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Op Ed # 633 European Medical Agency Reveals Millions of Deaths And 4.9 Million Injuries From “modmRNA” COVID-19 Injections, Now The Same “modmRNA” is in Flu Shots

  • Op Ed # 633 European Medical Agency Reveals Millions of Deaths And 4.9 Million Injuries From “modmRNA” COVID-19 Injections, Now The Same “modmRNA” is in Flu Shots

By Capt Joseph R. John, September 20, 2023

Based upon the below listed article quoting scientists about the experimental test gene therapy COVID-19 injections advertised as using mRNA (they should never have been called vaccines according to the 100-year-old medical definition of a vaccine).  The world population were misled, harmed, injured, and killed by pharmaceutical companies, who made fortunes from the experimental test gene therapy COVID-19 inoculations advertised as using mRNA.  The mRNA does not last in the body long enough for the inoculations to be effective.  The pharmaceutical companies that created the experimental test gene therapy COVID-19 inoculations, therefore used the manufactured substance, "modmRNA".  That misinformation, which is a lie by omission, enabled use of a substance that harmed, injured, crippled, and killed far too many people as explained by European Medical Agency (EMA) in the below listed article. 

As reported in the below listed confidential document from the EU, released by BioNTech to the EU’s European Medical Agency (EMA), it was revealed that 4,964,106 adverse side events were reported by people who received the experimental test gene therapy Pfizer and BioNTech “modmRNA” COVID-19 injection.  The EMA further reported that millions of deaths occurred among people who received the experimental test gene therapy Pfizer and BioNTech “modmRNA” COVID-19, at a time when the pharmaceutical companies that created the experimental test gene therapy injections were insisting that they saw no “safety signals.”

The EMA, honestly reported millions of deaths and 4,964,106 adverse side events occurred from the injection of the experimental test gene therapy Pfizer and BioNTech “modmRNA” COVID-19.  The NIH and CDC under the control of Dr. Anthony Fauci tried to cover up the fact that over one million Americans died from the experimental test gene therapy Pfizer “modmRNA” COVID-19 injections, and 6.5 million Americans had adverse side events, that were reported to the Vaccine Adverse Events Reporting System (VAERS) as a result of the experimental test gene therapy Pfizer and BioNTech “modmRNA” COVID-19 injections. 

Despite those alarming clinical findings, reported to the CDC by VAERS, the CDC made a decision that in the future, the collection of any new adverse side events, and reporting them to the VAERS is somehow no longer of interest to the medical community or the America’s Public Health System.  The 6.5 million VAERS adverse side events was eliminated from the CDC website.  That was a political decision by the Biden/Obama administration to cover up the danger the COVID-19 inoculations created, in preparation to force the COVID-19 inoculation into all Americans, prior to the 2024 election. 

Existing data from the last COVID-19 injections reported to VAERS showed around 6.5 million adverse events/health impacts out of 10.1 million users, with around 2 million of those people being, so severely injured that they are now unable to conduct normal activities of daily living and now need medical care, according to a third-party rendering of its findings.  In other words, despite “modmRNA” shots still being widely available and the CDC is aggressively promoting its future use.  The “case is closed” with regards to collecting new VAERS safety reports under today’s Federal Public Health Administration, and preventing the analysis of future major injuries and disabilities.

Pfizer knew that they were killing babies in utero and knew they were making nursing newborns, born to moms who were injected with the COVID-19 experimental test gene therapy, severely ill.  Yet Pfizer promoted the “modmRNA” injections for pregnant women (that resulted in thousands of miscarriages that were reported by pregnant women who were inoculated).  Dr. James Thorp, a well-known medical practitioner, whose practice is with pregnant women and babies has been one of the very few medical providers that raised the alarm about the massive loss of babies from the miscarriages of women who were injected with the COVID-19 experimental test gene therapy and making nursing newborns, born to those injected women severely ill, that the Pfizer “modmRNA” injection created.

President Trump protected the pharmaceutical companies, that created the experimental test gene therapy COVID-19 injections, from potential lawsuits of Americans severely injured and disabled by adverse side events from the inoculation.  President Trump did what he believed would help speed up the creation of a vaccine to rapidly protect Americans from death, if infected by the Wuhan Virus.  However, President Trump was lied to by Dr Anthony Fauci and other scheming, money-hungry and power-hungry scientists, pharmaceutical companies, investors, and others who told the leftist liberal media establishment and all Americans that the experimental test gene therapy inoculations were safe, but those experimental test gene therapy injections were never approved by the FDA as being safe for human use, and they still have not been approved by the FDA as being safe for human use, except for “emergency” use only. 

