Category: Science

This information comes from the CDC VAERS (Vaccine Adverse Event Reporting System) database. This information is accurate as of 14-Jun-2021. As usual, it must be mentioned that only approximately 1% of vaccine related injuries are reported to VAERS.

There are currently 3,045 events regarding the COVID-19 "vaccines" which contain the words 'blood' and 'clot'. Note that not all of them are related to blood clotting, however many are. Following are descriptions of a small fraction of these events.

0908959-1 Observed for 15 minutes after vaccine. About 30 minutes later in my car, felt sharp shooting pains in left neck. About 8 hours after receiving first dose, started coughing up blood, bright red, with streaks and clots. No cough, fever. Seen in ER with chest xray and ct scan with contrast. No resolve. On second day after receiving vaccine? Continue to experience bright red sputum. No resolve.

0910641-1 Weakness and tingling down left arm; Weakness and tingling down left arm; Lightheaded; PVC's every 3 beats; emotional too and just very tired; Can not read the vaccination card as she does not have her glasses; Palpitations; Fatigue; Slept a lot; Thready pulse and vertigo; Thready pulse and vertigo; Soreness in left arm at the injection site and down the left arm; Soreness in left arm at the injection site and down the left arm; This is a spontaneous report from a contactable nurse (patient). A 54-year-old female patient received first dose bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE, reason for no lot number of COVID Vaccine: Can not read the vaccination card as she does not have her glasses, Expiry Date unknown), via an unspecified route of administration in the left arm on 18Dec2020 at single dose for 'Work with COVID patients'. Medical history included none. There were no concomitant medications. The patient experienced weakness and tingling down left arm (hospitalization) on 22Dec2020, lightheaded (hospitalization) on 22Dec2020, PVC's every 3 beats (hospitalization) on 22Dec2020, soreness in left arm at the injection site and down the left arm on 18Dec2020, thready pulse and vertigo on 19Dec2020, fatigue on 20Dec2020, slept a lot on 19Dec2020, palpitations on 21Dec2020. Details as follows: Caller says she received the vaccine, she is a nurse. She got the vaccine on Friday, 18Dec2020. She had soreness in her arm and at the injection site on Friday but that was it. On Saturday (19Dec2020) she noticed a thready pulse, but went on with her day with only a little arm pain. Sunday (20Dec2020) she was fatigued and the thready pulse continued. She slept a lot on Saturday (19Dec2020) and Sunday (20Dec2020). Yesterday (21Dec2020) she felt a little better, but had palpitations here and there. This morning (22Dec2020) she went into work, was very lightheaded, had tingling down her left arm, and had palpitations. So she hooked herself up to a monitor. Her pulse ox was between 97-99%. Her heart rate would be in the 90s and then drop to 48, so she went down to the ED. She has had a CT, and she is throwing PVC's every 3 beets. She has not been admitted as they are still waiting for results. She is still in the ED. They did a CT to see if there was a possible clot. On 18Dec2020 she received the vaccine around 2 PM. She had soreness at the injections site and down the left arm, which went away by Sunday (20Dec2020). She now (22Dec2020) has weakness and tingling down the left arm. It was never red or anything at the injection site. Saturday, 19Dec2020, she had thready pulse and Vertigo which lasted until Sunday 20Dec2020. She would be laying in bed and try to flip to the other side and having vertigo. When the fatigue started on Sunday (20Dec2020) she did not feel like herself. She was very emotional too and just very tired. Since she went to the ED she has had a CT scan, one with contrast and one without. She had a chest X-ray, and she is on a cardiac monitor. Results are pending. She has Trigeminy PVCs. She says she never goes to the hospital. But she is not admitted yet (pending clarification). Can not read the vaccination card as she does not have her glasses. Unable to read off the NDC, lot, and expiration date. History: Has been on the same vitamins for two years with nothing new. Blood pressure: Normal base line is 130s/80s maybe lower. Heart rate: Currently within her normal limits of 80s-90s. Depending on what happens, it was asked if she should get the second dose. The patient underwent other lab tests and procedures which included blood pressure measurement: 163/76 on 22Dec2020, chest x-ray: unknown result on 22Dec2020 (Result: Pending), computerised tomogram (CT scan): unknown result on 22Dec2020 (Result: Pending), heart rate: 80s-90s on 22Dec2020, Pulse oximetry: 97-99 % on 22Dec2020, cardiac monitor: results are pending on 22Dec2020. The outcome of events weakness and tingling down left arm, pvc's every 3 beats, lightheaded, palpitations and fatigue was not recovered. The outcome of the event soreness in left arm at the injection site and down the left arm was recovered on 20Dec2020. The outcome of the events thready pulse and vertigo was recovered on 20Dec2020. The outcome of the event slept a lot was recovered on 20Dec2020. The outcome of other events was unknown. Information on the lot/Batch number has been requested.; Sender's Comments: Based on available information, a possible contributory role of the subject vaccine cannot be excluded for the reported events due to temporal relationship. There is limited information provided in this report. Additional information is needed to better assess the case, including complete medical history, diagnostics, counteractive treatment measures and concomitant medications. This case will be reassessed once additional information is available. The impact of this report on the benefit/risk profile of the Pfizer product is evaluated as part of Pfizer procedures for safety evaluation, including the review and analysis of aggregate data for adverse events. Any safety concern identified as part of this review, as well as any appropriate action in response, will be promptly notified to Regulatory Authorities, Ethics Committees and Investigators, as appropriate.

