NEUTROGENA

Κύριές Πληροφορίες

  • Εμπορική ονομασία:
  • NEUTROGENA T/GEL 5 MG/ML MED.SHAMP
  • Φαρμακολογική κατηγορία (ATC):
  • D11AC30
  • Δοσολογία:
  • 5 MG/ML
  • Φαρμακοτεχνική μορφή:
  • ΣΑΠΩΝ ΓΙΑ ΤΟ ΤΡΙΧΩΤΟ ΤΗΣ ΚΕΦΑΛΗΣ (ΣΑΜΠΟΥΑΝ)
  • Χρήση για:
  • Οι άνθρωποι
  • Τύπος φάρμακου:
  • αλλοπαθητική των ναρκωτικών

Έγγραφα

Εντοπισμός

  • Διατίθεται σε:
  • NEUTROGENA T/GEL 5 MG/ML MED.SHAMP
    Ελλάδα
  • Γλώσσα:
  • Ελληνικά

Θεραπευτικές πληροφορίες

  • Θεραπευτική περιοχή:
  • ΦΑΡΜΑΚΕΥΤΙΚΟ ΠΡΟΪΟΝ

Άλλες πληροφορίες

Κατάσταση

  • Πηγή:
  • Εθνικός Οργανισμός Φαρμάκων
  • τελευταία ενημέρωση:
  • 09-08-2016

φύλλο οδηγιών χρήσης

ΦΥΛΛΟ ΟΔΗΓΙΩΝ ΓΙΑ ΤΟ ΧΡΗΣΤΗ

1. ΠΕΡΙΓΡΑΦΗ ΤΟΥ ΦΑΡΜΑΚΕΥΤΙΚΟΥ ΠΡΟΪΟΝΤΟΣ

1.1. Oνομασία

  Neutrogena ®  T/Gel ®  

  Σαμπουάν 5 mg/ml

1.2  Σύνθεση

Δραστική ουσία: 5mg/ml εξευγενισμένης λιθανθρακόπισσας

                   Έκδοχα:  Macrogol  lauryl  ether  (4),  Sodium  lauryl  ether  sulphate, 

Cocodiethanolamide,  Cocamidopropyl  betaine,  Imidazolidinyl  urea,  Methyl 

parahydroxybenzoate  (E218),  Propyl  parahydroxybenzoate  (E216), 

Tetrasodium EDTA, Citric acid anhydrous, Fragrance Fugio 242156, Sodium 

chloride, purified water 

1.3 Φαρμακοτεχνική μορφή

Σάπων για το τριχωτό της κεφαλής (Σαμπουάν).

1.4 Περιεκτικότητα

5 mg/ml  εξευγενισμένης  λιθανθρακόπισσας  

1.5 Περιγραφή – συσκευασία

Ένα ημιδιαφανές, κεχριμπαρένιο διάλυμα σε   φιαλίδια (PET  ή  PETG) των 

15, 125 ή 250 ml. Πιθανότατα να μη διατίθενται όλες οι συσκευασίες στην 

αγορά.

1.6 Φαρμακοθεραπευτική κατηγορία

Φαρμακευτικά σαμπουάν

1.7 Υπεύθυνος άδειας κυκλοφορίας

              Johnson & Johnson Hellas

Αιγιαλείας & Επιδαύρου 4

Μαρούσι 151 25 Αθήνα

Τηλ.: 2106875750

1.8 Υπεύθυνος απoδέσμευσης παρτίδας:

   Johnson & Johnson Limited

               Foundation Park, Roxborough Way, Maidenhead SL6 3UG, 

               ΑΓΓΛΙΑ

2. ΤΙ   ΠΡΕΠΕΙ   ΝΑ   ΓΝΩΡΙΖΕΤΕ   ΓΙΑ   ΤΟ   ΦΑΡΜΑΚΟ   ΠΟΥ   ΣΑΣ 

ΧΟΡΗΓΗΣΕ Ο ΓΙΑΤΡΟΣ ΣΑΣ

2.1 Γενικές πληροφορίες

Το σαμπουάν  Neutrogena ®   T/Gel ®   περιέχει ένα δραστικό συστατικό για την 

αντιμετώπιση της πιτυρίδας και της σμηγματορροϊκής δερματίτιδας (κνησμός 

και ξηροδερμία του τριχωτού της κεφαλής). 

