Augment bundle

The augment's value.Augments take an extremely long time to max; expect to spend at least hundreds of Last Laugh tickets to max Health and Damage on a single character. While Crit Chance and Damage augments seem to be rarer, it takes less of them to max so overall it is slightly easier to max those. It may take months of pure game time to fully augment all characters. Regardless, this is the amount of how many cards are need to fully max out a character:Health/Damage: 38 Major, or 75 Medium or 150 Minor Augment CardsCrit Chance: 10 Major, or 17 Medium or 50 Minor Augment CardsCrit Damage: 13 Major, or 25 Medium or 50 Minor Augment CardsAmounts of Augment per cardXPMajor Augment: +10,000 XPMedium Augment: +5,000 XPMinor Augment: +2,500 XPDamageMajor Augment: +8 base damageMedium Augment: +4 base damageMinor Augment: +2 base damageHealthMajor Augment: +8 base healthMedium Augment: +4 base healthMinor Augment: +2 base healthCrit DamageMajor Augment: +8% base crit damageMedium Augment: +4% base crit damageMinor Augment: +2% base crit damageCrit ChanceMajor Augment: +5% base crit chanceMedium Augment: +3% base crit chanceMinor Augment: +1% base crit chanceComparisonBelow is the comparison stats gained from maxed damage and health augments (+300 to base each) between each card rarity (at highest level and promotion). Gold characters prove to be the most effective users of damage and health augments due to their high stats increases from promotion.AugmentBronzeSilverGoldMetalMax damage bonus from augment5,6709,45012,2856,211.8Max health bonus from augment11,52019,20024,96011,566.8Online BattleHealth and damage augments do not take effect on characters on the Defense's team in Online Battle. This applies to characters on teams found in matchmaker and teams you challenge in revenge, and also applies to your team when it is found or challenged. However, characters will still have modified base crit chance and crit damage if they are so

*As of September, 2024**A majority of patients studied in the two pivotal studies evaluating Augment Injectable also presented with one or more risk factors for non-union. We polled orthopaedic surgeons on which biologics brand they prefer for hindfoot and ankle fusions.One choice stood out.Augment Regenerative solutionsWhen choosing a biologic for hindfoot and ankle arthrodesis, preference matters, and you’ve told us yours. Considered by many to be a standard of care for hindfoot and ankle arthrodesis1, Augment provides predictable outcomes to guarantee your peace of mind. You deserve performance and peace of mind.Augment delivers both.Augment is the safe, efficacious and only level 1 clinically demonstrated option for hindfoot and ankle arthrodesis, as evidenced in the largest randomized controlled trial (RCT) conducted in foot and ankle orthopaedic history. Augment is backed by Stryker’s Augment Satisfaction Guarantee.*** ***Stryker’s Augment Satisfaction Guarantee provides a replacement Augment kit to a facility if a patient develops a nonunion at one or more of the ankle or hindfoot joints where Augment was implanted. The facility must meet the terms and conditions of the guarantee for the replacement to be provided. WarningsAs with all therapeutic recombinant proteins, there is a potential for immune responses to be generated to the rhPDGF-BB component of Augment Bone Graft and Augment Injectable. The immune response to rhPDGF-BB was evaluated for Augment Injectable in two studies, and for Augment Bone Graft (which contains the identical rhPDGF-BB) in two pilot and one pivotal study for ankle and hindfoot arthrodesis procedures. The detection of antibody formation is highly dependent on the sensitivity and specificity of the assay. Additionally, the observed incidence of antibody (including neutralizing antibody) positivity in an assay may be influenced by several factors including assay methodology, sample handling, timing of sample collection, concomitant medications, and underlying disease. For these reasons, comparison of the incidence of antibodies to Augment Bone Graft or Augment Injectable with the incidence of antibodies to other products may be misleading.Women of childbearing potential should avoid becoming pregnant for one year following treatment with Augment Bone Graft or Augment Injectable. The implantation of rhPDGF-BB in women and the influence of their development of anti-PDGF-BB antibodies, with or without neutralizing activity, on human fetal development are not known.The safety and effectiveness of Augment Bone Graft or Augment Injectable in nursing mothers has not been established. It is not known if rhPDGF-BB is excreted in human milk.The safety and effectiveness of

Augment Bone Graft or Augment Injectable has not been established in anatomical locations other than the ankle or hindfoot, or when combined with autologous bone or other bone grafting materials.The safety and effectiveness of repeat applications of Augment Bone Graft or Augment Injectable have not been established. The safety and effectiveness of Augment Bone Graft or Augment Injectable in pediatric patients below the age of 18 years have not been established.Augment Bone Graft or Augment Injectable do not have any biomechanical strength and must be used in conjunction with standard orthopedic hardware to achieve rigid fixation. The β-TCP component is radiopaque, which must be considered when evaluating radiographs for the assessment of bridging bone. The radiopacity may also mask underlying pathological conditions. Over time, the β-TCP is intended to be resorbed at the fusion site and replaced by new bone. Under such circumstances, it would typically be indistinguishable from surrounding bone.

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