Dr. Anthony Fauci was criminally referred by Senator Rand Paul (R-Ky.) to the Department of Justice for lying during Congressional testimony in 2021, when he said he did not fund the gain-of-function research that created the Wuhan Virus at the Wuhan Institute of Virology (WIV) in Communist China.  Fauci insisted repeatedly in Congressional testimony that the National Institutes of Health (NIH), that he ran, had never funded gain-of-function research which created the Wuhan Virus at the WIV.  Sen Paul proved that Fauci was lying to Congress during his false testimony, and that the research he funded was done on viruses at WIV, was, in fact, gain-of-function research, and matched the NIH’s own description of gain-of-function research. 

Fauci had previously been ordered by the Obama administration to cease funding gain-of-function research because it was “extremely dangerous”; Fauci disobeyed those orders and continued to support and fund the gain-of-function research in Communist China, behind the back of the Obama administration, and created the Wuhan Virus (Covid-19) that injured and crippled over 6.5 million Americans and killed over one million Americans.

"Throughout Pfizer's pandemic dominance, the company has been partnering with BioNTech on “modmRNA” research and a global manufacturing expansion. Their success with COVID-19 gene therapy experimental test inoculations allowed the German “modmRNA” specialist to catapult to the No. 2 spot.  Coming in third, is the Communist Chinese experimental gene therapy inoculation, Sinovac, which reportedly obtained more than $19 billion in sales last year. 

Moderna, which did not market any products at the time of the last vaccine rankings, jumped over its larger Big Pharma rivals to rank in fourth place by revenues this year.  The company’s Spikevax drove a massive revenue increase from 2020 to 2021, a time when Moderna had been busy scaling its global presence to support future growth."

WARNING:  Both Pfizer and Moderna are talking about using the same technology, "modmRNA" that they used in their COVID-19 gene therapy experimental test inoculation, now is in their “flu shots”; Americans should reject flu shots from Pfizer and Moderna who are using “modmRNA” in their flu shots and get flu shots from pharmaceutical companies not using “modmRNA”. 

The left-leaning intellectuals, the liberal elite, the leftist propaganda media establishment, the pharmaceutical companies, Bill Gates, the Socialist Democrats, and the Biden/Obama administration are preparing to try to force every American, including infants and pregnant women, to be injected by the “new” and dangerous COVID-19 variant (that has not been tested for two years to prove it is safe for injection in humans).  Their goal is to catapult the nation into a full-fledged pandemic they are preparing to declare, that they say is coming, prior to the 2024 election, so they can prevent voters from going to the polls to vote. 

A CNN host recently made the comment, that it “may be time to break out the masks”.  Aerosolized viruses — especially COVID-19, is about half the size of influenza viruses; that very small aerosol cannot be blocked by a porous mask.  Masks have a weave that leaves space between the threads that is 10 times the size of the COVID-19 virus; when the wearer breaths, the virus can freely pass in and out of the mask.  Masks are treated with formaldehyde to stop mold growth, so the wearer is breathing in some formaldehyde which can cause cancer.  As the moisture from one’s breath dampens the mask, the mask picks up bacteria, which grows rapidly, so the wearers of the mask breaths in a hoist of bad bacteria.  Masks don’t work at all as proven in this large Bangladesh study; not a single randomized study has shown that there is no protective effect that is statistically significant at all.    

The Biden/Obama administration has already funded $1.4 billion for a “new” experimental test COVID-19 gene therapy inoculation “For All Americans”, whether they had previously been injected the experimental test COVID-19 gene therapy inoculation in the past.

“BUYERS BEWARE!!”  Before taking a flu shot, call and ask who manufactured the shot and research if the pharmaceutical company used the same "modmRNA" that they used to manufacture their gene therapy COVID-19 experimental test inoculation and has the “modmRNA” in their flu shot.  Americans should not risk their health, their lives, or the health of their loved ones to enrich the greedy pharmaceutical companies using “modmRNA” when they now know it was misrepresented and it would be extremely dangerous as explained below. 

