Found 501 cases where Vaccine targets COVID-19 (COVID19) and Patient Died
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| VAERS ID:940954 (history) Form:Version 2.0 Age:82.0 Sex:Female Location:Louisiana Vaccinated:2021-01-05Onset:2021-01-05 Days after vaccination:0Submitted:0000-00-00Entered:2021-01-13Vaccination / ManufacturerLot / DoseSite / RouteCOVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH- / 1LA / –Administered by: Private Purchased by: ? Symptoms: Chest pain, Cold sweat, Death, Dyspnoea, Myocardial infarction SMQs:, Anaphylactic reaction (broad), Myocardial infarction (narrow), Embolic and thrombotic events, arterial (narrow), Acute central respiratory depression (broad), Pulmonary hypertension (broad), Gastrointestinal nonspecific symptoms and therapeutic procedures (broad), Cardiomyopathy (broad), Hypoglycaemia (broad)Life Threatening? No Birth Defect? No Died? Yes Date died: 2021-01-05 Days after onset: 0 Permanent Disability? No Recovered? No Office Visit? No ER Visit? No ER or Doctor Visit? No Hospitalized? No Previous Vaccinations: Other Medications: Current Illness: Preexisting Conditions: Allergies: Diagnostic Lab Data: CDC Split Type: USPFIZER INC2021015421Write-up: Heart attack; This is a spontaneous report from a contactable consumer. An 82-year-old female patient received the first dose of bnt162b2 (PFIZER-BIONTECH COVID-19 MRNA VACCINE; Lot Number: and Expiration Date: Unknown), via an unspecified route of administration in the left arm on 05Jan2021 at 13:00 at a single dose for COVID-19 immunization; administered in doctor”s office/urgent care. The patient”s medical history and concomitant medications were not reported. It was unknown if the patient received any other vaccines within four weeks prior to the COVID vaccine. Prior to the vaccination, the patient was not diagnosed with COVID-19. Since the vaccination, the patient had not been tested for COVID-19. On 05Jan2021, the patient experienced heart attack; which resulted in death and was assessed as medically significant. The patient also experienced the associated symptoms of cold sweats, chest pain, shortness of breath. Therapeutic measures were taken as a result of heart attack, which included “life saving measures” by the paramedics performed upon arrival with no success. The clinical outcome of the event, heart attack, was fatal. The patient died on 05Jan2021 due to heart attack; as ruled by the paramedics. It was unknown if an autopsy was performed. The batch/lot numbers for the vaccine, PFIZER-BIONTECH COVID-19 MRNA VACCINE, were not provided and will be requested during follow up.; Reported Cause(s) of Death: Heart attack |
| VAERS ID:940955 (history) Form:Version 2.0 Age:66.0 Sex:Female Location:New York Vaccinated:2021-01-11Onset:2021-01-11 Days after vaccination:0Submitted:0000-00-00Entered:2021-01-13Vaccination / ManufacturerLot / DoseSite / RouteCOVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECHEL1284 / 2LA / OTAdministered by: Other Purchased by: ? Symptoms: Autopsy, Cardiac arrest, Death, Pulse absent, Respiratory arrest, SARS-CoV-2 test negative SMQs:, Torsade de pointes/QT prolongation (broad), Anaphylactic reaction (narrow), Arrhythmia related investigations, signs and symptoms (broad), Shock-associated circulatory or cardiac conditions (excl torsade de pointes) (narrow), Acute central respiratory depression (narrow), Guillain-Barre syndrome (broad), Cardiomyopathy (broad), Hypersensitivity (broad), Respiratory failure (narrow), COVID-19 (broad)Life Threatening? No Birth Defect? No Died? Yes Date died: 2021-01-11 Days after onset: 0 Permanent Disability? No Recovered? No Office Visit? No ER Visit? No ER or Doctor Visit? No Hospitalized? No Previous Vaccinations: Other Medications: ; ; EFFEXOR; ; ABILIFY; ; CRANBERRY; ; TYLENOL; ; LASIX [FUROSEMIDE]; IPRATROPIUM/ALBUTEROL; ; SENNA [SENNA ALEXANDRINA LEAF]; POLYETHYLENE GLYCOL 3350; Current Illness: Preexisting Conditions: Medical History/Concurrent Conditions: COVID-19 (Prior to vaccination, the patient was diagnosed with COVID-19); Diastolic heart failure; Epilepsy; Morbid obesity; Pulmonary hypertension; Spinal stenosis Allergies: Diagnostic Lab Data: Test Date: 20210111; Test Name: pulseless; Result Unstructured Data: Test Result:pulseless; Test Date: 20210111; Test Name: breathless; Result Unstructured Data: Test Result:breathless; Test Date: 20210106; Test Name: Covid-19 PCR; Result Unstructured Data: Test Result:Negative (Nasal Swab) CDC Split Type: USPFIZER INC2021018488Write-up: Cardiac Arrest; Patient was found pulseless and breathless 20 minutes following the vaccine administration.; Patient was found pulseless and breathless 20 minutes following the vaccine administration.; This is a spontaneous report from a contactable other healthcare professional (HCP). A 66-year-old female patient (pregnant at the time of vaccination: no) received the second dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, lot number: EL1284) via intramuscular at left arm on 11Jan2021 12:15 PM at single dose for COVID-19 immunization. Medical history included diastolic CHF, spinal stenosis, morbid obesity, epilepsy, pulmonary hypertension and COVID-19 (Prior to vaccination, the patient was diagnosed with COVID-19). The patient received medication within 2 weeks of vaccination included amiodarone, melatonin, venlafaxine hydrochloride (EFFEXOR), ibuprofen, aripiprazole (ABILIFY), lisinopril, cranberry capsules, diltiazem, paracetamol (TYLENOL), famotidine, furosemide (LASIX [FUROSEMIDE]), ipratropium bromide, salbutamol sulfate (IPRATROPIUM/ALBUTEROL), buspirone, senna alexandrina leaf (SENNA [SENNA ALEXANDRINA LEAF]), polyethylene glycol 3350 and morphine. The patient did not receive any other vaccines within 4 weeks prior to the COVID vaccine. Patient used took Penicillin, propranolol, quetiapine, topiramate, Lamictal and had allergy to them. Patient used took the first dose of BNT162B2 (lot number: EJ1685) via intramuscular at right arm on 21Dec2020 12:00 PM at single dose for COVID-19 immunization. Since the vaccination, the patient been tested for COVID-19 (Sars-cov-2 PCR) via nasal swab on 06Jan2021, covid test result was negative. Patient was found pulseless and breathless 20 minutes following the vaccine administration (11Jan2021 12:30 AM). MD found no signs of anaphylaxis. Patient died on 11Jan2021 12:30 AM because of cardiac arrest. No treatment received for the events. Outcome of pulseless and breathless was unknown. the autopsy was performed, and autopsy remarks was unknown. Autopsy-determined cause of death was unknown. It was reported as non-serious, not results in death, Life threatening, caused/prolonged hospitalization, disabling/Incapacitating nor congenital anomaly/birth defect.; Sender”s Comments: Based on the available information this patient had multiple underlying medical conditions including morbid obesity, diastolic CHF, epilepsy, pulmonary hypertension and COVID-19 diagnosed prior to vaccination. All these conditions more likely contributed to patients cardiac arrest resulting in death. However, based on a close temporal association (“Patient was found pulseless and breathless 20 minutes following the second dose of BNT162B2 vaccine administration, contributory role of BNT162B2 vaccine to the onset of reported events cannot be completely excluded. 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.; Reported Cause(s) of Death: Cardiac arrest; Autopsy-determined Cause(s) of Death: autopsy remarks was unknown. Autopsy-determined cause of death was unknown |