0916795-1 Soreness at injection site 3 hours post injection. 30 hours post injection, pt experiences a huge blood clot from vagina, about the circumference of a clementine. was not old blood, looked like frank blood. over the next 30 hours, pt experiences more clots, much smaller, about the size of a pea. pt has a headache and chills throughout. 48+ hours, experiencing what feels like menstrual cramps. no blood clots 72 hours post injection

0919376-1 Patient received Moderna vaccine, Wednesday 12/30. On Saturday 1/3/2021 patient felt pressure/tightness in lower extremity. When patient touched area, a noticeable ball was felt under the skin, tender to the touch and warm. Patient went into urgent care on Monday 1/4/2021 with a confirmed dx of a superficial blood clot. Unknown etiology of whether this is from current birth control or the COVID19 Moderna vaccine.

0923031-1 Worsening arm pain after injection that eventually resulted in my being diagnosed with a blood clot in the arm that I recevied the injection on

0924035-1 So I got the vaccine Monday night after work. Tuesday and Wednesday I ran a super high fever, body aches, lymphnode swelling on that side. No big deal . Well Thursday morning I woke up with a rash on both of my legs and my legs swollen like tree trunks. It?s a petechial rash. I called the pharmacist told to take Benadryl and Zyrtec since Friday. So I went to the doctors last night since I still have this rash and it hasn?t gotten any better with Benadryl and Zyrtec. I got blood work done today. And I have to get an arterial and venous Doppler done on Wednesday next week. They are concerned I may have blood clots since my legs are so swollen with a petechial rash. They are also giving me steroid tapper.

0925701-1 Blood clot in urine; Sore throat; Fever chills/chills; Fever; Headache; Vaginal bleeding; High temperature; This is a spontaneous report from a contactable other healthcare professional downloaded from the Medicines Agency (MA) Regulatory Authority-WEB GB-MHRA-WEBCOVID-20201218211718, Safety Report Unique Identifier GB-MHRA-ADR 24544990. A 33-year-old female non-pregnant patient received BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, batch/lot number: not known), via an unspecified route of administration on 16Dec2020 at a single dose for COVID-19 immunization. Medical history included abortion from Oct2020 to Oct2020. The patient's concomitant medications were not reported. The patient experienced blood clot in urine on 18Dec2020 with outcome of recovering, fever on 17Dec2020 with outcome of recovered on 17Dec2020, headache on 17Dec2020 with outcome of recovering, sore throat on 18Dec2020 with outcome of not recovered, fever chills/chills on 17Dec2020 with outcome of recovered on 17Dec2020, high temperature on 16Dec2020 with outcome of recovering, vaginal bleeding on 17Dec2020 with outcome of not recovered. The seriousness of all the events was medically significant. The patient underwent lab tests and procedures which included body temperature: 38.8 centigrade on unknown date, SARS-COV-2 test: no - negative covid-19 test on unknown date. Patient has not had symptoms associated with COVID-19. Patient is not enrolled in clinical trial. No follow-up attempts are possible. Information about lot/batch number cannot be obtained.