If Pfizer or Moderna manufactured the flu shot you are considering to be injected with, refuse to take it from those harmful pharmaceutical companies.  The “modmRNA” injections inhibits human immunity and suppression of cancer (please click on the follow on and below listed link).  It was found that “modmRNA” damages the heart, the brain, and causes blood clots.  They also interfere with two tumor suppressor systems, the p53 tumor suppressor protein and BRCA, or the Breast Cancer gene.  Those RNA shots are causing the surge in cancer cases across the world and can be fully documented by clicking on the below link.

Unlike the European Medical Agency (EMA), that warned Europeans of the dangers of the COVID-19 experimental test gene therapy inoculation, outlined in the below listed document, the NIH and CDC continue to lie to the American people about how the COVID-19 experimental test gene therapy inoculation injured and crippled 6.5 million Americans with adverse side events as reported to VAERS (the CDC even removed that information from their Website), and they attempted to cover up the deaths of over one million Americans from the COVID-19 inoculations.  The EU openly revealed that millions of deaths resulted from the COVID-19 experimental test gene therapy inoculations, that also injured and crippled 4,964,106 Europeans in adverse side events from the Pfizer and BioNTech “modmRNA” COVID-19 inoculations.

Copyright by Capt Joseph R. John.  All Rights Reserved.  The material can only be posted on another Website or distributed on the Internet by giving full credit to the author.  It may be published, broadcast, or rewritten without the permission from the author.




“Criminal”: Confidential EU Documents Reveal Thousands of Deaths From Pfizer-BioNTech Shots

“Confidential” documents released by BioNTech to the European Medicines Agency reveal tens of thousands of serious adverse events and thousands of deaths among people who received the Pfizer-BioNTech mRNA COVID-19 vaccine during a time period when the vaccine makers insisted they saw no “safety signals.”

By Michael Nevradakis, Ph.D.  6/23/23

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Documents released by BioNTech to the European Medicines Agency (EMA) reveal tens of thousands of serious adverse events and thousands of deaths among people who received the Pfizer-BioNTech mRNA COVID-19 experimental injection.

The documents, dated Aug. 18, 2022, and marked “confidential,” show that cumulatively, during the clinical trials and post-marketing period up to June 18, 2022, a total of 4,964,106 adverse events were recorded. The documents included an appendix with further details about the specifics about the identified adverse events.

Among children under age 17, 189 deaths and thousands of serious adverse events were reported.

The documents present data collected between Dec. 19, 2021, and June 18, 2022 (the “PSUR #3 period”), in addition to cumulative data on adverse events and deaths that occurred among those who received the vaccine during clinical trials and during the post-marketing period, beginning December 2020 up until June 18, 2022.

During this time, Pfizer-BioNTech said it identified almost no safety signals and claimed the vaccine demonstrated over 91% “efficacy.”

Remarking on the documents, Brian Hooker, Ph.D., P.E., senior director of science and research for Children’s Health Defense, told The Defender:

“These adverse event reports are ‘off the charts,’ with myocarditis reports at over 10,000 and pericarditis reports at over 9,000.

“Historically, we know that this would be an under-ascertainment of the actual numbers. It is criminal for the EMA to keep this vaccine on the market.”

According to an analysis by commentator and author Daniel Horowitz, the percentage of adverse events classified as serious was “well above the standard for safety signals usually pegged at 15%,” and women reported adverse events at three times the rate of men.

Sixty percent of cases were reported with either “outcome unknown” or “not recovered,” suggesting many of the injuries “were not transient,” Horowitz said.

The highest number of cases occurred in the 31-50 age group, of which 92% did not have any comorbidities, making it very likely it was the vaccine causing “such widespread, sudden injury.”

There were 3,280 fatalities among vaccine recipients in the combined cumulative period including the clinical trials and post-marketing, up to July 18, 2022.

According to Horowitz, the documents “show that Pfizer knew about a sickening level of injury early on,” yet continued to distribute its COVID-19 vaccine.

The documents are not part of the ongoing court-ordered release of the so-called “Pfizer documents” in the U.S., but according to Horowitz, are pharmacovigilance documents requested by the EMA, the EU’s drug regulator.

The documents were made available to an Austrian science and politics blog, TKP, following “a FOIA [Freedom of Information Act] request from an anonymous reader.” They were subsequently published on March 4. However, once published, no European English-language media outlet appears to have reported on them.