| VAERS ID:941215 (history) Form:Version 2.0 Age:90.0 Sex:Female Location:Unknown Vaccinated:2021-01-06Onset:2021-01-08 Days after vaccination:2Submitted:0000-00-00Entered:2021-01-13Vaccination / ManufacturerLot / DoseSite / RouteCOVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH- / 1- / –Administered by: Unknown Purchased by: ? Symptoms: Death, Syncope SMQs:, Torsade de pointes/QT prolongation (broad), Arrhythmia related investigations, signs and symptoms (broad), Cardiomyopathy (broad), Hypotonic-hyporesponsive episode (broad), Hypoglycaemia (broad)Life Threatening? No Birth Defect? No Died? Yes Date died: 2021-01-08 Days after onset: 0 Permanent Disability? No Recovered? No Office Visit? No ER Visit? No ER or Doctor Visit? No Hospitalized? No Previous Vaccinations: Other Medications: Current Illness: Preexisting Conditions: Medical History/Concurrent Conditions: Aortic valve replacement (Verbatim: Aortic valve replacement) Allergies: Diagnostic Lab Data: CDC Split Type: USPFIZER INC2021018269Write-up: Actual event and cause of death were unknown; This is a spontaneous report from a non-contactable consumer. A 90-year-old female patient received first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE), via an unspecified route of administration on 06Jan2021 at single dose for COVID Prevention. The relevant medical history included aortic valve replacement from Nov2019. Concomitant medications were not reported. The consumer stated that she was taking the reporting responsibilities to report that a friend of hers, informed that the patient passed away on Friday, and had received the COVID vaccine on Wednesday. The consumer stated that it was unknown to her at this time, if the friend had called to complete a report herself, regarding the incident. Their conversation was very brief. The patient was 90 years old, and it was her friend”s mother that was the patient. Actual event and cause of death were unknown. The patient had her vaccine on Wednesday 06Jan2021, and then the patient collapsed in front of the reporter at Friday night on 08Jan2021 and passed away that same day. The autopsy was unknown. The outcome of the event was fatal. No follow-up attempts are possible; information about lot/batch number cannot be obtained.; Reported Cause(s) of Death: Actual event and cause of death were unknown |
| VAERS ID:941561 (history) Form:Version 2.0 Age:91.0 Sex:Male Location:Minnesota Vaccinated:2021-01-07Onset:2021-01-08 Days after vaccination:1Submitted:0000-00-00Entered:2021-01-13Vaccination / ManufacturerLot / DoseSite / RouteCOVID19: COVID19 (COVID19 (MODERNA)) / MODERNA011L20A / UNKLA / IMAdministered by: Senior Living Purchased by: ? Symptoms: Cerebrovascular accident, Death, Decreased appetite, Grip strength decreased, Hemiplegia, Hypotonia, Speech disorder, Weight decreased SMQs:, Peripheral neuropathy (broad), Hyperglycaemia/new onset diabetes mellitus (broad), Ischaemic central nervous system vascular conditions (narrow), Haemorrhagic central nervous system vascular conditions (narrow), Dementia (broad), Embolic and thrombotic events, vessel type unspecified and mixed arterial and venous (narrow), Psychosis and psychotic disorders (broad), Guillain-Barre syndrome (broad), Noninfectious encephalitis (broad), Noninfectious encephalopathy/delirium (broad), Conditions associated with central nervous system haemorrhages and cerebrovascular accidents (narrow), Hypotonic-hyporesponsive episode (broad), Generalised convulsive seizures following immunisation (broad)Life Threatening? No Birth Defect? No Died? Yes Date died: 2021-01-11 Days after onset: 3 Permanent Disability? No Recovered? No Office Visit? No ER Visit? No ER or Doctor Visit? No Hospitalized? No Previous Vaccinations: Other Medications: Escitalopram Oxalate, Metformin ER, Systane balance, Colace, Refresh tears, Milk of Magnesia, Diltiazem Current Illness: Resident was on hospice for Alzheimer”s disease. Preexisting Conditions: Alzheimer”s Disease, Type II diabetes, Major depression disorder, Elevated B/P readings with Hypertension, history of stroke (7/22/2019 – Acute Lacunar Stroke) Allergies: No known Allergies Diagnostic Lab Data: Resident was declining for some time. He normally had a high heart rate. Appetite was poor with a significant weight loss noted. CDC Split Type:Write-up: Staff walked into resident”s room around 10:00am and noted resident”s left side of his face was flaccid. Nurse was called and upon assessment resident noted to have an unequal hand grasp with left worse. He was able to talk but was mumbled and hard to understand. Physician, hospice, and family were notified. Resident had a stroke at 10:06 am on 1/8/2020. He lost all ability to use his left side. Resident passed away on 1/11/2020. |
