CDC to Roll out Cell Phone-Based Surveillance System for Monitoring COVID-19 Vaccine Recipients
|
By HospiMedica International staff writers Posted on 26 Oct 2020 |

Illustration
The US Centers for Disease Control and Prevention (CDC Atlanta, GA, USA) has added a new safety monitoring system to evaluate the safety of COVID-19 vaccines in real time and ensure that they are as safe as possible after they are authorized or approved for use.
Currently, clinical trials are evaluating investigational COVID-19 vaccines in many thousands of study participants to generate scientific data and other information for the Food and Drug Administration (FDA) to determine their safety and effectiveness. After a vaccine is authorized or approved for use, many vaccine safety monitoring systems watch for adverse events (possible side effects). This continued monitoring can pick up on adverse events that may not have been seen in clinical trials. If an unexpected adverse event is seen, experts quickly study it further to assess whether it is a true safety concern. Experts then decide whether changes are needed in vaccine recommendations. This monitoring is critical to help ensure that the benefits continue to outweigh the risks for people who receive vaccines.
As people get vaccinated, CDC, FDA, and other federal partners will use robust systems and data sources to conduct ongoing safety monitoring. Among its various safety monitoring systems, the CDC plans to use a new smartphone-based, after-vaccination health checker named V-SAFE for people who receive COVID-19 vaccines. V-SAFE is a smartphone-based text, text-to-web survey, and email-to-web survey active surveillance program for early vaccine recipients. V-SAFE uses contact information (phone numbers) from the registration process for COVID-19 vaccination of essential workers - up to 20+ million people during the first few months of a vaccination program.
V-SAFE will use text messaging and web surveys from CDC to check in with vaccine recipients for health problems following COVID-19 vaccination. V-SAFE will conduct health checks on vaccine recipients via text messages and email daily for the first week post-vaccination and weekly thereafter for six weeks post-vaccination. The system also will provide telephone follow up to anyone who reports medically significant (important) adverse events.
Related Links:
Centers for Disease Control and Prevention (CDC)
Currently, clinical trials are evaluating investigational COVID-19 vaccines in many thousands of study participants to generate scientific data and other information for the Food and Drug Administration (FDA) to determine their safety and effectiveness. After a vaccine is authorized or approved for use, many vaccine safety monitoring systems watch for adverse events (possible side effects). This continued monitoring can pick up on adverse events that may not have been seen in clinical trials. If an unexpected adverse event is seen, experts quickly study it further to assess whether it is a true safety concern. Experts then decide whether changes are needed in vaccine recommendations. This monitoring is critical to help ensure that the benefits continue to outweigh the risks for people who receive vaccines.
As people get vaccinated, CDC, FDA, and other federal partners will use robust systems and data sources to conduct ongoing safety monitoring. Among its various safety monitoring systems, the CDC plans to use a new smartphone-based, after-vaccination health checker named V-SAFE for people who receive COVID-19 vaccines. V-SAFE is a smartphone-based text, text-to-web survey, and email-to-web survey active surveillance program for early vaccine recipients. V-SAFE uses contact information (phone numbers) from the registration process for COVID-19 vaccination of essential workers - up to 20+ million people during the first few months of a vaccination program.
V-SAFE will use text messaging and web surveys from CDC to check in with vaccine recipients for health problems following COVID-19 vaccination. V-SAFE will conduct health checks on vaccine recipients via text messages and email daily for the first week post-vaccination and weekly thereafter for six weeks post-vaccination. The system also will provide telephone follow up to anyone who reports medically significant (important) adverse events.
Related Links:
Centers for Disease Control and Prevention (CDC)
Latest COVID-19 News
- Low-Cost System Detects SARS-CoV-2 Virus in Hospital Air Using High-Tech Bubbles
- World's First Inhalable COVID-19 Vaccine Approved in China
- COVID-19 Vaccine Patch Fights SARS-CoV-2 Variants Better than Needles
- Blood Viscosity Testing Can Predict Risk of Death in Hospitalized COVID-19 Patients
- ‘Covid Computer’ Uses AI to Detect COVID-19 from Chest CT Scans
- MRI Lung-Imaging Technique Shows Cause of Long-COVID Symptoms
- Chest CT Scans of COVID-19 Patients Could Help Distinguish Between SARS-CoV-2 Variants
- Specialized MRI Detects Lung Abnormalities in Non-Hospitalized Long COVID Patients
- AI Algorithm Identifies Hospitalized Patients at Highest Risk of Dying From COVID-19
- Sweat Sensor Detects Key Biomarkers That Provide Early Warning of COVID-19 and Flu
- Study Assesses Impact of COVID-19 on Ventilation/Perfusion Scintigraphy
- CT Imaging Study Finds Vaccination Reduces Risk of COVID-19 Associated Pulmonary Embolism
- Third Day in Hospital a ‘Tipping Point’ in Severity of COVID-19 Pneumonia
- Longer Interval Between COVID-19 Vaccines Generates Up to Nine Times as Many Antibodies
- AI Model for Monitoring COVID-19 Predicts Mortality Within First 30 Days of Admission
- AI Predicts COVID Prognosis at Near-Expert Level Based Off CT Scans
Channels
Artificial Intelligence
view channelAI Improves Non-Contrast CT Interpretation for Time-Sensitive Stroke Assessment
Acute ischemic stroke occurs when a blood vessel in the brain becomes blocked, requiring rapid diagnosis to enable timely reperfusion therapy. Emergency departments often use computed tomography angiography... Read more
AI-Powered ECG Model Gains FDA Authorization for Emergency Cardiac Assessment
