Product name as reported
Previscan: adverse event reports filed with FDA
4,106 reports list it as a suspect or interacting product, 2004–2021. Also reported as Previscan /00789001/, Previscan /00261401/.
- 4,106
- reports as suspect product
- 0% of all reports · about 183 a year
- 0
- reports, 12 months to June 2026
- 0 in the 12 months before
- 99.9%
- marked serious by the reporter
- 57.4% across all reports
- 17%
- record death among outcomes, as reported
- 696 reports · not verified by FDA
4,106 adverse event reports received by FDA list the product name "Previscan" as reporters wrote it as a suspect or interacting product, from January 2004 to September 2021. A further 6,116 reports list it only as a concomitant medication, and those are not counted in the figures on this page.
In the 12 months to June 2026, 0 reports listed it, and none in the 12 months before. FDA releases FAERS data quarterly, so the newest months are incomplete and grow in later releases. Over its reporting history that is about 183 reports a year and 0% of the 20,646,523 reports in the database. How many people take it is not in the data, so a count is not a rate of occurrence.
The MedDRA terms listed most often are international normalised ratio increased (26.9%), drug interaction (21.7%) and anaemia (12.5%). A report can list several reactions, so shares add to more than 100%; 640 different terms appear across these reports. International normalised ratio increased is recorded in 26.9% of these reports, against 0.1% of all reports in the database.
99.9% of the reports are marked serious by the reporter; 17% record death among the outcomes and 77.5% record hospitalisation, as reported. 48.4% of the reports came from other health professionals, and the largest patient age group is 75 and over (50.6%). FDA states that "a causal relationship cannot be established between product and reactions listed in a report" and that for any given report "there is no certainty that a suspected drug caused the event."
Reports by month, five years
Reports by the month FDA received them. FDA releases FAERS data quarterly, so the newest months are incomplete and grow in later releases.
By year received
Reactions recorded in the reports
share of Previscan reports recording the termall reports in the database
- International normalised ratio increasedblood clotting slower than intended (raised INR)26.9%1,106
- Drug interactionan interaction between medicines21.7%893
- Anaemialow red blood cells12.5%514
- Haematomaa collection of blood under the skin or in tissue8%330
- Overdosea dose above the recommended amount5.6%229
- Melaenablack tarry stools4.9%202
- Acute kidney injurysudden loss of kidney function4.7%194
- Rectal haemorrhage4.2%174
- Renal failurekidney failure4.1%168
- Falla fall3.9%161
- Subdural haematoma3.9%161
- Renal failure acute3.6%149
- Shock haemorrhagic3.4%141
- Muscle haemorrhage3.4%139
- Hyperkalaemiahigh blood potassium3.3%135
- Haematuriablood in the urine3%124
- Cerebral haematoma2.8%114
- Epistaxisnosebleed2.2%92
- Cerebral haemorrhage2.2%91
- Haemoglobin decreasedlow haemoglobin2.2%91
- Gastrointestinal haemorrhagebleeding in the stomach or bowel2.2%90
- Diarrhoealoose or frequent stools2.2%89
- Hypotensionlow blood pressure2.1%85
- Pyrexiafever2%84
- Interstitial lung diseasescarring or inflammation of lung tissue2%81
- Confusional stateconfusion1.9%79
- Dyspnoeashortness of breath1.9%79
- Thrombocytopenialow platelets1.9%79
- Eosinophilia1.9%78
- Vomitingbeing sick1.9%78
Top 30 of 640 MedDRA preferred terms recorded across these reports, with a plain-language gloss where one is available. One report can record several terms. The hollow bar is the share of all reports in the database; it describes the reports, not the patients. FDA states that adverse event reports "represent a small percentage of total usage numbers of a product", that "common products may have a higher number of adverse events due to the higher total number of people using the product", and that the data "by themselves are not an indicator of the safety profile of the drug or biologic."
Outcomes recorded
Outcome flags as the reporter set them; a report can carry several, and "other serious" is FDA's own category for serious reports outside the named outcomes. Grey bar: all 20,646,523 reports. FDA has not verified any outcome and states that the reports "cannot be used to estimate the incidence of these events."
Patients and reporters
Patient age
Patient sex
Who reported
Age and sex as stated in the report; the reporter's qualification is the primary source recorded by FDA. 0.3% of reports give the United States as the country of the event or reporter.