| VAERS ID:941607 (history) Form:Version 2.0 Age:83.0 Sex:Female Location:Indiana Vaccinated:2021-01-12Onset:2021-01-13 Days after vaccination:1Submitted:0000-00-00Entered:2021-01-13Vaccination / ManufacturerLot / DoseSite / RouteCOVID19: COVID19 (COVID19 (MODERNA)) / MODERNA032H20A / 1RA / IMAdministered by: Senior Living Purchased by: ? Symptoms: Anal incontinence, Death, Hypotonia, Unresponsive to stimuli SMQs:, Peripheral neuropathy (broad), Hyperglycaemia/new onset diabetes mellitus (broad), Neuroleptic malignant syndrome (broad), Guillain-Barre syndrome (broad), Noninfectious encephalitis (broad), Noninfectious encephalopathy/delirium (broad), Noninfectious meningitis (broad), Hypotonic-hyporesponsive episode (broad), Generalised convulsive seizures following immunisation (broad), Noninfectious diarrhoea (broad), Hypoglycaemia (broad)Life Threatening? No Birth Defect? No Died? Yes Date died: 2021-01-13 Days after onset: 0 Permanent Disability? No Recovered? No Office Visit? No ER Visit? No ER or Doctor Visit? No Hospitalized? No Previous Vaccinations: Other Medications: Tylenol 325mg, Lasix 20mg, Senna 8.6mg, Aspirin 81mg, Levothyroxine 75mcg Current Illness: N/A Preexisting Conditions: End stage dementia, cerebro vascular disease, Hx left vertebral artery aneurysm Allergies: NKA Diagnostic Lab Data: N/A CDC Split Type:Write-up: The patient passed away today, 1/13/2021. She was a hospice patient. She showed no adverse effects after receiving the vaccine on 1/12/2021. This morning she woke up as normal and during her morning shower she had a bowel movement, went limp and was non-responsive. The patient passed away at 7:45 am. |
| VAERS ID:941743 (history) Form:Version 2.0 Age:60.0 Sex:Female Location:New York Vaccinated:2021-01-12Onset:2021-01-13 Days after vaccination:1Submitted:0000-00-00Entered:2021-01-13Vaccination / ManufacturerLot / DoseSite / RouteCOVID19: COVID19 (COVID19 (MODERNA)) / MODERNA011J20A / 1RA / IMAdministered by: Other Purchased by: ? Symptoms: Death SMQs:Life Threatening? No Birth Defect? No Died? Yes Date died: 2021-01-13 Days after onset: 0 Permanent Disability? No Recovered? No Office Visit? No ER Visit? No ER or Doctor Visit? No Hospitalized? No Previous Vaccinations: Other Medications: Amitiza, Anastrozole, Calcium Carbonate, Levemir, Novolog, Docusate, Fiber Lax, Fluvoxamine Maleate, Gavilax, Glucerna, Ketoconazole, levetiracetam, loratadine, Selenium sulfide lotion, vimpat, vitamin D3, Prolia AS needed medications: fle Current Illness: None Preexisting Conditions: Benign polycythemia, Type II DM, Anxiety, Epilepsy, Blepharitis (bilateral), cataract (not specified), Allergic rhinitis, constipation, scoliosis, osteoporosis, dyspahgia, urinary incontinence, Dermatitis, breast cancer (right breast lumpectomy), history of respiratory infection, DNR AND MOLST were in place at time of death Allergies: No known drug or food allergies Diagnostic Lab Data: None CDC Split Type:Write-up: This person was found to be deceased on routine rounds during the night, 3am. No symptoms of reaction noted post vaccine. No injection site reaction. No reports of any allergic reaction. |