As a result, they remained under the radar until recently, when several independent English-language bloggers discovered and published the documents.

Thousands of pediatric serious adverse events and deaths

The main Pfizer-BioNTech document revealed 9,605 adverse events (3,735 serious) during the PSUR #3 and 25 cases during the “clinical trials” among children ages 11 and younger. These included 20 fatalities, in children as young as 5 years old.

Causes of these fatalities included dyspnea, cardiac arrest, cardio-respiratory arrest, pyrexia and myocarditis, though “all events were assessed as unrelated” to the vaccine.

In one example listed in the document, an 11-year-old boy died of acute respiratory failure two days after the first dose of the vaccine. In another case, a 6-year-old girl died seven days following her initial dose of complications that included renal impairment, epilepsy, apnea, seizure and “sudden death.”

The document lists another case, that of a 6-year-old boy whose listed causes of death are myocarditis, cardio-respiratory arrest and COVID-19. He died seven days after the first dose of the vaccine, and although autopsy results were “pending,” “the reporter concluded that the death ‘had nothing to do’ with the administration of BNT162b2 [the Pfizer-BioNTech vaccine] and was due to natural causes.”

For children ages 12-17, the document listed 21,945 adverse eventss (19,558 serious) in the post-marketing period and 15 cases during clinical trials. A total of 169 deaths were recorded, with listed causes including dyspnea, pyrexia, cardiac arrest, myocarditis, cardiac failure, seizure and shock.

Nevertheless, the document states “No new significant safety information was identified based on the review of the cases reported in the overall paediatric population.”

‘No safety signals’ despites deaths, injuries of pregnant women and newborns

Pregnant and lactating women also were significantly affected. There were 3,642 post-authorization adverse events and 697 clinical trial adverse events in this population, including spontaneous abortion, fetal death, postpartum hemorrhage, premature separation of the placenta, premature labor or delivery, live birth with congenital anomalies and stillbirths.

Nevertheless, the documentation again states, “There were no safety signals regarding use in pregnant/lactating women that emerged from the review of these cases or the medical literature,” despite two key admissions elsewhere in the documentation.

In one instance, the document stated, “The safety profile of the vaccine in pregnant and/or breastfeeding women was not studied in the pivotal clinical trial and the maternal clinical trial was terminated early due to participant recruitment difficulties.”

And in another instance, Pfizer-BioNTech identified the following as “missing information”:

“Use in pregnancy and while breastfeeding; Use in immunocompromised patients; Use in frail patients with co-morbidities … Use in patients with autoimmune or inflammatory disorders; Interaction with other vaccines; Long term safety data.”

Pfizer-BioNTech stated a “commitment” to track “pregnancy outcome[s] in clinical trials.”

Myocarditis and pericarditis deaths among children, young adults

A notable discrepancy appears in terms of reported cases of myocarditis in the clinical trials as compared to the post-marketing period — one myocarditis case (0.15% of all cases) is listed for the clinical trial period, while 5,422 cases (1.1% of all cases) and 5,458 serious events were reported in the PSUR #3 period.

Of these, 87 cases were fatal and 1,608 were listed as “not resolved.” Among children and young adults, 48 cases were reported for those between the ages of 5 and 11 (two deaths), 366 among 12-15-year-olds (three deaths), 345 among 16-17-year-olds and 968 among 18-24-year-olds (four deaths).

In one instance, an 11-year-old girl developed myocarditis two days after her first dose and subsequently died, with the listed causes of death including myocarditis, respiratory failure, acute cardiac failure and cardio-respiratory arrest.

Separately, a 13-year-old boy developed myocarditis five days after his second dose, and subsequently died of myocarditis, cardiac arrest, multiple organ dysfunction syndromeventricular tachycardia and renal failure.

A 13-year-old girl with no medical history developed myocarditis six days after her first dose and also later died.

In the case of a 19-year-old male who developed myocarditis three days after his third dose and who eventually died, an autopsy “revealed extensive necrosis of the left ventricular myocardium (myocardial necrosis); myocarditis/fulminant myocarditis.”

And a 26-year-old male who also took the flu vaccine developed myocarditis four days after his third dose of the Pfizer-BioNTech COVID-19 vaccine, and subsequently died. The listed causes of death included myocarditis, arrhythmia, inflammation and left ventricular dysfunction. Autopsy results “showed myocarditis.”