0930159-1 Strong stomach cramps leading to diarrhea, about 5 instances, followed by strong stomach cramping with blood clotting discharge with 9 instances, lasting about 16 hours, with the clotting reducing each time

0934745-1 Resident had seizure like activity followed by a vagel response with large bowel movement. Resident then began to show signs of blood clot to left lower extremity. No pedal pulse, area on leg warm to touch. Left lower leg now cold to touch, stiff, purple and white in color. No other signs of modeling, body warm to touch, no fever noted. Respirations and pulse increased with low oxygen levels. Resident not responding to stimuli.

0934907-1 "two skin procedures performed in his surgeons office the day before- one on his nose and one on his arm; nose was still slightly bleeding; This is a spontaneous report from a contactable consumer(patient). áA 72-year-old male patient received first dose of BNT162B2(PFIZER-BIONTECH COVID-19 VACCINE), via an unspecified route of administration on 30Dec2020 at single dose for COVID-19 immunization. Medical history included phlebotomy in Sep2020 because his blood was ""too thick"" and he had no history of a clotting problem until the time of the report.

0938147-1 I am not completely convinced that this is related to the vaccine but thought I should report it just in case. I thought I had a spider bite on my left foot, and then I thought it was shingles and then cellulitis. I was then diagnosed with a blood clot today. I have never had blood clots before.

0946743-1 She said she received her First Covid vaccine on 12/22/2020. She said on 1/4/2021 she worked that evening and started having severe pain in calf of her left leg no redness ,no heat, just hurt to work 1/8/2021 She had surgery on her left leg. 2nd Covid Vaccine received on 1/12/2021 She said she had PT on her right leg with severe pain in her left calf She said she did not have any therapy on her left leg. Two ? three hours later she developed chills, temp 100.1 took temp again later is was 99. She had ultrasound that showed a large blood clot She said the PA told her the blood clot could be from receiving the Covid vaccine

0946978-1 Onset of shortness of breath and cough on 1/3 that progressively got worse. Clinical diagnosis of pneumonia without fever was made, patient started azithromycin on 1/5 and albuterol treatments every 4-6 hrs. Initially he improved, but then worsened. chest xray on 1/6 was negative for pneumonia, PCR covid test was negative, albuterol treatment did not bring much relief. He started respiratory distress on 1/10 and was taken by car to the local ER where another covid test was negative and chest CT revealed multiple bilateral pulmonary emboli. The leg US revealed blood clots in both of his legs. He had an emergency catheter-delivered thrombolysis and was discharged home from the ICU on 1/12 on oral anticoagulants. He is gradually improving, but very weak. He tires easily and gets a drop in oxygen to 90- 93%, as well as an increase in the heart rate to 120 when walking less than half a mile. He runs out of breath with exertion.

0949555-1 Received Pfizer vaccine, first dose on Wed. 01/13/21 between 12 and 1 P.M. Thurs. 01/14/21 in the afternoon he began to note that he had difficultly walking. Went to bed when he woke up at 5:48 A.M. he reported he had ataxia. Patient reported having to walk in tiny steps to stay upright. He went to the emergency room. Had CT scan of head and found blood clots. MRI performed. Stroke found in right PCA territory, but no loss in strength in left lower extremity. Sensation and vision intact. Strength in all four extremities is 5 out of 5.

0950996-1 Constant headache began approximately 1 hr after receiving vaccine. Awoke this morning with blood clots on my tongue

0955638-1 Clot blood; This is a spontaneous report from a contactable consumer from the Medicines and Healthcare products Regulatory Agency (MHRA) with Regulatory authority report number GB-MHRA-WEBCOVID-20210105225534 and Safety Report Unique Identifier GB-MHRA-ADR 24560900. An 80-year-old female patient received BNT162B2 (lot/batch number and expiry date: not known), via an unspecified route of administration from 22Dec2020 to 22Dec2020 at single dose for COVID-19 vaccination. Medical history included lymphoedema from an unknown date. Concomitant medication included influenza vaccine (INFLUENZA VIRUS) for Influenza immunisation. On 25Dec2020, the patient's lymphedema arm had a blood clot, she required hospitalisation, antibiotics and blood thinners. Patient has not tested positive for COVID-19 since having the vaccine. Patient has not had symptoms associated with COVID-19. Patient is not enrolled in clinical trial. The patient underwent lab tests and procedures which included COVID-19 virus test: no - negative covid-19 test on an unknown date. The outcome of the event was recovering. No follow-up attempts are possible, information on lot/batch number cannot be obtained.