2.2 Ενδείξεις

Το   σαμπουάν  Neutrogena ®   T/Gel ®   ενδείκνυται   στη   συμπτωματική 

αντιμετώπιση   της   πυτιρίδας   και   της   σμηγματορροϊκής   δερματίτιδας   του 

τριχωτού της κεφαλής.

2.3 Αντενδείξεις

Μη   χρησιμοποιείτε   το   προϊόν   σε   περίπτωση   υπερευαισθησίας   στη 

λιθανθρακόπισσα ή σε οποιοδήποτε από τα έκδοχα του  φαρμάκου.  

Να μην εφαρμόζεται σε οξείες φλεγμονές ή εκδορές του δέρματος.

Να μη χρησιμοποιείται σε παιδιά κάτω των 12 ετών.

2.4 Ιδιαίτερες προφυλάξεις και προειδοποιήσεις κατά τη χρήση

2.4.1 Γενικά

           Το σαμπουάν Neutrogena ®  T/Gel ®  προορίζεται μόνο για δερματική χρήση.

Εάν εσείς ή το παιδί σας καταπιείτε κατά λάθος το σαμπουάν  Neutrogena ® 

T/Gel ®   ζητείστε ιατρική βοήθεια 

Μη χρησιμοποιείτε το προϊόν αν είστε αλλεργικός στη λιθανθρακόπισσα ή σε 

κάποιο άλλο από τα συστατικά που αναφέρονται παραπάνω. 

Αποφύγετε την επαφή με τα μάτια. Εάν το σαμπουάν  Neutrogena ®   T/Gel ® 

έλθει σε επαφή με τα μάτια, ξεπλύνετε με άφθονο νερό. Εάν ερεθιστούν τα 

μάτια συμβουλευτείτε το φαρμακοποιό σας 

2.4.2  Κύηση ή γαλουχία

Το   σαμπουάν  Neutrogena  T/Gel  δεν   πρέπει   να   χρησιμοποιείται   κατά   την 

κύηση και τη γαλουχία, εκτός εάν οι κίνδυνοι και τα οφέλη εκτιμηθούν και 

συζητηθούν με το γιατρό σας.

2.4.3 Παιδιά

            Βλέπε 2.3 Αντενδείξεις

2.4.4 Επίδραση στην ικανότητα οδήγησης και χειρισμού μηχανημάτων

Καμία γνωστή.

2.4.3 Ιδιαίτερες προειδοποιήσεις για τα περιεχόμενα έκδοχα 

Περιέχει   παραϋδρόξυβενζοϊκά   που   μπορεί   να   προκαλέσουν   αλλεργικές 

αντιδράσεις (πιθανόν με καθυστέρηση)

2.5 Αλληλεπιδράσεις με άλλα φάρμακα ή ουσίες

Δεν υπάρχει καμία γνωστή αλληλεπίδραση του φαρμάκου με άλλα φάρμακα 

ή ουσίες.

2.6 Δοσολογία

Για δερματική χρήση μόνο.

Το  Neutrogena  T/Gel  πρέπει   να   χρησιμοποιείται   μία   ή   δύο   φορές   την 

εβδομάδα για τη θεραπεία διαταραχών του τριχωτού της κεφαλής. Η θεραπεία 

διαρκεί συνήθως 4 εβδομάδες, μετά τις οποίες πρέπει να αναμένεται εμφάνιση 

βελτίωσης.  Μεγαλύτερες  περίοδοι  θεραπείας   πρέπει   να  πραγματοποιούνται 

μόνο κάτω από την επίβλεψη γιατρού.

Οδηγίες χρήσης 

1. Βρέξτε καλά τα μαλλιά σας

2. Απλώστε άφθονη ποσότητα του σαμπουάν Neutrogena®T/Gel και κάντε 

μασάζ με τις άκρες των δακτύλων στο τριχωτό της κεφαλής

3. Αφήστε τον αφρό στο τριχωτό της κεφαλής για αρκετά λεπτά

4. Ξεπλύνετε 

5. Επαναλάβετε

6. Ξεπλύνετε πολύ καλά

2.7 Υπερδοσολογία – Αντιμετώπιση

Σε   περίπτωση   της   κατά   λάθος   κατάποσης   επικοινωνήστε   άμεσα   με   το 

Κέντρο   Δηλητηριάσεων   και   ζητήστε   άμεσα   ιατρική   συμβουλή.   Η   χρήση 

πλύσης στομάχου ή ενεργοποιημένου άνθρακα δεν συνιστάται δεδομένου ότι 

η λιθανθρακόπισσα είναι διαβρωτική. Μπορεί να χορηγηθεί υποστηρικτική 

θεραπεία.  

