Pharmaceutical
Detect more adverse events with less PV effort
Datashake powers healthcare and pharmaceutical intelligence with real-time access to patient, product, and market data from public sources. Detect adverse events, map patient journeys, and understand treatment perceptions with untapped compliant data.
Trusted by global companies
150
+
sources and counting
98.3
%
uptime SLA
5
+
years of historical data
What Pharmaceutical platforms build with Datashake
Adverse event signal detection
Competitor & market intelligence
Patient journey mapping
Treatment perception & sentiment analysis
Pharmacovigilance automation
KOL & congress monitoring
App & device feedback analysis
Disease community intelligence
Power pharmacovigilance with the most complete data
Datashake consolidates patient discussions from 150+ sources into structured, medically-enriched datasets. Automatically feed your PV systems with safety signals that are compliant and ready for medical review.
Stop missing adverse events because monitoring is manual. Stop wasting PV resources on unstructured social posts. Stop limiting coverage because of compliance concerns. Datashake delivers automated, healthcare-aware, audit-ready data that makes safety surveillance comprehensive and defensible.
Eliminate manual screening burden
Pull patient safety discussions from social media, forums, app reviews, and patient communities into pre-enriched, PV-ready datasets. Configure monitoring once, adverse event signals surface automatically, and PV teams review structured findings instead of interpreting raw social posts.
Detect safety signals before they escalate
Real-time monitoring delivers patient-reported adverse events rapidly, enabling quick response. Catch emerging side effects, quality issues, and sentiment shifts while response options are still open.
Feed compliant data into PV workflows with confidence
Structured JSON integrates with pharmacovigilance case management systems. 100% pre-login public data with complete audit trails powers safety decisions without compliance exposure or patient privacy risk.
Scale pharmacovigilance across therapeutic areas and markets
Expand safety monitoring effortlessly
Add new therapeutic areas, products, or patient communities without engineering work or system changes. Your surveillance coverage expands seamlessly as your portfolio and regulatory requirements grow.
Support global operations from one system
Multi-language, multi-region patient data collection powers multinational pharmaceutical operations. Monitor safety signals across any geography without deploying regional infrastructure or managing fragmented vendors.
Maintain PV productivity at any scale
Data quality and structure stay consistent whether monitoring one product or an entire portfolio. PV teams use the same workflows regardless of therapeutic area scope, without performance degradation as surveillance programs expand.
Adapt monitoring to safety urgency
Real-time alerts for urgent adverse events. Daily surveillance for routine monitoring. Historical access for baseline analysis and trend detection. Flexible delivery matches data cadence to signal urgency and regulatory requirements.
Review Management Services
I’ve been using Datashake for over six years, and it’s been a big part of our business growth during that time. It has really helped improve our operations by providing consistent, reliable data that we can easily plug into our workflows.
Tech Lead
Review Management Services
Partnering with Datashake has been a great experience. Their customer success team is responsive, knowledgeable, and always quick to help. They’re open to evolving the product as our needs grow, and their framework makes scaling up or down extremely easy.
Senior Technical Partner Manager
Review Management Services
I’ve been using Datashake for over six years, and it’s been a big part of our business growth during that time. It has really helped improve our operations by providing consistent, reliable data that we can easily plug into our workflows.
Founder & Product Lead
How Datashake powers pharmaceutical intelligence
Accelerate case review with clean, contextualized signals
Eliminate noise through high deduplication accuracy. Surface complete conversation threads revealing full patient context. Leverage rich metadata to prioritize and validate signals. Integrate seamlessly with PV systems through standard JSON.
Detect emerging risks while tracking long-term patterns
Catch adverse events as they surface with real-time monitoring. Query historical data to establish baselines and identify trends. Switch between urgent surveillance and strategic analysis instantly – one system handles both.
Plug into workflows and empower teams
Connect APIs directly to case management systems and safety databases. Enable specialists and medical reviewers to explore signals independently through Datashake Hub. Execute flexible queries supporting daily screening and comprehensive investigations.
Launch comprehensive coverage in weeks
Step 01
POC with full access
Get complete API access to all 150+ sources. Test real queries with real data. Our team helps validate coverage, performance, and fit for your use cases.
Step 02
Define your solution
Configure source priorities, delivery methods, update frequencies, and pricing that supports your margins as you scale customers.
Step 03
Seamless onboarding
Dedicated technical support guides your integration. API optimization, workflow setup, and go-live validation so that you can get reliable performance from day one.
Customer Success
Put Datashake to the test for free
In a short benchmark trial, we’ll use your own search parameters to show how Datashake uncovers all the data points your current tools miss across social media, review sites, and niche sources.
Free, no-commitment benchmark test
Use your existing queries or filters
Compare results side-by-side
See how much more you could be capturing
FAQs
Your questions,
answered
How does Datashake detect adverse events from public sources?
We consolidate patient discussions from 150+ sources including social media, forums, app reviews, and patient communities into structured, PV-ready datasets. Adverse event signals surface automatically for medical review, eliminating manual screening burden while catching safety signals before they escalate.
Is Datashake data compliant for pharmacovigilance use?
Yes. We collect 100% pre-login public data with complete audit trails meeting regulatory requirements. Our healthcare-aware approach eliminates compliance exposure and patient privacy risk while powering safety decisions with defensible, audit-ready data.
How does Datashake integrate with existing PV systems?
Structured JSON feeds directly into pharmacovigilance case management systems through standard APIs. Data arrives pre-enriched and PV-ready so teams review structured findings instead of interpreting raw social posts.
Can we monitor patient discussions globally across regions?
Yes. Multi-language, multi-region patient data collection powers multinational pharmaceutical operations. Monitor safety signals across any geography without deploying regional infrastructure or managing fragmented vendors.
What types of patient data does Datashake capture?
We capture complete conversation threads revealing full patient context including treatment experiences, side effects, sentiment patterns, and product feedback. Rich metadata enables prioritization and validation of safety signals for comprehensive surveillance.
Can non-technical PV teams access and explore data?
Yes. APIs connect directly to case management systems for automated workflows, while Datashake Hub enables medical reviewers and specialists to explore signals independently without technical backgrounds for flexible investigations.
How does data quality stay consistent as monitoring expands?
Data quality and structure remain consistent whether monitoring one product or an entire portfolio. PV teams use the same workflows regardless of therapeutic area scope with no performance degradation.