Similarly, while no cases of pericarditis were recorded during the clinical trial, 4,156 were recorded during the PSUR #3 period, including 4,164 serious adverse events and 19 fatalities. This included 30 cases among 5-11-year-olds, 118 cases among 12-15-year-olds, 106 cases among 16-17-year-olds, 479 cases among 18-24-year-olds (and one death), and 417 cases among 25-29-year-olds, again including one death.

In one example, a 22-year-old male developed pericarditis 31 days after his second dose and eventually died of pericarditis and other causes, including multiple organ dysfunction syndrome, pericardial masspericardial effusionmalignant pericardial mesothelioma and right ventricular failure.

Numerous other cardiovascular adverse events were recorded, totaling 32,712 cases during the PSUR #3 period (496 fatal) and 27 during the clinical trials (two fatal — with none of the events listed as “related” to vaccination).

Causes of death included in this category include arrhythmia, cardiac failure and acute cardiac failure, cardiogenic shock, coronary artery disease, postural orthostatic tachycardia syndrome (POTS) and tachycardia.

Nevertheless, “No new significant safety information was identified.”

Many ‘very severe and very rare’ adverse events identified

The 393-page confidential Pfizer document shows that Pfizer observed more than 10,000 categories of diagnosis, many “very severe and very rare,” Horowitz wrote.

These include 73,542 cases of 264 categories of vascular disorders from the shots, many of which “are rare conditions,” hundreds of categories of nervous system disorders, totaling 696,508 cases and 61,518 adverse events from well over 100 categories of eye disorders, “which is unusual for a vaccine injury,” according to Horowitz.

In addition, “there were over 47,000 ear disorders, including almost 16,000 cases of tinnitus,” “roughly 225,000 cases of skin and tissue disorders,” “roughly 190,000 cases of respiratory disorders” and “over 178,000 cases of reproductive or breast disorders, including disorders you wouldn’t expect, such as 506 cases of erectile dysfunction.”

“Over 100,000 blood and lymphatic disorders, for both of which there’s a wealth of literature linking them to the spike protein” were indicated, as well as “almost 127,000 cardiac disorders, running the gamut of about 270 categories of heart damage, including many rare disorders, in addition to myocarditis.”

There were also “3,711 cases of tumors — benign and malignant,” and “there were over 77,000 psychiatric disorders observed.”

“What is so jarring is that there are hundreds of very rare neurological disorders that reflect something so systemically wrong with the shots, a reality that was clearly of no concern to the manufacturers and regulators alike,” Horowitz wrote, referencing 68 listed cases of a rare diagnosis, chronic inflammatory demyelinating polyneuropathy.

In another example, the “Pharma Files” Substack identified 3,092 neoplasms, noting that ”malignant neoplasms means cancer.”

Pfizer-BioNTech usually identified ‘no safety signal’ despite thousands of deaths

Numerous deaths and serious adverse events were recorded for a wide range of other conditions:

·     Stroke: 3,091 cases and 3,532 serious adverse events during PSUR #3, including 314 fatalities, and 19 cases during the clinical trial (one death).

The document stated, “Cerebral venous sinus thrombosis … and Cerebrovascular Accident/Stroke were evaluated as signals during the reporting period and were not determined to be risks causally associated with the vaccine … No additional safety signals … have emerged based on the review of these cases.”

·     Respiratory: 2,199 cases and 1,873 serious adverse events during PSUR #3, including 363 fatalities, and 33 cases during the clinical trial (four deaths). Serious adverse events included cardio-respiratory arrest, pneumonia, respiratory failure, acute respiratory failure, hypoxia and acute respiratory distress syndrome. Yet, “No safety signals have emerged based on the review of these cases.”

·     Bell’s palsy: 733 cases were reported during PSUR #3, in addition to 1,428 cases of facial paralysis. Six cases were fatal, with all victims over age 60. One additional case of Bell’s palsy, in a 75-year-old female from the U.S., was recorded in the clinical trial but was deemed “not related” to her vaccination. Again, “No new significant safety information was identified.”

·     Neurological: 5,111 cases and 4,973 serious adverse events during PSUR #3, including 67 fatalities, and 15 cases during the clinical trial. Once more, “No safety signals have emerged based on the review of these cases.”