2.8  Τι   πρέπει   να   γνωρίζετε   σε   περίπτωση   που   παραλείψατε   να   πάρετε 

κάποια δόση

Συνεχίστε κανονικά τη θεραπεία σύμφωνα με τις οδηγίες του γιατρού.

2.9   Ανεπιθύμητες ενέργειες

Μαζί με τις επιθυμητές ενέργειες, κάθε φάρμακο μπορεί να προκαλέσει και 

ορισμένες   ανεπιθύμητες   ενέργειες,   χωρίς   πάντως   αυτό   να   σημαίνει   ότι   θα 

εμφανισθούν απαραιτήτως σε κάθε ασθενή.  Εάν εμφανισθούν, θα πρέπει να 

ενημερωθεί   ο   γιατρός   σας,   για   να   δώσει   τις   απαραίτητες   οδηγίες.   Σε 

περίπτωση   που   εμφανιστούν   ανεπιθύμητες   ενέργειες   που   δεν   αναφέρονται 

παρακάτω, ενημερώστε το γιατρό ή το φαρμακοποιό σας.

Εάν προκληθεί ερεθισμός, διακόψτε τη χρήση και συμβουλευτείτε το γιατρό ή 

το φαρμακοποιό σας.

Σε σπάνιες περιπτώσεις, μπορεί να παρατηρηθεί παροδικός αποχρωματισμός 

των ξανθών, λευκασμένων ή βαμμένων μαλλιών. 

Η   λιθανθρακόπισσα   προκαλεί   φωτοευαισθησία   και   μπορεί   να   προκαλέσει 

ερεθισμό του δέρματος και εξανθήματα παρόμοια με αυτά της ακμής. Αυτές 

οι   ανεπιθύμητες   ενέργειες   είναι   πολύ   σπάνιες   (<1/10.000).   Θα   πρέπει   να 

δίνεται προσοχή κατά την έκθεση του δέρματος στο φως του ήλιου μετά τη 

εφαρμογή του προϊόντος

Μελέτες   σε   ζώα   έδειξαν   ότι   η   χρήση   λιθανθρακόπισσας   σε   υπερβολικά 

μεγάλες ποσότητες μπορεί να σχετίζεται με την ανάπτυξη όγκων στο δέρμα 

των ζώων. Ενώ δεν έχει επιβεβαιωθεί ο κίνδυνος για ανθρώπους που έκαναν 

θεραπεία   με   λιθανθρακόπισσα,   να   μη   χρησιμοποιείται   για   μακρύ   χρονικό 

διάστημα χωρίς τη συμβουλή γιατρού

2.10  Ημερομηνία λήξης του προϊόντος

Αναγράφεται στην εσωτερική και εξωτερική συσκευασία.

Σε περίπτωση που η ημερομηνία αυτή έχει παρέλθει, μην χρησιμοποιήσετε 

το σαμπουάν.

2.11    Ιδιαίτερες προφυλάξεις για τη φύλαξη του προϊόντος

 Να μη φυλάσσεται σε θερμοκρασία μεγαλύτερη των 25 ο C.

2.12  Hμερομηνία τελευταίας αναθεώρησης του φύλλου οδηγιών

 Δεκέμβριος 2010

3.   ΠΛΗΡΟΦΟΡΙΕΣ   ΓΙΑ   ΤΗΝ   ΟΡΘΟΛΟΓΙΚΗ   ΧΡΗΣΗ   ΤΩΝ 

ΦΑΡΜΑΚΩΝ

 Το φάρμακο αυτό σας το έγραψε ο γιατρός σας μόνο για το συγκεκριμένο 

ιατρικό σας πρόβλημα.  Δεν θα πρέπει να το δίνετε σε άλλα άτομα ή να το 

χρησιμοποιείτε   για   κάποια   άλλη   πάθηση,   χωρίς   προηγουμένως   να   έχετε 

συμβουλευθεί τον γιατρό σας.

 Εάν κατά τη διάρκεια της θεραπείας εμφανισθεί κάποιο πρόβλημα με το 

φάρμακο, ενημερώστε αμέσως το γιατρό σας ή το φαρμακοποιό σας.

