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Naftidrofuryl Side Effects

Report Naftidrofuryl Side Effects

If you experienced any harmful or unwanted effects of Naftidrofuryl, please share your experience. This could help to raise awareness about Naftidrofuryl side effects, identify uknown risks and inform health professionals and patients taking Naftidrofuryl.

Examples: headache, dizziness


The most commonly reported Naftidrofuryl side effects are:
Hepatitis (1 reports)
Itching All Over Body (1 reports)

If you have experienced a side effect listed above, you can check a box to report it.


To view a complete list of submitted side effects, please follow the link Naftidrofuryl side effects . You can also compare Naftidrofuryl side effects or view FDA reports.

Naftidrofuryl Side Effects reported to FDA

The following Naftidrofuryl reports list potential signals of serious risks and new safety information that were identified using the FDA Adverse Event Reporting System (FAERS).
The FAERS is a database that contains information on adverse event and medication errors reports submitted to FDA by healthcare professionals (such as physicians, pharmacists, nurses and others), consumers (such as patients, family members, layers and others) and manufacturers.


The appearance of Naftidrofuryl on this list does not mean that FDA has concluded that the drug has the listed risk. It means that FDA has identified a potential safety issue, but it does not mean that FDA has identified a causal relationship between the drug and the listed risk.

Abdominal Pain Upper, Oesophageal Ulcer, Chest Pain
on Nov 16, 2011 Female from ITALY , 83 years of age, was treated with Naftidrofuryl (naftidrofuryl). Directly after, patient experienced the unwanted or unexpected Naftidrofuryl side effects: abdominal pain upper, oesophageal ulcer, chest pain. Naftidrofuryl (naftidrofuryl) dosage: (200), Oral Since Long Time -.
Associated medications used:
  • Pravastatin ((20 ), Oral Since Long Time -)
  • Aspirin
  • Furosemide ((20 ), Oral Since Long Time -)
  • Novomix (biphasic Insulin Aspart) (biphasic Insulin Aspart)
  • Nebivolol Hcl (Oral Since Long Time -)
  • Trimetazidine (trimetazidine) ((20 ), Oral Since Long Time -)
Patient was hospitalized.

Arthralgia, Vomiting, Rhabdomyolysis, Blood Creatine Phosphokinase Increased, Blood Urea Increased, Malaise, Chromaturia, Musculoskeletal Pain
Patient was taking Naftidrofuryl Oxalate. Patient felt the following Naftidrofuryl side effects: arthralgia, vomiting, rhabdomyolysis, blood creatine phosphokinase increased, blood urea increased, malaise, chromaturia, musculoskeletal pain on Aug 04, 2011 from Additional patient health information: Male , 57 years of age, . Naftidrofuryl Oxalate dosage: N/A.
Multiple prescriptions taken:
  • Trimethoprim (200 Mg (200 Mg,1 In 1 D), Oral)
  • Amlodipine
  • Aspirin
  • Simvastatin (40 Mg (40 Mg,1 In 1 D),oral)
  • Ranolazine (750 Mg (375 Mg,2 In 1 D), Oral : 1000 Mg (500 Mg,2 In 1 D),oral)
  • Ranolazine (750 Mg (375 Mg,2 In 1 D), Oral : 1000 Mg (500 Mg,2 In 1 D),oral)
  • Nitroglycerin
  • Carvedilol
Patient was hospitalized.

Rhabdomyolysis, Malaise
Adverse event was reported on Aug 05, 2011 by a Male taking Naftidrofuryl Oxalate (Dosage: N/A) . Location: UNITED KINGDOM , 57 years of age, After Naftidrofuryl was administered, patient encountered several Naftidrofuryl side effects: rhabdomyolysis, malaise.
Multiple concurrent drugs taken:
  • Amlodipine
  • Nicorandil
  • Trimethoprim (200 Mg (200 Mg,unk),oral)
  • Nitroglycerin
  • Isosorbide Mononitrate
  • Simvastatin (40 Mg (40 Mg, Unk),oral)
  • Carvedilol
  • Ramipril
Patient was hospitalized.

