
    India
  • Language:
  • English

Other information

Status

  • Source:
  • Central Drugs Standard Control Organization
  • Last update:
  • 09-08-2016

20-4-2018

FDA authorizes new use of test, first to identify the emerging pathogen <i>Candida auris</i>

FDA authorizes new use of test, first to identify the emerging pathogen <i>Candida auris</i>

FDA authorized the first test to identify the emerging pathogen Candida auris, which can cause serious infections in hospitalized patients.

FDA - U.S. Food and Drug Administration

17-4-2018

FDA approves first therapy for rare inherited form of rickets, x-linked hypophosphatemia

FDA approves first therapy for rare inherited form of rickets, x-linked hypophosphatemia

FDA approved Crysvita (burosumab), the first drug approved to treat adults and children ages 1 year and older with x-linked hypophosphatemia (XLH), a rare form of rickets.

FDA - U.S. Food and Drug Administration

11-4-2018

FDA permits marketing of artificial intelligence-based device to detect certain diabetes-related eye problems

FDA permits marketing of artificial intelligence-based device to detect certain diabetes-related eye problems

FDA permits marketing of first medical device to use artificial intelligence to detect greater than a mild level of diabetic retinopathy in the eye of adults who have diabetes.

FDA - U.S. Food and Drug Administration

10-4-2018

FDA clears first contact lens with light-adaptive technology

FDA clears first contact lens with light-adaptive technology

FDA clears first contact lens with additive that automatically darkens the lens when exposed to bright light

FDA - U.S. Food and Drug Administration

3-4-2018

FDA Orders Mandatory Recall for Kratom Products Due to Risk of <em>Salmonella</em>

FDA Orders Mandatory Recall for Kratom Products Due to Risk of <em>Salmonella</em>

Today, the U.S. Food and Drug Administration announced it has issued a mandatory recall order for all food products containing powdered kratom manufactured, processed, packed, or held by Triangle Pharmanaturals LLC, after several were found to contain salmonella. The agency took this action after the company failed to cooperate with the FDA’s request to conduct a voluntary recall. This is the first time the agency has issued a mandatory recall order to protect Americans from contaminated food products.

FDA - U.S. Food and Drug Administration

3-4-2018

FDA orders mandatory recall for kratom products due to risk of salmonella

FDA orders mandatory recall for kratom products due to risk of salmonella

Today, the U.S. Food and Drug Administration announced it has issued a mandatory recall order for all food products containing powdered kratom manufactured, processed, packed, or held by Triangle Pharmanaturals LLC, after several were found to contain salmonella. The agency took this action after the company failed to cooperate with the FDA’s request to conduct a voluntary recall. This is the first time the agency has issued a mandatory recall order to protect Americans from contaminated food products.

FDA - U.S. Food and Drug Administration

28-3-2018

First Source Issues Allergy Alert on Undeclared Peanuts in Wegmans 9 Oz Yogurt Raisins

First Source Issues Allergy Alert on Undeclared Peanuts in Wegmans 9 Oz Yogurt Raisins

First Source of Tonawanda, NY, is voluntarily recalling 9 OZ packages of Wegmans Yogurt Raisins, because the product may contain undeclared peanuts. People who have an allergy or sensitivity to peanuts run the risk of serious or life- threatening allergic reaction if they consume this product.

FDA - U.S. Food and Drug Administration

27-3-2018

FDA authorizes first fully interoperable continuous glucose monitoring system, streamlines review pathway for similar devices

FDA authorizes first fully interoperable continuous glucose monitoring system, streamlines review pathway for similar devices

The authorization classifies integrated continuous glucose monitoring devices in class II and subjects them to certain criteria called special controls

FDA - U.S. Food and Drug Administration

20-3-2018

FDA expands approval of Adcetris for first-line treatment of Stage III or IV classical Hodgkin lymphoma in combination with chemotherapy

FDA expands approval of Adcetris for first-line treatment of Stage III or IV classical Hodgkin lymphoma in combination with chemotherapy

FDA approves Adcetris (brentuximab vedotin) to treat adult patients with previously untreated stage III or IV classical Hodgkin lymphoma (cHL) in combination with chemotherapy

