Adverse Event Report

To report an Adverse Event for a Paratek product, please complete this form or call us 1-833-PARATEK (1-833-727-2835).

Reporter Name and Contact Information

First Name*

Last Name*

Specialty

Title*

Address Line 1*

Address Line 2

State/Province*

Postal Code*

Country*

Email*

Phone*

Adverse Event Report

Name of Suspect Paratek Product*

Select Other Product, if you don't see the medication you are looking for in the list.

Patient Identifier (provide at least one of the following):
*

Patient Initials

Patient Age or Year of Birth

Patient Sex (M/F)

Indication*

Dosing/Route/Action Taken with Paratek Product:*

Details of Suspected Adverse Reaction: (Onset, Treatment, Relevant Test Results)*

Concomitant Medication(s)*

If the patient is the reporter, may we contact their Healthcare provider?*

Outcome of the Event*

Your submission has been received!

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Contact Us

If you would like to speak to a Paratek Medical Information Professional please call 1-833-PARATEK (1-833-727-2835) or email medinfo@paratekpharma.com. Otherwise please see below.

Medical Information

If you would like to speak to a Paratek Medical Information Professional or speak with a Field Medical professional about NUZYRA®:
‍
Call: 1-833-PARATEK (1-833-727-2835)
Email: medinfo@paratekpharma.com

With our commitment to patient safety, if you are reporting an adverse event or product complaint, please report as much relevant information as possible which may include product indication, lot number and return availability.

If you would like to speak to a Paratek Medical Information Professional or speak with a Field Medical professional about XHANCE®:

Call: 1-833-678-6673
Email: ReportAE@optinose.com

Report a Product Complaint

To report a Product Quality Complaint for NUZYRA®:

Call: 1-833-PARATEK (1-833-727-2835)
Email: drugsafety@propharmagroup.com

To report a Product Quality Complaint for XHANCE®:
Call: 1-833-678-6673
Email: ReportAE@optinose.com

Report an Adverse Event

To report an Adverse Event for NUZYRA®:

Call: 1-833-PARATEK (1-833-727-2835)
Email: drugsafety@propharmagroup.com

To report an Adverse Event for XHANCE®:
Call:  1-833-678-6673
Email:  ReportAE@optinose.com

You can also contact the FDA:

Call:  1-800-FDA-1088
Email: www.fda.gov/medwatch

Welcome to Paratek
Medical Affairs

Welcome to Paratek
Medical Affairs

Welcome to Paratek
Medical Affairs

Adverse Event Report

To report an Adverse Event for a Paratek product, please complete this form or call us 1-833-PARATEK (1-833-727-2835).

Reporter Name and Contact Information

Adverse Event Report

Contact Us

If you would like to speak to a Paratek Medical Information Professional please call 1-833-PARATEK (1-833-727-2835) or email medinfo@paratekpharma.com. Otherwise please see below.

Medical Information

Report a Product Complaint

Report an Adverse Event

King of Prussia

Boston

Welcome to ParatekMedical Affairs

Welcome to ParatekMedical Affairs

Welcome to ParatekMedical Affairs

Adverse Event Report

To report an Adverse Event for a Paratek product, please complete this form or call us 1-833-PARATEK (1-833-727-2835).

Reporter Name and Contact Information

Adverse Event Report

Contact Us

If you would like to speak to a Paratek Medical Information Professional please call 1-833-PARATEK (1-833-727-2835) or email medinfo@paratekpharma.com. Otherwise please see below.

Medical Information

Report a Product Complaint

Report an Adverse Event

King of Prussia

Boston

Welcome to Paratek
Medical Affairs

Welcome to Paratek
Medical Affairs

Welcome to Paratek
Medical Affairs