0957860-1 """I received the Pfizer Covid vaccine Wed afternoon around 4pm. Thursday morning around 9:30 I started with severe pain in my left leg. The pain worsened through the day and my leg began swelling. No other symptoms at all. This morning my leg was twice the size of my right leg so I went to the ER. I live in so I'm at ED. I have a massive blood clot running the the length of my leg - from my thigh to my ankle. I'm very lucky I got here so fast! I?m a very healthy 49 year old with no history of DVT or blood clots so they dug further to find out why. A cat scan showed I have a congenital condition called May Thurner Syndrome. I?m so relieved to have an answer and it?s fixable! The vascular doctors are not 100% convinced that?s not all that was going on as I was born with the syndrome and I?ve gone this long without a clot. So they are doing lots of labs to see if anything else shows up. This is where we are at. I?m being admitted to take care of the clot."""

0960219-1 "RESPIRATORY RATE HIGH; VOMITING; NAUSEA; ACUTE CORONARY SYNDROME; Cardiac thrombosis; This is a spontaneous report downloaded from the Agency Regulatory Authority-WEB NO-NOMAADVRE-FHI-2021-Uq8ag, Safety Report Unique Identifier NO-NOMAADVRE-E2B_00013788. A contactable physician reported that an 82-year-old female patient received bnt162b2 (COMIRNATY, lot number: EJ6795), via intramuscular route on 05Jan2021 at a single dose (first dose, administered into left arm) for covid-19 immunisation. Medical history included ongoing mental disorder, ongoing living in residential institution and ongoing hypercholesteremia. Concomitant medications included acetylsalicylic acid, magnesium oxide (ALBYL-E, 75 mg) administered via oral route, levothyroxine sodium (LEVAXIN, 100 ug), lithium sulfate (LITHIONIT, 83 mg) administered via oral route, citalopram hydrobromide (CIPRAMIL [CITALOPRAM HYDROBROMIDE], 10 mg) administered via oral route, cyanocobalamin, folic acid, pyridoxine (TRIOBE [CYANOCOBALAMIN;FOLIC ACID;PYRIDOXINE], 0.5 mg/0.8 mg/3 mg), and simvastatin (SIMVASTATIN SANDOZ, 40 mg), all from an unspecified date in 2019 to an unspecified date in 2021 for unknown indication. The patient experienced respiratory rate high, vomiting, nausea and acute coronary syndrome (ACS), all on 06Jan2021 with fatal outcome. The patient underwent lab tests on 06Jan2021 which included blood pressure measurement: drop in blood pressure and oxygen saturation: drop in oxygen saturation. The patient died on 06Jan2021. An autopsy was performed that revealed cardiac thrombosis (intracardiac thrombus) as the cause of death. The Regional Pharmacovigilance Center has assessed the causal relationship between the suspect product and respiratory rate high, vomiting and nausea as Possible, and causal relationship between the suspect product and acute coronary syndrome as Unlikely. Reporter's comment: The patient developed nausea and vomiting 24 hours later. Subsequent frequent superficial respiration with BT (blood pressure) and SAT (oxygen saturation) fall. Clinical suspicion of ""ACS syndrome (reported as AKS)"". 15-Jan-2021 RELIS: additional information received by telephone: Patient with comorbidity psychiatric disorder, hypercholestrolemia, reduced functional level. No known heart failure at time of vaccination. Residence at nursing home not considered as terminal, hard to say but expected lifetime about 1.5 years. Preliminary autopsy report concludes: CARDIAC THROMBOSIS cause of death. Sender's comments (Health Authority comments): ""The report concerns a nursing home resident with several underlying diseases who, within 24 hours after vaccination, developed nausea, vomiting and hyperventilation, interpreted as a possible ACS. Information has been obtained from a temporary autopsy report where a blood clot in the heart has been detected. When vaccinating marginal patients who are ill with many underlying diseases, some serious events, including death, may occur shortly after vaccination without any connection to vaccination. It is difficult to imagine how the vaccine can cause a blood clot in the heart within a day. The patient had several underlying risk factors for ischemic heart disease, and it is considered that these are more likely to have caused the reported symptoms. However, it cannot be ruled out that the vaccine has contributed to some of the symptoms, as nausea and vomiting are known side effects of the vaccine. Nor can it be ruled out that side effects of the vaccine have led to a worsening of the patient's underlying diseases"". No follow-up attempts are possible. No further information is expected.; Reported Cause(s) of Death: respiratory rate high; vomiting; nausea; acute coronary syndrome; CARDIAC THROMBOSIS; Autopsy-determined Cause(s) of Death: CARDIAC THROMBOSIS"