FDA - U.S. Food and Drug Administration

20-3-2018

Medicines Safety Update, Volume 9, Number 1, February-March 2018

Medicines Safety Update, Volume 9, Number 1, February-March 2018

First-generation oral sedating antihistamines – use in children, Suvorexant (Belsomra) – next day effects, Desvenlafaxine (Pristiq) recommended dose, Miconazole and potential interaction with warfarin

Therapeutic Goods Administration - Australia

19-3-2018

Scientific guideline:  Guideline on good pharmacogenomic practice - First version, adopted

Scientific guideline: Guideline on good pharmacogenomic practice - First version, adopted

This guideline provides recommendations for the conduct of genomic studies in relation to medical therapy in order to provide high quality information on the impact of genomic variability on drug response. Primary focus is on the analysis of genomic germline DNA. The analysis of somatic DNA and genomic biomarkers for cancer treatment is not being discussed and might be developed as an Annex or in separate guidance.

Europe - EFSA - European Food Safety Authority EFSA Journal

7-3-2018

National Research Programme for Environmental and Occupational Health: 36 projects selected and €6.3 million mobilised for the 2017 calls for projects

National Research Programme for Environmental and Occupational Health: 36 projects selected and €6.3 million mobilised for the 2017 calls for projects

Today, ANSES is publishing the list of projects selected as part of its three 2017 calls for research projects for the National Research Programme for Environmental and Occupational Health: the first for projects on a general theme, the second on the theme of "Radiofrequencies and health" and the third on the theme of "Antimicrobial resistance and the environment". Following the selection process, 36 projects are being supported with funding amounting to a total of 6.3 million euros. Language English

France - Agence Nationale du Médicament Vétérinaire

7-3-2018

FDA approves first tests to screen for tickborne parasite in whole blood and plasma to protect the U.S. blood supply

FDA approves first tests to screen for tickborne parasite in whole blood and plasma to protect the U.S. blood supply

FDA approves first tests to screen for tickborne parasite in blood donations

FDA - U.S. Food and Drug Administration

25-4-2018

Injured U.S. Vet Receives World's First Penis/Scrotum Transplant

Injured U.S. Vet Receives World's First Penis/Scrotum Transplant

Title: Injured U.S. Vet Receives World's First Penis/Scrotum TransplantCategory: Health NewsCreated: 4/23/2018 12:00:00 AMLast Editorial Review: 4/24/2018 12:00:00 AM

US - MedicineNet

25-4-2018

FIRST AID ANTISEPTIC (Povidone-Iodine) Solution [Target Corporation]

FIRST AID ANTISEPTIC (Povidone-Iodine) Solution [Target Corporation]

Updated Date: Apr 25, 2018 EST

US - DailyMed

24-4-2018

Ask the First Signs of Rheumatoid Arthritis

Ask the First Signs of Rheumatoid Arthritis

What Are the First Signs of Rheumatoid Arthritis?

US - eMedicineHealth

23-4-2018

Ask the First Signs of Psoriatic Arthritis

Ask the First Signs of Psoriatic Arthritis

What Are the First Signs of Psoriatic Arthritis?

US - eMedicineHealth

23-4-2018

FIRST AID ONLY STING RELIEF (Benzocaine) Swab [Acme United Corporation]

FIRST AID ONLY STING RELIEF (Benzocaine) Swab [Acme United Corporation]

Updated Date: Apr 23, 2018 EST

US - DailyMed

23-4-2018

FIRST AID ANTISEPTIC (Povidone-Iodine) Solution [Topco Associates LLC]

FIRST AID ANTISEPTIC (Povidone-Iodine) Solution [Topco Associates LLC]

Updated Date: Apr 23, 2018 EST

US - DailyMed

20-4-2018

First Drug for Rare Form of Rickets Approved by FDA

First Drug for Rare Form of Rickets Approved by FDA

Title: First Drug for Rare Form of Rickets Approved by FDACategory: Health NewsCreated: 4/18/2018 12:00:00 AMLast Editorial Review: 4/19/2018 12:00:00 AM