·     Immune-mediated/autoimmune adverse events: 11,726 cases and 8,445 serious adverse events during PSUR #3, including 133 fatalities, and 19 cases during the clinical trial. Serious adverse events included thrombocytopeniainterstitial lung disease, cerebral hemorrhage, encephalitis, multiple organ dysfunction syndrome, renal failure, pneumonia and pulmonary embolism. Yet, “No new safety signals have emerged.”

·     Multisystem inflammatory syndrome: 207 cases and 210 serious adverse events during PSUR #3, including 56 deaths, with 35 involving the elderly. In addition, 38 cases were reported in children. Nevertheless, “No new safety signals have emerged based on a review of these cases [or] literature.”

Pfizer-BioNTech stated a “commitment” for “closely monitoring multisystem inflammatory syndrome in children and in adults … and reporting of new cases.”

·     Thromboembolic adverse events: 6,102 cases and 6,724 serious adverse events during PSUR #3, including 265 fatalities, and 17 cases during the clinical trial (one death). Serious adverse events included pulmonary embolism, thrombosis and deep vein thrombosis. Again, “No safety signals have emerged based on the review of these cases.”

Elsewhere in the document, the case of a 14-year-old male who died of peripheral swelling after getting the COVID-19 vaccine was mentioned, with no additional details.

In another example, a 67-year-old male “with a history of diabetes and idiopathic thrombocytopenic purpura” suffered chest and gastrointestinal discomfort less than 30 minutes after receiving his third dose of the vaccine. A diagnosis of anaphylaxis was made, while an electrocardiogram showed “signs of a myocardial infarction.” He later sustained cardiac arrest and died 12 days following his vaccination.

Moreover, 204 fatalities (and 24,077 cases) of vaccination failure, 81 deaths from “vaccination stress,” 24 deaths (and 1,402 cases) of suspected vaccination failure, two deaths from glomerulonephritis and nephrotic syndrome, two deaths (1,326 cases) from “medication error” and 166 deaths from “other” adverse events — mostly pyrexia — were recorded.

Pfizer-BioNTech and EMA: ‘nothing to see here’

Pfizer and BioNTech claimed that the overall efficacy of their COVID-19 vaccine for the PSUR #3 period was 91.3% — and 100% for some populations.

Moreover, only one safety signal was definitively identified: hearing loss, with Pfizer-BioNTech committing to perform a “safety evaluation of tinnitus and hearing loss.”

Two other conditions, myocarditis and pericarditis, were determined to be an “important identified risk,” while irritability was determined to be an “identified risk (not important).”

“A statement regarding the reporting rates of myocarditis and pericarditis after primary series and booster doses” was added to their vaccine’s European product label.

Labeling was changed for Guillain-Barré syndrome, but in Japan. The document stated:

“Although not considered by definition a regulatory action taken for safety reasons because it does not significantly impact the benefit risk balance of use of the product in authorised populations, due to the receipt of spontaneous reports of Guillain-Barre syndrome (GBS) after vaccination with mRNA COVID-19 vaccines including BNT162b2 … Japan has required class changes to include GBS in the important precautions section of the Japan package insert.”

Despite the large number of deaths and serious adverse events, Pfizer and BioNTech wrote, “Based on the available safety and efficacy/effectiveness data from the reporting interval for BNT162b2, the overall benefit-risk profile of BNT162b2 remains favorable” and that “no further changes … or additional risk minimization activities are warranted.”

The EMA appears to have agreed with this conclusion. In its “assessment report,” its Pharmacovigilance Risk Assessment Committee (PRAC) wrote that “The benefit-risk balance for the use of Comirnaty in its authorized indication remains unchanged.”

“The PRAC considers that the risk-benefit balance of medicinal products containing tozinameran (Comirnaty) remains unchanged and therefore recommends the maintenance of the marketing authorization(s),” the PRAC added.

However, Horowitz argues that the documents “show that Pfizer knew about a sickening level of injury early on,” yet continued to distribute its COVID-19 vaccine.

Earlier this month, BioNTech was sued in Germany by a woman alleging injuries from the Pfizer-BioNTech COVID-19 vaccine. The lawsuit demands at least 150,000 euro ($161,500) in damages for bodily harm and unspecified compensation for material damages.