This information comes from the CDC VAERS (Vaccine Adverse Event Reporting System) database. This information is accurate as of 13-Jun-2021. As usual, it must be mentioned that only approximately 1% of vaccine related injuries are reported to VAERS.

There are currently 797 events regarding the COVID-19 "vaccines" which contain the word 'memory'. Note that not all of them are related to memory problems, however many do mention memory loss and cognitive problems. Following are descriptions of a small fraction of these events.

0907129-1 Headache, nausea, dizziness, lightheadedness, lack of concentration and memory issues

0913226-1 Short-term memory loss consistent with Transient Global Amnesia

0918826-1 Delirium and cognitive dysfunction, memory loss. Trouble concentrating. High fever, body aches, headache. Delirium subsided after 2 days. High fever, body aches and headache went away after 3 days. Cognitive difficulty and memory loss persist.

0920237-1 having short term memory/can not recall things from 2 months ago; soreness in arm; This is a spontaneous report from a contactable Physician. A female patient (Reporter's wife) of unspecified age received BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE) at single dose on unknown date for COVID-19 immunization. Relevant medical history and concomitant medications were not reported. On 29Dec2020 the patient experienced soreness in arm and at 4 o'clock pm she having short term memory, cannot recall things from 2 months ago. The outcome of the events was reported as unknown. Information on the lot/batch number has been requested.

0926310-1 I had visual aura with migraine which is a normal event for me. This time, however, it was accompanied by confusion and memory loss that lasted about 15 minutes. I couldn?t say names of people known to me or read a list on my counter. In 25 years of migraines I have never had these symptoms with my migraine. I took an over the counter migraines medicine which resolved the symptoms.

0930775-1 Severe musculoskeletal pain, severe fatigue, poor memory, poor cognitive function, weight loss, loss of appetite, injection site pain

0930839-1 Confusion, disorientation, memory loss, nausea, vomiting, brief episode, approximately 2 hours

0934906-1 "experienced symptoms of TIA; Severe aphasia; blurred vision; confusion; short term memory loss; elevated blood pressure; This is a spontaneous report from a contactable Other-HCP(Patient). A 57-year-old female patient received first dose of BNT162B2(PFIZER-BIONTECH COVID-19 VACCINE), via an unspecified route of administration at right arm, on 22Dec2020 08:15 at single dose for COVID-19 immunization. The patient was not pregnant. Medical history included herpes simplex on lips, post menopause, elevated cholesterol w/lifestyle changes. Known allergies reported as no. Concomitant medication included varicella zoster vaccine rge (cho) (SHINGRIX) for immunization. On 04Jan2021 08:30, the patient experienced symptoms of transient ischaemic attack(TIA), severe aphasia, blurred vision, confusion, short term memory loss, elevated blood pressure. The patient admitted to (Hospital name) (still here, hospitalization days reported as 2). Symptoms resolved except very mild aphasia. The patient had very few risk factors for TIA but did have family history of cardiovascular(CV) disease at young age, low density lipoprotein(LDL) was 192. The patient did not have diabetes, HTN, or known heart disease. She did not have severe anxiety. She did not smoke or use any substances. She walked about five miles 4x a week. Weigh reported as 157. Events reported as serious due to hospitalization. The patient had no Covid prior vaccination. Covid(nasal swab) was tested post vaccination on 04Jan2021, Covid test result was Negative. The event resulted in emergency room/department or urgent care. Treatment received for the adverse event included clopidogrel bisulfate(PLAVIX), acetylsalicylic acid (ASPIRIN), statin; potassium, CT, MRI, ""telemet"". The outcome of the events was recovering. Information on the lot/batch number has been requested.; Sender's Comments: The Company cannot completely exclude the possible causality between the reported symptoms of transient ischaemic attack(TIA), severe aphasia, blurred vision, confusion, short term memory loss, elevated blood pressure and the administration of BNT162B2, based on the reasonable temporal association. The impact of this report on the benefit/risk profile of the Pfizer product is evaluated as part of Pfizer procedures for safety evaluation, including the review and analysis of aggregate data for adverse events. Any safety concern identified as part of this review, as well as any appropriate action in response, will be promptly notified to RA, Agency, as appropriate."

