Filter Type: All Time (7 Results) Past 24 Hours Past Week Past month Post Your Comments?
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.
Preview / Show more
Updated: 2 hours ago
See Also:Number System And Its Applications, Advanced Tech Support Contact Us, Verify It Show details
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,
Preview / Show more
Updated: 3 hours ago
See Also:Marvel Black Widow Phone Number, Exclusive Phone Number, Verify It Show details
Kelbly Atlas Tactical Action, Long Action, 308 Bolt Face, RB-RP, Flat Bolt Head $1,399.99 In Stock Brand: Kelbly Item Number: # KELBLY ATLAS TACTICAL ACTION LA 308 Kelbly Atlas Tactical Action, Short Action, RB-RP, MAG Bolt Face, Flat Bolt Head $1,399.99 In Stock Brand: Kelbly Item Number: # KELBLY ATLAS TAC S/A MAG MRA Maverick Rifle, 308 Win, 20" Barrel $1,799.95 In …
Preview / Show more
Updated: 8 hours ago
See Also:Buy Phone Number Online For Sms, Tikka Rifles Phone Number, Verify It Show details
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
Preview / Show more
Updated: just now
See Also:Td Mortgage Center Contact, Td First Class Travel Visa Contact, Verify It Show details
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
Preview / Show more
Updated: 1 hours ago
See Also:Teton Science School Contact, New Contact Lenses Technology , Verify It Show details
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 ...
Preview / Show more
Updated: 4 hours ago
See Also:Grifols Phone Number, Grifols Provo Phone Number, Verify It Show details
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
Preview / Show more
Updated: 4 hours ago
See Also:Carelink Medtronic Phone Number, Diabetes Freedom Phone Number, Verify It Show details
All Time (7 Results)
Past 24 Hours
Past Week
Past month
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).