The Header Sliders are Full-Width

With the live area occupying 50% of the screen size.

The slider has a relative height:

It is always as tall as the slide with the longest copy.

So if a slide has a lot of copy, the whole slider will be taller and the image width will crop accordingly to accommodate the container’s size.

This is a Ttitle

This is a Subtitle.

With a Paragraph description.

And some small text too (H6).

The button goes at the end

Choosing the consistent dimensions for the image sizes will ensure they look good on all screen-sizes!

Exporting the images at the right resolutions will ensure that the websites are light-weight and fast to load every time.

This is a Full Width Image

It takes the full width of the screen. It should be a horizontal image. It has a zoom-in parallax effect to it.

It has a relative height to how much content there is in the container.

800-1200px wide
150dpi
Up to 850KB

This is a Large Image

It takes a full column of content and it is centered.

800-1200px wide • 150dpi • Up to 750KB

This is a Medium Image

It takes half the screen size in width.

Their default height is to be relative to the copy height. So they will be as tall as the copy.

This can be overwritten in specific cases where the image needs to maintain it’s full height.

500-800px wide
150dpi
Up to 250KB

This is a Medium Graphic

It takes half the screen size in width and it will be top-aligned with the copy.

500-800px wide
150dpi
Up to 250KB

Small Images

These images are organized in rows of three.

INDICATIONS AND USAGE | IMPORTANT SAFETY INFORMATION

PRODUCT NAME®

IMPORTANT SAFETY INFORMATION
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INDICATIONS AND USAGE | IMPORTANT SAFETY INFORMATION

PRODUCT NAME®

IMPORTANT SAFETY INFORMATION
WARNING: Lorem ipsum dolor sit amet, consectetur adipiscing elit.

in echocardiography to opacify the left ventricular chamber and to improve the delineation of the left ventricular endocardial border in adult and pediatric patients with suboptimal echocardiograms
in ultrasonography of the liver for characterization of focal liver lesions in adult and pediatric patients
in ultrasonography of the urinary tract for the evaluation of suspected or known vesicoureteral reflux in pediatric patients

IMPORTANT SAFETY INFORMATION

WARNING: SERIOUS CARDIOPULMONARY REACTIONS

Serious cardiopulmonary reactions, including fatalities, have occurred uncommonly during or following the injection of ultrasound contrast agents, including sulfur hexafluoride lipid microspheres. Most serious reactions occur within 30 minutes of administration.

Assess all patients for the presence of any condition that precludes administration
Always have resuscitation equipment and trained personnel readily available

Contraindications

LUMASON (sulfur hexafluoride lipid-type A microspheres) for injectable suspension, for intravenous use or intravesical use is contraindicated in patients with known or suspected hypersensitivity to sulfur hexafluoride lipid microsphere or its components, such as polyethylene glycol (PEG).

Warnings

Serious cardiopulmonary reactions, including fatalities, have occurred uncommonly during or shortly following administration of ultrasound contrast agents, including LUMASON. Always have cardiopulmonary resuscitation personnel and equipment readily available prior to LUMASON administration and monitor all patients for acute reactions.

Post-marketing hypersensitivity reactions, including serious hypersensitivity reactions, have been observed during use or shortly following LUMASON administration. These reactions may occur in patients with no history of prior exposure to sulfur hexafluoride lipid-containing microspheres. LUMASON contains PEG. There may be increased risk of serious reactions including death in patients with prior hypersensitivity reaction(s) to PEG.

Systemic embolization may occur in patients with cardiac shunts. Assess patients with cardiac shunts for embolic phenomena following LUMASON administration.

There is a risk of ventricular arrhythmia related to high mechanical index in patients administered LUMASON. LUMASON is not recommended for use at mechanical indices greater than 0.8.

The most common adverse reactions (incidence ≥ 0.5%) are headache (1%) and nausea (0.5%).

You are encouraged to report negative side effects of prescription drugs to the FDA. Visit www.fda.gov/medwatch or call 1-800-FDA-1088.

Please click here for full Prescribing Information for LUMASON ultrasound contrast agent, including BOXED WARNING on Serious Cardiopulmonary Reactions.

LUMASON is manufactured for Bracco Diagnostics Inc., Monroe Township, NJ 08831 by Bracco Suisse S.A., Plan-les-Ouates Geneve, Switzerland (LUMASON lyophilized powder vial-25 mg lipid-type A/60.7 sulfur hexafluoride gas); Vetter Pharma-Fertigung GmbH & Co. KG, 88212 Ravensburg, Germany (Sodium Chloride 0.9% Injection, USP); B. Braun Melsungen AG, 34212 Melsungen, Germany (Mini-Spike).

LUMASON and SONOVUE are registered trademarks of Bracco Diagnostics Inc. and its affiliated entities.

All other trademarks and registered trademarks are the property of their respective owners.

IMPORTANT SAFETY INFORMATION | ISOVUE® (Iopamidol Injection) solution

PRODUCT NAME®

IMPORTANT SAFETY INFORMATION
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