0936202-1 some memory loss; locked jaw/unable to open mouth; her arm hurt; pain went in her jaws; she was really scared; Excruciating pain on left ear; swelling in arm; This is a spontaneous report from a contactable other healthcare professional. A 62-year-old female patient received BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE; Batch/lot number: ES1685, Expiry date: 01Mar2021) via intramuscular (left deltoid) on 28Dec2020 at single dose for COVID-19 immunization. The patient medical history and concomitant medications were not reported. She stated she is very healthy and don't have any medical conditions. She further stated that it was a scary moment, she don't want to take any chances, she was really frightened (28Dec2020). She made a complaint to let know her experience with the vaccine. Her cousin took the vaccine and told her she needed to report these events. The patient stated she experienced side effects after the first dose of the vaccine: Excruciating pain on left ear, locked jaw, her left upper arm was hurting on 28Dec2020. The pain went in her jaws and she was unable to open her mouth on 28Dec2020. She took 2 Benadryl and it relieved her. She saw on television if you experienced any side effects to take Benadryl. She also took Tylenol for the pain. She also had swelling in arm on an unspecified date in Dec2020. She also experienced some memory loss described as short-term memory loss on 30Dec2020. She stayed in bed after the vaccine, she was really scared, and stated she had memory loss and she don't have any memory problems. She was unable to remember if her car was black. She was looking for a white car. She drives a black car. She stayed in bed all day on Tuesday. Patient was asking what will happen if she does not take the second vaccine. The same morning while she was waiting to get the vaccine, a co-worker sent her a video of a woman who had received a COVID vaccine. She does not know which one. The woman experienced Bell's Palsy. The woman was crying and her face was turning side ways. She stated some people were talking negatively about the vaccine. She stated doesn't want her face to be deformed. She stated what are the cons of not taking the second vaccine. Reporter assessed the events as non-serious. Outcome of the events some memory loss and locked jaw/unable to open mouth was recovered on 30Dec2020, outcome of the events excruciating pain on her left ear, pain went in her jaws, her arm was hurt was recovering. Outcome of swelling in arm and she was really scared was unknown.

0937556-1 EXTREME VERTIGO, HIGH FEVERS, SYNCOPE, BODY ACHES, CHILLS, MEMORY LOSS

0955231-1 "After receiving Moderna vaccine, pt became increasingly tired, withdrawn, and confused, refusing to walk at home. He has begun to have mild memory changes after suspected COVID illness (covid testing negative) in November, but daughter of patient, with whom he lives, states that his memory and orientation now significantly changed- he seems to have forgotten the last ""3 years"" of memory. Presented to ER 1/16/21 as she checked his O2 and found him to be hypoxic in 60s. He is being treated for possible CAP with underlying perviously undiagnosed ILD vs post-covid lung changes (per pulmonology), and his energy and ability to walk have returned but memory is significantly impaired, confabulating and oriented only to self despite good oxygenation on 5L O2 by NC."