US - MedicineNet

19-4-2018

French Man First in World to Have Second Face Transplant

French Man First in World to Have Second Face Transplant

Title: French Man First in World to Have Second Face TransplantCategory: Health NewsCreated: 4/17/2018 12:00:00 AMLast Editorial Review: 4/18/2018 12:00:00 AM

US - MedicineNet

19-4-2018

FIRST AID ANTISEPTIC (Povidone-Iodine) Solution [Dolgencorp LLC]

FIRST AID ANTISEPTIC (Povidone-Iodine) Solution [Dolgencorp LLC]

Updated Date: Apr 19, 2018 EST

US - DailyMed

16-4-2018

Provisional approval pathway - first determination decision

Provisional approval pathway - first determination decision

First medicine to be granted a provisional approval determination

Therapeutic Goods Administration - Australia

14-4-2018

Doctors Curbing First-Time Prescriptions for Opioids

Doctors Curbing First-Time Prescriptions for Opioids

Title: Doctors Curbing First-Time Prescriptions for OpioidsCategory: Health NewsCreated: 4/12/2018 12:00:00 AMLast Editorial Review: 4/13/2018 12:00:00 AM

US - MedicineNet

12-4-2018

First Auto-Darken Contact Lenses Approved

First Auto-Darken Contact Lenses Approved

Title: First Auto-Darken Contact Lenses ApprovedCategory: Health NewsCreated: 4/10/2018 12:00:00 AMLast Editorial Review: 4/11/2018 12:00:00 AM

US - MedicineNet

12-4-2018

FDA OKs AI Device to Detect Diabetic Retinopathy

FDA OKs AI Device to Detect Diabetic Retinopathy

The FDA has approved the first medical device that uses artificial intelligence (AI) software to detect diabetic retinopathy in adults with diabetes that can be used by non-eye care professionals.

US - RxList

11-4-2018

#ICYMI FDA permits marketing of the first medical device to use artificial intelligence to detect greater than a mild level of diabetic retinopathy in the eye of adults who have diabetes.  http://go.usa.gov/xQTE2  #Diabetes #ArtificialIntelligence #AI #Me

#ICYMI FDA permits marketing of the first medical device to use artificial intelligence to detect greater than a mild level of diabetic retinopathy in the eye of adults who have diabetes. http://go.usa.gov/xQTE2  #Diabetes #ArtificialIntelligence #AI #Me

#ICYMI FDA permits marketing of the first medical device to use artificial intelligence to detect greater than a mild level of diabetic retinopathy in the eye of adults who have diabetes. http://go.usa.gov/xQTE2  #Diabetes #ArtificialIntelligence #AI #MedicalDevice pic.twitter.com/kpQyicVEWM

FDA - U.S. Food and Drug Administration

11-4-2018

FDA permits marketing of the first medical device to use artificial intelligence to detect greater than a mild level of diabetic retinopathy in the eye of adults who have diabetes.  https://go.usa.gov/xQTE2  #Diabetes #ArtificialIntelligence #AI #MedicalD

FDA permits marketing of the first medical device to use artificial intelligence to detect greater than a mild level of diabetic retinopathy in the eye of adults who have diabetes. https://go.usa.gov/xQTE2  #Diabetes #ArtificialIntelligence #AI #MedicalD

FDA permits marketing of the first medical device to use artificial intelligence to detect greater than a mild level of diabetic retinopathy in the eye of adults who have diabetes. https://go.usa.gov/xQTE2  #Diabetes #ArtificialIntelligence #AI #MedicalDevice

FDA - U.S. Food and Drug Administration

11-4-2018

FDA OKs First Transitional Contacts That Darken in Sunlight

FDA OKs First Transitional Contacts That Darken in Sunlight

The first contact lenses that have an additive that automatically darkens the lenses when exposed to bright light have been cleared by the US Food and Drug Administration (FDA).

US - RxList

11-4-2018

First Transitional Contacts That Darken in the Sun

First Transitional Contacts That Darken in the Sun

FDA OKs First Transitional Contacts That Darken in Sunlight

US - eMedicineHealth

10-4-2018

England's Scarlet Fever Cases Highest in 36 Years

England's Scarlet Fever Cases Highest in 36 Years

An outbreak of scarlet fever in England and Wales has seen the highest number of cases reported in the first quarter of a year since Public Health England (PHE) began collecting data in 1982.

