Adverse Action Phone Number

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+1-862-263-0820

US Headquarters. Advanced Accelerator Applications USA, Inc. 57 E. Willow Street. Millburn, NJ 07041 USA. Tel: +1-862-263-0820. Fax: +1-862-263-0840. General Inquiries or Media Contacts, click here. Adverse Event Reporting: If you would like to report an adverse drug reaction related to the use of one of our products, click here.

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Updated: 2 hours ago

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373821785385

Marvel Legends Black Widow Comic Book Heroes Plastic Action Figures, Black Widow Marvel Action Action Figures, Black Widow Marvel Action Figures & Accessories, Marvel Legends Hawkeye Comic Book Heroes Action Figures, Black Widow Marvel Universe Action Accessories, Black Widow Marvel Universe Action Figure Accessories,

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Updated: 3 hours ago

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519-937-1522

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Updated: 8 hours ago

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800-822-7967

To report SUSPECTED ADVERSE REACTIONS, contact MassBiologics at 1-800-457-4626 or Vaccine Adverse Event Reporting System (VAERS) at 1-800-822-7967 or www.vaers.hhs.gov. Please see full Prescribing Information for Tetanus Diphtheria Toxoi

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Updated: just now

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866-663-3762

To Report an Adverse Event or Product Complaint: Call: 1-866-MODERNA (1-866-663-3762) 24 hours, 7 days a week. Or fax adverse events to: 1-617-649-3910

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Updated: 1 hours ago

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888-474-3657

Grifols USA was established in 2003. Based in Los Angeles, we cover the U.S. market where we offer a comprehensive portfolio of products and services from the Bioscience, Diagnostic, Hospital, and Bio Supplies divisions. The company is one of the largest producers of lifesaving plasma medicines in the world due to strategic investments in the U ...

  • Legal basis: Consent
  • Recipients: Grifols group companies

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Updated: 4 hours ago

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888.204.7616

Follow the process on the website at You can call Medtronic at 1.888.204.7616. You can also report an adverse event to the FDA’s MedWatch Adverse Event Reporting program: Report by telephone: 1.800.FDA.1088 Fax report: 1.800.FDA.0178 Con

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Updated: 4 hours ago

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  • Frequently Asked Questions

  • Where can i find information on adverse reactions to products in canada?

    Contact the Canada Vigilance Program for information on adverse reactions to the following health products marketed in Canada: pharmaceuticals, biologics (including fractionated blood products as well as therapeutic and diagnostic vaccines), natural health products and radiopharmaceuticals.

  • How do i contact wala about adverse drug reactions?

    If you have any questions please call us under +49 7164 930-181. If you would like to report a suspected adverse drug reaction (side-effect) in relation to a WALA medicine, please contact us here. The fields marked with * must be completed.

  • What are the possible adverse reactions to M-M-R®II?

    The following adverse reactions have been identified during clinical trials or reported during post-approval use of M-M-R®II or its components: fever, headache, dizziness, rash, injection-site reactions, febrile convulsions, anaphylaxis and anaphylactoid reactions, arthritis, thrombocytopenia, encephalitis and encephalopathy.

  • What are the possible adverse reactions to tukysa?

    Serious adverse reactions occurred in 26% of patients who received TUKYSA; those occurring in ≥2% of patients were diarrhea (4%), vomiting (2.5%), nausea (2%), abdominal pain (2%), and seizure (2%). Fatal adverse reactions occurred in 2% of patients who received TUKYSA including sudden death, sepsis, dehydration, and cardiogenic shock.

  • How do I report a possible adverse event associated with Zoetis?

    To report a possible adverse event associated with a Zoetis product, including human exposure, contact the Veterinary Medical Information Support Team in your region using the drop down menu below. In the U.S., call 1-888-Zoetis1 (1-888-963-8471).

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