0955911-1 Approximately 3 days after my injection I began experience severe tremors Ib bilateral arms, bilateral legs, head, and vocal cord tremors as well as blurry vision and memory impairment. Unfortunately, the symptoms don't seem to be improving. My MD prescribed metoprolol, which I will begin today.

0956615-1 Two days after my wife received the moderna vaccine she showered significant cognitive impairment and memory loss . She cannot recall words and is experiencing delirium. Both her internist and her neurologist are convinced it was the result of the vaccine e. She had a complete Nueromosych evaluation done two months ago snd the results were completed normal. I want you to be aware of this snd if it does not resolve I may sue the federal government and moderna. Thanks a llot

0959476-1 Around 30 minutes after vaccine, I started to feel dizzy and light headed As the day went on, I started to get a headache and get very tired. Then around 5 I started to feel intense: Headache Chills/cold Dizzy/light headed/almost fell over several times Muscle weakness, could not carry anything or lift Muscles in face felt like they were melting down/stroke sensation Exhaustion Sore/achy everywhere Tender left arm where shot was Could not think/memory was gone/could not put together a sentence Tightness chest/hard to breath Could not keep eyes open Had to lay down and sleep with long pants long sweater, jacket and 3 blankets I woke up the next morning and some of my symptoms were gone except I still felt tired and had some achy ness, pain and left arm hurt and had shooting pain in joints Shooting severe pain in each joint, laster for 3 days, most severe in joints where I received vaccine but also in wrists, shoulder, elbows, hips, knees, ankles At day 5 my left arm is still sore including muscles around injection site

0960435-1 Internal brain bleeding 10 days after 1st dose covid vaccine; Brain damage; confused; suffering memory loss; This is a spontaneous report from a contactable Physician (patient). This 39-year-old female patient received the 1st dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE) intramuscular on 18Dec2020 14:30 at single dose (lot number: EJ1685) for covid-19 immunisation. Medical history and concomitant medications were unknown. The patient experienced internal brain bleeding and brain damage on 30Dec2020 07:30 after 1st dose covid vaccine. Brain surgery received on 29Dec2020. Events were still recovering. Patient was confused and suffering memory loss on 30Dec2020 07:30. Events resulted in Doctor or other healthcare professional office/clinic visit, Emergency room/department or urgent care, Hospitalization, Prolongation of existing hospitalization (vaccine received during existing hospitalization), Life threatening illness (immediate risk of death from the event), disability or permanent damage. Days for hospitalization was 16. The patient received treatment for events as brain surgery due to internal brain bleeding. The patient was not pregnant. The patient had no COVID prior vaccination, no COVID tested post vaccination. Outcome of the events was recovering.; Sender's Comments: The reported internal brain bleeding and brain damage with confused and memory loss more likely represented intercurrent disease, and less likely causally related to 1st dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE). The case will be reassessed should additional information become available. The impact of this report on the benefit/risk profile of the Pfizer product is evaluated as part of Pfizer procedures for safety evaluation, including the review and analysis of aggregate data for adverse events. Any safety concern identified as part of this review, as well as any appropriate action in response, will be promptly notified to Regulatory Authorities, Ethics Committees and Investigators, as appropriate.

0962397-1 "Morning after receiving vaccine (01/14/2021), woke up and was having chills, weakness, ""head felt like it did when having covid, dizziness, light-headed"". Urinary incontinence and memory loss, and hallucinations on 01/14/2021. Blue color to left deltoid started 01/13/2021 in PM and on 01/14/2021 when waking up, left upper arm was blue and redness noted down to elbow. ""I have laid on the couch and that's basically all I've done since getting the shot.""

0962422-1 "Left deltoid began turning blue evening of 01/13/2021. After awakening on 01/14/2021, left upper arm was blue and red to elbow. Voices that ""head felt like it did when I had covid, light-headed, dizziness"", hallucinations, urinary incontinence, weakness, memory loss."

0974416-1 First 24 hours sore arm and felt achy and out of it. Thought I was starting to feel myself by Sunday midday but then suddenly on Sunday afternoon almost exactly 48 hours after the shot I started to feel extreme confusion and short term memory loss. My body started shaking, I felt very hot and then very cold (back and forth) and began experiencing shortness of breath. It was all very scary and I ended up in the ER.