 Εάν   έχετε   οποιαδήποτε   ερωτηματικά   γύρω   από   τις   πληροφορίες   που 

αφορούν το φάρμακο που λαμβάνετε ή χρειάζεσθε καλύτερη ενημέρωση για 

το ιατρικό σας πρόβλημα, μη διστάσετε να ζητήσετε τις πληροφορίες αυτές 

από τον γιατρό σας ή το φαρμακοποιό σας.

 Για να είναι αποτελεσματικό και ασφαλές το φάρμακο που σας χορηγήθηκε, 

θα πρέπει να λαμβάνεται σύμφωνα με τις οδηγίες που σας δόθηκαν.

 Να μη διατηρείτε τα φάρμακα σε ερμάρια του λουτρού, διότι η ζέστη και η 

υγρασία   μπορεί   να   αλλοιώσουν   το   φάρμακο   και   να   το   καταστήσουν 

επιβλαβές για την υγεία σας.

 Να μην κρατάτε φάρμακα που δεν τα χρειάζεστε πλέον ή που έχουν ήδη 

λήξει.

 Για   μεγαλύτερη   ασφάλεια   κρατάτε   όλα   τα   φάρμακα   σε   ασφαλές   μέρος, 

μακριά από τα παιδιά.

ΤΡΟΠΟΣ ΔΙΑΘΕΣΗΣ

Δεν απαιτείται ιατρική συνταγή.

Τηλ. Κέντρου Δηλητηριάσεων : 210 7793777, Αθήνα

7-11-2018

Sprout Creek Farm Recalls "Margie" Cheese Due to Listeria Monocytogenes

Sprout Creek Farm Recalls "Margie" Cheese Due to Listeria Monocytogenes

Sprout Creek Farm of Poughkeepsie, New York is recalling 132 wheels of "Margie" cheese, because it has the potential to be contaminated with Listeria monocytogenes. Listeria monocytogenes is an organism which can cause serious and sometimes fatal infections in young children, frail or elderly people, and others with weakened immune systems.

FDA - U.S. Food and Drug Administration

2-11-2018

Barcelona Nut Company Recalls Roasted and Salted in Shell Pistachios Because of Possible Health Risk

Barcelona Nut Company Recalls Roasted and Salted in Shell Pistachios Because of Possible Health Risk

Barcelona Nut Company of Baltimore, Maryland is recalling 239 cases of roasted and salted in shell pistachios, because it has the potential to be contaminated with Salmonella, an organism that can cause serious and sometimes-fatal infections in young children, frail or elderly people, and others with weakened immune systems. Healthy persons infected with Salmonella often experience fever, diarrhea (which may be bloody), nausea, vomiting and abdominal pain.

FDA - U.S. Food and Drug Administration

30-10-2018

Food Recall of Fit & Active Southwest Veggie Stuffed Sandwiches Due to Possible Listeria monocytogenes and Salmonella Contamination in Vegetables

Food Recall of Fit & Active Southwest Veggie Stuffed Sandwiches Due to Possible Listeria monocytogenes and Salmonella Contamination in Vegetables

J&J Snack Foods Handheld Corp. of Holly Ridge, NC is voluntarily recalling two lots of Fit & Active Southwest Veggie Stuffed Sandwiches due to potential contamination with Listeria monocytogenes and Salmonella. Salmonella is an organism that can cause serious and sometimes fatal infections in young children, frail or elderly people, and others with weakened immune systems.

FDA - U.S. Food and Drug Administration

19-10-2018

Working Cow Homemade, Inc. Expands Recall of Ice Cream Products Because of Possible Health Risk

Working Cow Homemade, Inc. Expands Recall of Ice Cream Products Because of Possible Health Risk

Working Cow Homemade, Inc. of St. Petersburg, FL is expanding its voluntary recall to include all ice cream manufactured from August 29, 2017 – October 11, 2018, because it has the potential to be contaminated with Listeria monocytogenes, an organism which can cause serious and sometimes fatal infections in young children, frail or elderly people, and others with weakened immune systems. Although healthy individuals may suffer only short-term symptoms such as high fever, severe headache, stiffness, nause...