Rhabdomyolysis, Blood Urea Increased, Angina Pectoris, Vomiting, Chromaturia, Urinary Tract Infection
on Aug 04, 2011 Male from , 57 years of age, was treated with Naftidrofuryl Oxalate (naftidrofuryl Oxalate). Directly after, patient experienced the unwanted or unexpected Naftidrofuryl side effects: rhabdomyolysis, blood urea increased, angina pectoris, vomiting, chromaturia, urinary tract infection. Naftidrofuryl Oxalate (naftidrofuryl Oxalate) dosage: N/A.
Associated medications used:
  • Enoxaparin Sodium
  • Aspirin
  • Nitroglycerin
  • Ramipril
  • Simvastatin (40 Mg (40 Mg, 1 In 1 D),oral)
  • Carvedilol
  • Acetaminophen
  • Trimethoprim (200 Mg (200 Mg, 1 In 1 D),oral)
Patient was hospitalized.


Musculoskeletal Pain, Rhabdomyolysis, Urinary Tract Infection, Chromaturia, Malaise, Angina Pectoris, Vomiting, Arthralgia
on Aug 02, 2011 Male from , 57 years of age, was treated with Naftidrofuryl Oxalate (naftidrofuryl Oxalate). Patient felt the following Naftidrofuryl side effects: musculoskeletal pain, rhabdomyolysis, urinary tract infection, chromaturia, malaise, angina pectoris, vomiting, arthralgia. Naftidrofuryl Oxalate (naftidrofuryl Oxalate) dosage: N/A.
Multiple prescriptions taken: Patient was hospitalized.

Haemorrhagic Stroke, Lung Infection
Patient was taking Naftidrofuryl. After Naftidrofuryl was administered, patient encountered several Naftidrofuryl side effects: haemorrhagic stroke, lung infection on Jul 22, 2011 from FRANCE Additional patient health information: Male , 84 years of age, was diagnosed with
  • arterial disorder
  • hypertension
  • pain
  • depression
  • thrombosis prophylaxis
  • hypercholesterolaemia
and. Naftidrofuryl dosage: Unk.
Multiple concurrent drugs taken:
  • Micardis Hct (1 Df, 1x/day)
  • Acetaminophen (Unk)
  • Effexor Xr (75 Mg, 1x/day)
  • Plavix (Unk)
  • Crestor (10 Mg, 1x/day)
Patient was hospitalized.

Blood Creatine Phosphokinase Increased, Rhabdomyolysis
Adverse event was reported on Jun 17, 2011 by a Male taking Naftidrofuryl (Dosage: 300 Mg, Unk) . Location: UNITED KINGDOM , 57 years of age, Directly after, patient experienced the unwanted or unexpected Naftidrofuryl side effects: blood creatine phosphokinase increased, rhabdomyolysis.
Associated medications used:
  • Ramipril (5 Mg, Unk)
  • Isosorbide Mononitrate (120 Mg, Unk)
  • Ranexa (Unk)
  • Aspirin (75 Mg, Unk)
  • Nitroglycerin
  • Nicorandil (60 Mg, Unk)
  • Simvastatin (40 Mg, Unk)
  • Amlodipine (10 Mg, Unk)
Patient was hospitalized.

Record and Track Your Side Effects

It is very important to keep track of all side effects and discuss them with your doctor. If you think you may have a medical emergency, call your doctor or 911 immediately.

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Most drugs have a large list of nonsevere or mild adverse effects which do not rule out continued usage. These effects depend on individual sensitivity, and can include nausea, dizziness, diarrhea, malaise, vomiting, headache, dermatitis, dry mouth, etc. Check commonly reported side effects . These can be considered a form of pseudo-allergic reaction, as not all users experience these effects; many users experience none at all.

You are encouraged to report negative side effects of prescription drugs to the FDA. Visit the FDA MedWatch website or call 1-800-FDA-1088.

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Safety Alerts, Active Ingredients, Usage Information

More About Naftidrofuryl

Side Effects reported to FDA: 7

Naftidrofuryl safety alerts: No

Reported hospitalizations: 2

Latest Naftidrofuryl clinical trials

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