| VAERS ID:941811 (history) Form:Version 2.0 Age:56.0 Sex:Female Location:Louisiana Vaccinated:2021-01-04Onset:2021-01-11 Days after vaccination:7Submitted:0000-00-00Entered:2021-01-13Vaccination / ManufacturerLot / DoseSite / RouteCOVID19: COVID19 (COVID19 (MODERNA)) / MODERNA011J20A / 1LA / IMAdministered by: Senior Living Purchased by: ? Symptoms: Albumin urine present, Bacterial test positive, Chest X-ray abnormal, Death, Hypoxia, Lung infiltration, Pyrexia, Respiratory distress, Respiratory failure, SARS-CoV-2 test negative, Sepsis, Urine leukocyte esterase positive, White blood cell count normal, White blood cells urine positive SMQs:, Anaphylactic reaction (broad), Asthma/bronchospasm (broad), Interstitial lung disease (narrow), Neuroleptic malignant syndrome (broad), Anticholinergic syndrome (broad), Shock-associated circulatory or cardiac conditions (excl torsade de pointes) (broad), Torsade de pointes, shock-associated conditions (broad), Hypovolaemic shock conditions (broad), Toxic-septic shock conditions (broad), Anaphylactic/anaphylactoid shock conditions (broad), Hypoglycaemic and neurogenic shock conditions (broad), Acute central respiratory depression (narrow), Pulmonary hypertension (broad), Guillain-Barre syndrome (broad), Cardiomyopathy (broad), Eosinophilic pneumonia (broad), Chronic kidney disease (broad), Hypersensitivity (broad), Proteinuria (narrow), Tubulointerstitial diseases (broad), Respiratory failure (narrow), Drug reaction with eosinophilia and systemic symptoms syndrome (broad), Infective pneumonia (broad), Hypokalaemia (broad), Sepsis (narrow), Opportunistic infections (broad), COVID-19 (broad)Life Threatening? No Birth Defect? No Died? Yes Date died: 0000-00-00 Permanent Disability? No Recovered? No Office Visit? No ER Visit? No ER or Doctor Visit? No Hospitalized? No Previous Vaccinations: Other Medications: Haldol 2mg TWICE DAILY, DEPAKENE 750MG THREE TIMES Current Illness: NONE Preexisting Conditions: HUNTINGTON”S CHOREA, HTN, HLP, HYPOTHYROID, DEPRESSION, CONSTIPATION, AND DYSPHAGIA Allergies: NKDA & NO FOOD ALLERGIES Diagnostic Lab Data: CXR on 1/11/21: Suspicion of minimal infrahilar infiltrates bilaterally. U/A on 1/11/21: Leuk Esterase 3+, Albumin 2+, Few Bacteria, White cells 10 CBC on 1/11/21: WBC 8.9 CDC Split Type:Write-up: Resident began having fever on 1/11/21 @0600. VS= T-102 B/P- 100/57 P- 112 RR- 24 O2 Sat 92% on RA. MD called. Rapid COVID Test was negative. CBC,CMP, U/A were ordered as well as CXR. Resident”s condition declined. At 3:00pm resident started having respiratory distress and hypoxia O2 Sat 89%. Supplemental O2/mask @ 5LPM. Neb TX, EKG, and Rocephin 1 GM ordered. Condition worsened. Resident sent to nearest ER for evaluation. Later in the evening the staff AT Medical Center called to inform staff that resident had expired @ 2230 as a result of Respiratory Failure and Sepsis. |
| VAERS ID:942040 (history) Form:Version 2.0 Age:78.0 Sex:Male Location:Iowa Vaccinated:2021-01-13Onset:2021-01-13 Days after vaccination:0Submitted:0000-00-00Entered:2021-01-13Vaccination / ManufacturerLot / DoseSite / RouteCOVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECHEK9231 / UNKLA / IMAdministered by: Senior Living Purchased by: ? Symptoms: Death, Dizziness, Unresponsive to stimuli, Vital functions abnormal SMQs:, Hyperglycaemia/new onset diabetes mellitus (broad), Neuroleptic malignant syndrome (broad), Anticholinergic syndrome (broad), Guillain-Barre syndrome (broad), Noninfectious encephalitis (broad), Noninfectious encephalopathy/delirium (broad), Noninfectious meningitis (broad), Vestibular disorders (broad), Hypotonic-hyporesponsive episode (broad), Hypoglycaemia (broad)Life Threatening? No Birth Defect? No Died? Yes Date died: 2021-01-13 Days after onset: 0 Permanent Disability? No Recovered? No Office Visit? No ER Visit? No ER or Doctor Visit? No Hospitalized? No Previous Vaccinations: Other Medications: unknown Current Illness: none Preexisting Conditions: yes Allergies: unknown Diagnostic Lab Data: CDC Split Type:Write-up: little bit of a reaction light headed after 5 minutes. vitals were low, so observed for 30 minutes after being light headed. Patient was found unresponsive and pronounced dead later that day. |