FDA - U.S. Food and Drug Administration

6-10-2018

Ladyfingers Gourmet to Go Voluntarily Recalls Signature Shaved Country Ham Rolls Due to Possible Health Risk

Ladyfingers Gourmet to Go Voluntarily Recalls Signature Shaved Country Ham Rolls Due to Possible Health Risk

Ladyfingers Caterers is voluntarily recalling its Signature Shaved Country Ham Rolls as a result of the Johnston County Hams recall. The rolls were made with ham produced by Johnston County Hams, which recently initiated a recall of its ham products due to possible contamination with Listeria monocytogenes. Listeria monocytogenes can cause serious and sometimes fatal infections in young children, frail or elderly people, and others with weakened immune systems. Although healthy individuals may suffer onl...

FDA - U.S. Food and Drug Administration

5-10-2018

Working Cow Homemade, Inc. Recalls Product Because of Possible Health Risk

Working Cow Homemade, Inc. Recalls Product Because of Possible Health Risk

Working Cow Homemade Ice Cream, Inc. of St. Petersburg, FL is conducting a voluntary recall of No Sugar Added Vanilla and No Sugar Added Chocolate ice cream manufactured in three-gallon tubs during the month of May 2018. The recall is being conducted due to a potential contamination with Listeria monocytogenes, an organism which can cause serious and sometimes fatal infections in young children, frail or elderly people, and others with weakened immune systems. Although healthy individuals may suffer only...

FDA - U.S. Food and Drug Administration

31-8-2018

Danish Medicines Agency launches new concept for National Scientific Advice

Danish Medicines Agency launches new concept for National Scientific Advice

Today, 31 August 2018, the Danish Medicines Agency is launching a new concept for National Scientific Advice for companies, hospitals and others who request advice on the requirements applicable to clinical investigation and marketing authorisations.

Danish Medicines Agency

21-8-2018

Lipari Foods Issues Voluntary Recall of Premo Brand Turkey & Cheese Wedge Sandwiches Because of Possible Health Risk

Lipari Foods Issues Voluntary Recall of Premo Brand Turkey & Cheese Wedge Sandwiches Because of Possible Health Risk

Lipari Foods, LLC has issued a voluntary recall of Premo Brand turkey and cheese wedge sandwiches produced and packaged by sister company JLM due to potential contamination of Listeria monocytogenes. Listeria monocytogenes is an organism, which can cause serious and sometimes fatal infections in young children, frail or elderly people, and others with weakened immune systems. Although healthy individuals may suffer only short-term symptoms such as high fever, severe headache, stiffness, nausea, abdominal...

FDA - U.S. Food and Drug Administration

16-8-2018

August 16, 2018: Genesee County Physician and Two Others Charged with Health Care Fraud

August 16, 2018: Genesee County Physician and Two Others Charged with Health Care Fraud

August 16, 2018: Genesee County Physician and Two Others Charged with Health Care Fraud

FDA - U.S. Food and Drug Administration

16-8-2018

Zakah Life Recalls Kratom Because Of Possible Health Risk

Zakah Life Recalls Kratom Because Of Possible Health Risk

Zakah Life, LLC of Ankeny, Iowa, is recalling the following Kratom products (Super Green Maeng Da Premium Kratom powder, Powerful Red Vein Bali Premium Kratom powder, Super Green Maeng Da Premium Kratom capsules, and Powerful Red Vein Bali Premium Kratom capsules) with expiration dates prior to 01/01/2023 because they have the potential of being contaminated with Salmonella, an organism which can cause serious and sometimes fatal infections in young children, frail or elderly people, and others with weak...

FDA - U.S. Food and Drug Administration

28-7-2018

Lipari Foods Issues Voluntary Recall of Premo Brand & Fresh Grab Turkey & Swiss Submarine Sandwiches Due to Potential Contamination of Listeria Monocytogenes

Lipari Foods Issues Voluntary Recall of Premo Brand & Fresh Grab Turkey & Swiss Submarine Sandwiches Due to Potential Contamination of Listeria Monocytogenes

Lipari Foods, LLC has issued a voluntary recall of Premo Brand and Fresh Grab turkey and Swiss submarine sandwiches produced and packaged by sister company JLM due to potential contamination of Listeria monocytogenes. Listeria monocytogenes is an organism, which can cause serious and sometimes fatal infections in young children, frail or elderly people, and others with weakened immune systems. Although healthy individuals may suffer only short-term symptoms such as high fever, severe headache, stiffness,...

