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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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You can also report adverse reactions or quality problems to the FDA's MedWatch Adverse Event Reporting program either online, by regular mail, or by fax at 800-FDA-0178. And for more information on this drug, you can visit the agency's website. RELATED: This Product Sold by Amazon Fresh Was Just Recalled, FDA Warns.
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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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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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If you need to report an adverse event/side effect or a product quality complaint for a US GSK Consumer Healthcare product, please call us at 1-800-245-1040, Monday through Friday, 8 AM to 6 PM EST (excluding major holidays), or email us by clicking the button below or sending an email to [email protected]. Report adverse event.
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pharmacovigilance.czech@bayer.com 24/7 emergency hotline: +420 731 620 359 fax: +420 266 101 504. If you wish to report an adverse event related to a Bayer product, please fill out an adverse event report and send it to the State Institute for Drug Control or to Bayer on the above mentioned contacts.
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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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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.
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.
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.
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.
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).