Reason for use recorded
| Indication as recorded (MedDRA) | Reports | Share |
|---|---|---|
| Atrial fibrillation | 1,016 | 24.7% |
| Thrombosis prophylaxis | 173 | 4.2% |
| Pulmonary embolism | 172 | 4.2% |
| Deep vein thrombosis | 94 | 2.3% |
| Arrhythmia | 71 | 1.7% |
| Prophylaxis | 58 | 1.4% |
The indication field is filled in by the reporter and is often blank; shares are of all 4,106 reports.
In context
| Measure | Previscan | All reports |
|---|---|---|
| Reports as suspect product | 4,106 | 20,646,523 |
| Share of that pool | — | 0% |
| Reports, latest 12 months | 0 | 1,332,454 |
| Marked serious | 99.9% | 57.4% |
| Death recorded among outcomes, per 1,000 reports | 170 | 91 |
| Hospitalisation recorded, per 1,000 reports | 775 | 213 |
| Consumer-filed share | 13.4% | 45.8% |
| Top term, share of reports | International normalised ratio increased 26.9% | 0.1% |
Shares are of reports, not of patients treated. The number of people taking a product is not in the data, so none of these figures is a rate, and differences between columns reflect who takes a product, who reports and how long it has been sold. FDA states that adverse event reports "represent a small percentage of total usage numbers of a product", that "common products may have a higher number of adverse events due to the higher total number of people using the product", and that the data "by themselves are not an indicator of the safety profile of the drug or biologic."
Questions about Previscan reports
How many adverse event reports has FDA received for Previscan?
4,106 reports list Previscan as a suspect or interacting product in the openFDA FAERS release of 28 Sep 2026, covering reports received through June 2026. 0 of them arrived in the latest 12 months. Another 6,116 list it only as a concomitant medication.
What reactions are recorded in Previscan reports?
international normalised ratio increased (26.9%), drug interaction (21.7%), anaemia (12.5%), haematoma (8%) and overdose (5.6%). These are MedDRA preferred terms coded from what the reporter described; a report can list several, and a term's presence is not a finding that Previscan was responsible.
How serious are the reports?
99.9% are marked serious by the reporter. Among the outcomes recorded, 17% of reports include death and 77.5% include hospitalisation. FDA has not verified these outcomes and states that the reports "cannot be used to estimate the incidence" of the events.
Who files these reports?
other health professional (48.4%), physician (24.4%) and consumer or non-health professional (13.4%). Most reports reach FDA through the manufacturer, which must forward reports it receives.
Are reports for Previscan rising?
0 reports in the 12 months to June 2026, and none in the 12 months before. FDA releases FAERS data quarterly, so the newest months are incomplete and grow in later releases. Counts also move with how many people take a product, its time on the market and publicity.
Do these reports show that Previscan was responsible for these reactions?
No. FDA states that "a causal relationship cannot be established between product and reactions listed in a report" and that for any given report "there is no certainty that a suspected drug caused the event." The reaction may relate to the condition being treated, to other medicines, or to something else.
Is this a list of the side effects of Previscan?
No. It is a count of what was reported to FDA. The adverse reactions observed in clinical studies are printed on the FDA-approved label, which a pharmacist or clinician can go through with you.
How do I report an adverse event?
Consumers and health professionals can report to FDA through MedWatch (Form FDA 3500 online, or 1-800-FDA-1088), or to the manufacturer, which must pass reports on. See the guide on how to report.
Where this comes from. Counts are built from the openFDA Drug Adverse Event (FAERS) bulk export released 28 Sep 2026, which holds reports FDA received through 30 Jun 2026. Drug names are as reported, resolved to the brand or generic name on the FDA label where openFDA's harmonisation matched them; classes are the pharmacologic class (EPC) from the label and the National Drug Code Directory of 17 Sep 2026. A report counts here when it lists Previscan as a suspect or interacting product; reports listing it only as a concomitant medication (6,116) are excluded. No report narrative, lot number, patient detail or reporter identity is published. See the methodology and sources; FDA's record is authoritative, and corrections are handled within five working days.
Drug data (FAERS) through 30 Jun 2026; device data (MAUDE) through 31 Aug 2026. Not medical advice.