FDA - U.S. Food and Drug Administration

21-6-2018

Now Health Group Inc. Recalls Select Now Real Food® Zesty Sprouting Mix Because of Possible Health Risk

Now Health Group Inc. Recalls Select Now Real Food® Zesty Sprouting Mix Because of Possible Health Risk

NOW Health Group, Inc. (NOW), of Bloomingdale, Illinois, is recalling its NOW Real Food® Zesty Sprouting Mix – Product Code 7271, Lot #3031259 and Lot #3038165 – because its primary ingredient, Crimson Clover Seeds, has the potential to be contaminated with Salmonella, an organism which can cause serious and sometimes fatal infections in young children, frail or elderly people, and others with weakened immune systems. Healthy persons infected with Salmonella often experience fever, diarrhea (which may b...

FDA - U.S. Food and Drug Administration

29-5-2018

Pious Lion Voluntary Recall Due to Possible Health Risk

Pious Lion Voluntary Recall Due to Possible Health Risk

Pious Lion located in Asheville, NC is voluntarily recalling two of their Kratom products: Pious Lion Pure Premium Potent Limited Release Pink Bali, 1 oz and Pious Lion Pure Premium Potent White Maeng DA, Bright Uplifting Energy, 4 oz due to the presence of Salmonella . Salmonella is an organism which can cause serious and sometimes fatal infections in young children, frail or elderly people, and others with weakened immune systems. Healthy persons infected with Salmonella often experience fever, diarrhe...

FDA - U.S. Food and Drug Administration

23-5-2018

Golden International Corporation  Issues Public Safety Warning For Stolen Tilapia Because  of Possible Health Risk

Golden International Corporation Issues Public Safety Warning For Stolen Tilapia Because of Possible Health Risk

Golden International Corporation of Renton, WA is issuing a public safety notice for 405 cartons of stolen frozen tilapia, because it has the potential to be contaminated with Salmonella, an organism which can cause serious and sometimes fatal infections in young children, frail or elderly people, and others with weakened immune systems. Healthy persons infected with Salmonella often experience fever, diarrhea (which may be bloody), nausea, vomiting and abdominal pain. In rare circumstances, infection wi...

FDA - U.S. Food and Drug Administration

21-5-2018

Ziyad Brothers Importing Recalls Tahini Because of Possible Health Risk

Ziyad Brothers Importing Recalls Tahini Because of Possible Health Risk

Ziyad Brothers Importing is voluntarily recalling certain lot codes of Ziyad Brand Tahini because it has the potential to be contaminated with Salmonella, an organism which can cause serious and sometimes fatal infections in young children, frail or elderly people, and others with weakened immune systems. Healthy persons infected with Salmonella often experience fever, diarrhea, nausea, vomiting, and abdominal pain. In rare circumstances, infection with Salmonella can result in the organism getting into ...

FDA - U.S. Food and Drug Administration

19-5-2018

Hickory Harvest Recalls Certain Island Fruit Mix and Organic Nut Mix Products Because of Possible Health Risk

Hickory Harvest Recalls Certain Island Fruit Mix and Organic Nut Mix Products Because of Possible Health Risk

Hickory Harvest Foods of Akron, Ohio is voluntarily recalling specific lots due to the potential exposure to Listeria monocytogenes. Listeria monocytogenes, an organism which can cause serious and sometimes fatal infections in young children, frail or elderly people, pregnant women, and others with weakened immune systems. Healthy individuals may experience short-term symptoms such as high fever, severe headache, stiffness, nausea, abdominal pain, and diarrhea. Listeria infection can also cause miscarr...

FDA - U.S. Food and Drug Administration

8-5-2018

What to Know When Buying or Using a Breast Pump

What to Know When Buying or Using a Breast Pump

Breast pumps are medical devices regulated by the U.S. Food and Drug Administration. They can be used to extract milk, maintain or increase a woman's milk supply, and relieve engorged breasts (among other indications). But, to protect mothers and their babies, there are important safety considerations to know before using one.

FDA - U.S. Food and Drug Administration

4-5-2018

Maya Distribution, LLC Recalls Dragon Label Kratom Because Of Possible Salmonella Contamination

Maya Distribution, LLC Recalls Dragon Label Kratom Because Of Possible Salmonella Contamination

Maya Distribution, LLC of South Salt Lake City, Utah is voluntarily recalling Dragon Kratom labeled bottles and sealed packages of encapsulated and raw powder product because it has the potential to be contaminated with Salmonella, an organism which can cause serious and sometimes fatal infections in young children, frail or elderly people, and others with weakened immune systems. 