Powerful Medical’s PMcardio Queen of Hearts (ACS AI ECG Model) has received U.S. Food and Drug Administration (FDA) De Novo authorization, announced on September 15, 2026. The model is designed to identify... Read moreCritical Care
view channel
Portable Artificial Lung Technology Could Reshape Care for Chronic Lung Disease
Chronic lung disease can leave patients dependent on prolonged mechanical ventilation or awaiting transplantation, both of which carry substantial morbidity and healthcare costs. Ventilatory support may... Read more
Multimodal AI Improves Treatment Response Prediction in Lung Cancer
Immunotherapy has transformed care for advanced non-small cell lung cancer (NSCLC), yet only a minority of patients achieve durable benefit. Clinicians still struggle to predict who will respond, and treatment... Read more
New Approach Helps Identify Materials for More Reliable Wearable Electronics
Wearable health monitors and electronic skin must maintain stable performance while being stretched and bent. Molecular single crystals are promising for such stretchable electronics, yet the microscale... Read more
Scotland Adopts Respiratory Infection Control Guidance Informed by Aerosol Research
Preventing respiratory infection transmission in hospitals remains a core patient and staff safety priority. Many precautions have hinged on the assumption that certain clinical interventions create high-risk... Read moreSurgical Techniques
view channel
Robotic Platform Advances Fetoscopic Treatment of Twin-to-Twin Transfusion Syndrome
Twin-to-twin transfusion syndrome is a life-threatening complication in monochorionic twin pregnancies caused by unbalanced placental blood flow. Definitive treatment requires endoscopic laser coagulation... Read more
Patient-Specific AI Tool Aligns X-Rays With 3D Scans For Surgical Navigation
Minimally invasive procedures rely on real-time X-rays for navigation, but two-dimensional images can obscure the precise location and orientation of instruments inside the body. This uncertainty can prolong... Read more
Hydrogel Dermal Supports Healing of Complex Wounds After Cancer Surgery
Full-thickness skin defects following cancer excision challenge reconstructive teams because grafts and flaps can add donor-site morbidity and prolong recovery. These wounds are common on cosmetically... Read more
FDA Clears Integrated Platform for Real-Time Cardiac Imaging and Catheter Guidance
Catheter-based treatment of cardiac arrhythmias relies on precise, real-time visualization and navigation for safe, accurate therapy delivery. Yet electrophysiology teams often use separate imaging, mapping,... Read morePatient Care
view channel
EHR Model Flags High-Risk Periods in Patients with Metastatic Breast Cancer
Determining when patients with metastatic breast cancer are nearing the end of life remains difficult, often leading to intensive interventions with limited benefit. Prognostic uncertainty can delay goals-of-care... Read more
Virtual Reality Helps Claustrophobic Patients Complete Cardiac PET/CT Scans
Anxiety and claustrophobia—intense fear of confined spaces—often prevent patients from completing cardiac positron emission tomography/computed tomography (PET/CT). Aborted scans delay diagnosis, consume... Read moreMedical Imaging
view channel
Structure-Aware AI Aims to Improve Reliability of Medical Image Analysis
Clinicians increasingly rely on medical imaging to guide diagnosis and treatment, but machine learning systems used to analyze these images can be unreliable and difficult to interpret. Small, heterogeneous... Read more
PSMA PET/CT Helps Guide Pre-Biopsy Decisions in Prostate Cancer
Prostate cancer evaluation often begins with prostate-specific antigen (PSA) testing, but elevated levels are not specific to cancer and can lead to unnecessary biopsies. These procedures carry risks of... Read more
AI Models Evaluated for Spotting Ischemic Stroke Lesions on Routine MRI
Rapid detection of ischemic stroke on brain MRI is essential because treatment benefit declines with time. Many centers first acquire contrast-free MRI FLAIR sequences because they are quick and broadly... Read more
Noninvasive MRI Spectroscopy Classifies Pediatric Medulloblastoma Molecular Subgroups
Medulloblastoma, the most common malignant pediatric brain tumor, requires precise molecular classification to guide therapy and predict outcomes. Current subgrouping typically depends on surgical sampling... Read moreHealth IT
view channel
New Tablet Platform Extends Stroke Neurorehabilitation Beyond the Clinic
Continuity and intensity of neurorehabilitation after stroke are critical for functional recovery, but access to ongoing therapy at home often remains limited. Hospitals and outpatient programs therefore... Read more
Smartphone App Improves Blood Pressure Control in Hypertension
Hypertension, or high blood pressure, is a major modifiable driver of cardiovascular, renal, and cerebrovascular morbidity. Despite effective therapies, many adults fail to achieve control, leading to... Read morePoint of Care
view channel
Microneedle Patch Enables At-Home Monitoring of Acute Kidney Injury
Kidney disease is often silent in its early stages, making timely detection difficult outside clinical settings. Early biomarkers such as neutrophil gelatinase–associated lipocalin can require blood draws... Read more
Ultrathin Metasurface Could Bring Quantitative Phase Imaging to Portable Devices
Point-of-care imaging often depends on bulky optical systems that have difficulty visualizing nearly transparent cells and tissues without staining. These limitations can slow diagnosis and restrict use... Read moreBusiness
view channel
Medtronic Receives FDA Clearance for Vessel-Sealing Instrument for Robotic Surgery
As robotic-assisted surgery expands across U.S. hospitals, teams increasingly seek energy instruments with the familiarity and performance of tools used in open and laparoscopic procedures.... Read more
Robotic Single-Port System Gains CE Mark for Transvaginal Gynecologic Procedures
Intuitive (Sunnyvale, CA, USA) announced that it has received CE mark approval for use of the da Vinci SP Single Port surgical system in transvaginal gynecologic procedures, marking the first such indication... Read more