US - RxList

6-4-2018

Scientific guideline:  Draft addendum to the guideline on the evaluation of medicinal products indicated for treatment of bacterial infections to address paediatric-specific clinical data requirements - First version, draft: consultation open

Scientific guideline: Draft addendum to the guideline on the evaluation of medicinal products indicated for treatment of bacterial infections to address paediatric-specific clinical data requirements - First version, draft: consultation open

This document proposes the development of an addendum to the Guideline on the evaluation of medicines indicated for treatment of bacterial infections CPMP/EWP/558/95 rev 2), to provide specific guidance on paediatric clinical development programmes to support the authorisation of antibacterial agents for treating infectious diseases in children.

Europe - EMA - European Medicines Agency

29-3-2018

Michelle Tarver, MD, PhD. - Ophthalmologist and Epidemiologist here at the FDA’s Center for Devices and Radiological Health,  organized the first Patient Engagement Advisory Committee (PEAC) Meeting as Acting Assistant Director of Strategic Programs, CDRH

Michelle Tarver, MD, PhD. - Ophthalmologist and Epidemiologist here at the FDA’s Center for Devices and Radiological Health, organized the first Patient Engagement Advisory Committee (PEAC) Meeting as Acting Assistant Director of Strategic Programs, CDRH

Michelle Tarver, MD, PhD. - Ophthalmologist and Epidemiologist here at the FDA’s Center for Devices and Radiological Health, organized the first Patient Engagement Advisory Committee (PEAC) Meeting as Acting Assistant Director of Strategic Programs, CDRH #WomensHistoryMonth pic.twitter.com/ZlMfKbdayV

FDA - U.S. Food and Drug Administration

29-3-2018

FIRST AID ONLY ANTACID (Calcium Carbonate) Tablet, Chewable [Acme United Corporation]

FIRST AID ONLY ANTACID (Calcium Carbonate) Tablet, Chewable [Acme United Corporation]

Updated Date: Mar 29, 2018 EST

US - DailyMed

28-3-2018

FIRST AID ONLY ASPIRIN (Aspirin) Tablet, Film Coated [Acme United Corporation]

FIRST AID ONLY ASPIRIN (Aspirin) Tablet, Film Coated [Acme United Corporation]

Updated Date: Mar 28, 2018 EST

US - DailyMed

27-3-2018

Embolization Procedure Reduces Osteoarthritis Knee Pain

Embolization Procedure Reduces Osteoarthritis Knee Pain

A minimally invasive, image-guided procedure that blocks small vessels in the knee with the help of biodegradable microspheres relieves symptoms of knee osteoarthritis (OA), a small study found. In the first US clinical trial of geniculate artery embolization (GAE), the procedure provided durable results out to 6 months in 6 of 13 patients tested.

US - RxList

26-3-2018

FIRST AID ONLY IBUPROFEN (Ibuprofen) Tablet, Coated [Acme United Corporation]

FIRST AID ONLY IBUPROFEN (Ibuprofen) Tablet, Coated [Acme United Corporation]

Updated Date: Mar 26, 2018 EST

US - DailyMed

16-3-2018

FDA to Lower Nicotine in Cigarettes to 'Nonaddictive' Levels

FDA to Lower Nicotine in Cigarettes to 'Nonaddictive' Levels

The US Food and Drug Administration (FDA) is taking what it calls a historic first step toward eliminating cigarettes' addictive properties by seeking comments on the impact of lower nicotine levels, how lowering of nicotine levels might be accomplished, and whether doing so might have unintended consequences.

US - RxList

16-3-2018

Ask Where Does Prostate Cancer Spread to First

Ask Where Does Prostate Cancer Spread to First

Where Does Prostate Cancer Spread to First?