FDA - U.S. Food and Drug Administration

19-4-2018

Certain Kratom-Containing Powder Products by Viable Solutions: Recall -Possible Salmonella Contamination

Certain Kratom-Containing Powder Products by Viable Solutions: Recall -Possible Salmonella Contamination

Viable Solutions of Nampa, ID has initiated a recall of certain Kratom-containing powder products, because it has the potential to be contaminated with Salmonella, an organism which can cause serious and sometimes fatal infections in young children, frail or elderly people, and others with weakened immune systems. Healthy persons infected with Salmonella often experience fever, diarrhea (which may be bloody), nausea, vomiting and abdominal pain. In rare circumstances, infection with Salmonella can result...

FDA - U.S. Food and Drug Administration

19-4-2018

NxtGen Botanicals Maeng Da Kratom by NGB Corp.: Recall - Possible Salmonella Contamination

NxtGen Botanicals Maeng Da Kratom by NGB Corp.: Recall - Possible Salmonella Contamination

NGB Corp. of West Jordan, Utah is voluntarily recalling NxtGen Botanicals Maeng Da Kratom labeled bottles of encapsulated product because it has the potential to be contaminated with Salmonella, an organism which can cause serious and sometimes fatal infections in young children, frail or elderly people, and others with weakened immune systems. Healthy persons infected with Salmonella often experience fever, diarrhea (which may be bloody), nausea, vomiting and abdominal pain. In rare circumstances, infec...

FDA - U.S. Food and Drug Administration

22-3-2018

New concept for national scientific advice

New concept for national scientific advice

The Danish Medicines Agency will soon launch a new national scientific advice concept for companies, hospital researchers and others who require advice on requirements for marketing authorisations or clinical trials.

Danish Medicines Agency

27-2-2014

Paracetamol use during pregnancy

Paracetamol use during pregnancy

A new Danish study suggests a possible connection between mothers' use of paracetamol painkillers during pregnancy and the risk of developing disorders like ADHD (attention deficit hyperactivity disorder) in children.

Danish Medicines Agency

24-7-2013

Danish Pharmacovigilance Update, 27 June 2013

Danish Pharmacovigilance Update, 27 June 2013

In this issue of Danish Pharmacovigilance Update: The benefits of medicines for the treatment of acne (Diane® Mite and others) continue to outweigh the risks of use within the indication.

Danish Medicines Agency

6-9-2012

Danish Pharmacovigilance Update, 16 August 2012

Danish Pharmacovigilance Update, 16 August 2012

Among the topics covered in this issue of Danish Pharmacovigilance Update are: Maximum single dose of intravenous ondansetron (Zofran® and others) now restricted to 16 mg.

Danish Medicines Agency

3-1-2012

Danish Pharmacovigilance Update, 15 December 2011

Danish Pharmacovigilance Update, 15 December 2011

Among the topics covered in this issue of Danish Pharmacovigilance Update are: Atomoxetine (Strattera®) and the risk of increased blood pressure and heart rate, increased suspicion of risk of congenital malformations with the antiepileptic topiramate (Topimax® and others), and new recommendations for the antidepressant escitalopram.

Danish Medicines Agency

11-9-2018

We will always remember those who have fallen and the heroes who risked their lives to treat and save others. #September11, #NeverForgetpic.twitter.com/LJrMEBE2SU

We will always remember those who have fallen and the heroes who risked their lives to treat and save others. #September11, #NeverForgetpic.twitter.com/LJrMEBE2SU

We will always remember those who have fallen and the heroes who risked their lives to treat and save others. #September11, #NeverForget pic.twitter.com/LJrMEBE2SU

FDA - U.S. Food and Drug Administration

1-6-2018

hydrocodone (Vicodin®), codeine, morphine, and many others. #DYK #FDAInnovationChallenge (2 of 2 messages)  https://go.usa.gov/xQwmW pic.twitter.com/bGlnTFOzVE

hydrocodone (Vicodin®), codeine, morphine, and many others. #DYK #FDAInnovationChallenge (2 of 2 messages) https://go.usa.gov/xQwmW pic.twitter.com/bGlnTFOzVE

hydrocodone (Vicodin®), codeine, morphine, and many others. #DYK #FDAInnovationChallenge (2 of 2 messages) https://go.usa.gov/xQwmW  pic.twitter.com/bGlnTFOzVE

FDA - U.S. Food and Drug Administration