| VAERS ID:942072 (history) Form:Version 2.0 Age:87.0 Sex:Female Location:Vermont Vaccinated:2021-01-02Onset:2021-01-05 Days after vaccination:3Submitted:0000-00-00Entered:2021-01-13Vaccination / ManufacturerLot / DoseSite / RouteCOVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH- / 1- / IMAdministered by: Senior Living Purchased by: ? Symptoms: Aspiration, Death, Dementia, SARS-CoV-2 test negative SMQs:, Dementia (narrow), Noninfectious encephalopathy/delirium (broad), COVID-19 (broad)Life Threatening? No Birth Defect? No Died? Yes Date died: 2021-01-05 Days after onset: 0 Permanent Disability? No Recovered? No Office Visit? No ER Visit? No ER or Doctor Visit? No Hospitalized? No Previous Vaccinations: Other Medications: Tramadol, risperidone, fluoxetine, cyanocobalamin, colchicine, torsemide, levothyroxine Current Illness: aspiration pneumonia- completed treatment prior to vaccination. Preexisting Conditions: Advanced dementia with severe violent behavioral symptoms. Progressive decline and frailty due to late stage dementia with likely terminal aspiration after completion of treatment for previous aspiration pneumonia. Death attributed to complications of her advanced dementia. No evidence of acute reaction to vaccine (rash, dyspnea, swelling, redness). Chronic kidney disease, hypothyroidism, type 2 diabetes, gout, B12 deficiency Allergies: No known allergies Diagnostic Lab Data: COVID-19 PCR neg on 12/31/20 and 1/3/21 CDC Split Type:Write-up: Death occurred 3 days after vaccine receipt; attributed to complications of her chronic advanced dementia with aspiration at age 87. No evidence of acute vaccine reaction. |
| VAERS ID:942085 (history) Form:Version 2.0 Age:62.0 Sex:Female Location:Kansas Vaccinated:2021-01-02Onset:2021-01-08 Days after vaccination:6Submitted:0000-00-00Entered:2021-01-13Vaccination / ManufacturerLot / DoseSite / RouteCOVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECHFL0142 / 1LA / IMAdministered by: Senior Living Purchased by: ? Symptoms: Dyspnoea, Livedo reticularis, Pain, Pulse absent, Tremor, Unresponsive to stimuli SMQs:, Anaphylactic reaction (broad), Hyperglycaemia/new onset diabetes mellitus (broad), Neuroleptic malignant syndrome (broad), Shock-associated circulatory or cardiac conditions (excl torsade de pointes) (narrow), Parkinson-like events (broad), Acute central respiratory depression (broad), Pulmonary hypertension (broad), Guillain-Barre syndrome (broad), Noninfectious encephalitis (broad), Noninfectious encephalopathy/delirium (broad), Noninfectious meningitis (broad), Cardiomyopathy (broad), Hypotonic-hyporesponsive episode (broad), Hypoglycaemia (broad)Life Threatening? No Birth Defect? No Died? Yes Date died: 2021-01-08 Days after onset: 0 Permanent Disability? No Recovered? No Office Visit? No ER Visit? No ER or Doctor Visit? No Hospitalized? No Previous Vaccinations: Other Medications: Ativen, Butrans Patch, Tylenol, Potassium Citrate-Citric Acid Current Illness: Medical diagnosis: quadriplegia, Atherosclerotic heart disease Preexisting Conditions: see #11. Allergies: Amoxicillin, Clavulanic Acid, Codeine, Morphine, Pencillin Diagnostic Lab Data: CDC Split Type:Write-up: No adverse effects from vaccination seen on 1/2/21. On 1/6/21 resident was seen by Dr and her baclofen pump was refilled with 20 ml Baclofen 4,000mcg/ml. ITB Rate increased by 6% to 455.5 mcg/day simple continuous rate over 3 days. On 1/8/21 at 0615 resident was shaking, lower extremities mottled, Sa02 70%, pulse 45. Oxygen started at 2 L/m per NC. At 0715 her primary physician was notified as well as her daughter. Oxygen increased to 4 L/min, sats at 83%. SOA noted, reported all over pain. At 0850 when they attempted to reposition the resident, she was not responsive. Licensed nurse assessed her and no heartbeat heard or pulse found. |
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