US - eMedicineHealth

9-3-2018

First Screening Tests Approved for Tickborne Parasite

First Screening Tests Approved for Tickborne Parasite

Title: First Screening Tests Approved for Tickborne ParasiteCategory: Health NewsCreated: 3/7/2018 12:00:00 AMLast Editorial Review: 3/8/2018 12:00:00 AM

US - MedicineNet

9-3-2018

Ask What Is the First Sign of Glaucoma

Ask What Is the First Sign of Glaucoma

What Is the First Sign of Glaucoma?

US - eMedicineHealth

8-3-2018

FDA Approves First Home Test for Breast Cancer Genes

FDA Approves First Home Test for Breast Cancer Genes

Title: FDA Approves First Home Test for Breast Cancer GenesCategory: Health NewsCreated: 3/6/2018 12:00:00 AMLast Editorial Review: 3/7/2018 12:00:00 AM

US - MedicineNet

8-3-2018

FIRST C WATERFALL (Niacinamide, Adenosine) Cream [LIZK Co., Ltd.]

FIRST C WATERFALL (Niacinamide, Adenosine) Cream [LIZK Co., Ltd.]

Updated Date: Mar 8, 2018 EST

US - DailyMed

6-3-2018

FIRST C SUPERFULL (Arbutin, Adenosine) Cream [LIZK Co., Ltd.]

FIRST C SUPERFULL (Arbutin, Adenosine) Cream [LIZK Co., Ltd.]

Updated Date: Mar 6, 2018 EST

US - DailyMed

1-3-2018

 Call for scientific data for use in HMPC assessment work on Ilex paraguariensis St. Hilaire, folium – Revision 1, draft: consultation open

Call for scientific data for use in HMPC assessment work on Ilex paraguariensis St. Hilaire, folium – Revision 1, draft: consultation open

The HMPC invites all interested parties such as pharmaceutical industry associations, health care professional groups, learned societies, consumers and patients’ associations, governmental institutions as well as EU and EEA-EFTA Member States to submit any scientific data that the HMPC should consider at the periodic review of the monograph on Hamamelis virginiana L., cortex towards a possible revision of the monograph and supporting documents. The publication of this call is the first step in the proced...

Europe - EMA - European Medicines Agency

1-3-2018

 Call for scientific data for use in HMPC assessment work on Hamamelis virginiana L., folium et cortex aut ramunculus destillatum – First version, draft: consultation open

Call for scientific data for use in HMPC assessment work on Hamamelis virginiana L., folium et cortex aut ramunculus destillatum – First version, draft: consultation open

The HMPC invites all interested parties such as pharmaceutical industry associations, health care professional groups, learned societies, consumers and patients’ associations, governmental institutions as well as EU and EEA-EFTA Member States to submit any scientific data that the HMPC should consider at the periodic review of the monograph on Hamamelis virginiana L., folium et cortex aut ramunculus destillatumtowards a possible revision of the monograph and supporting documents. The publication of this ...

Europe - EMA - European Medicines Agency

1-3-2018

 Call for scientific data for use in HMPC assessment work on Hamamelis virginiana L., folium – First version, draft: consultation open

Call for scientific data for use in HMPC assessment work on Hamamelis virginiana L., folium – First version, draft: consultation open

The HMPC invites all interested parties such as pharmaceutical industry associations, health care professional groups, learned societies, consumers and patients’ associations, governmental institutions as well as EU and EEA-EFTA Member States to submit any scientific data that the HMPC should consider at the periodic review of the monograph on Hamamelis virginiana L., folium towards a possible revision of the monograph and supporting documents. The publication of this call is the first step in the proced...

Europe - EMA - European Medicines Agency

1-3-2018

 Call for scientific data for use in HMPC assessment work on Hamamelis virginiana L., cortex – First version, draft: consultation open

Call for scientific data for use in HMPC assessment work on Hamamelis virginiana L., cortex – First version, draft: consultation open

The HMPC invites all interested parties such as pharmaceutical industry associations, health care professional groups, learned societies, consumers and patients’ associations, governmental institutions as well as EU and EEA-EFTA Member States to submit any scientific data that the HMPC should consider at the periodic review of the monograph on Hamamelis virginiana L., cortex towards a possible revision of the monograph and supporting documents. The publication of this call is the first step in the proced...

Europe - EMA - European Medicines Agency