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Anaphylaxis!!! Thank goodness an emergency room was in the building. I have never had ...Keep Reading

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Sotradecol adverse events reported to FDA.

Have You Experienced unusual Sotradecol symptoms? PatientsVille.com collects and analyzes Sotradecol side effect and adverse reports submitted by Sotradecol users, such as .

Summary

FDA Adverse Reports: 19. View All

Sotradecol FDA safety alerts: No

Reported hospitalizations: 7

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Often additional risks of using a medication, such as Sotradecol, become known after product is used by a larger number of patients, for a longer period of time, and by patients with different health characteristics from those studied before drug approval. This page allows You to Find answers and discuss health symptoms with other Sotradecol users, Learn more about unwanted side effects & find ways to reduce them. Browse Sotradecol Adverse Reports reported to FDA and participate in Sotradecol discussion, find alternative treatments and find ways to avoid or reduce risks associated with using Sotradecol. You can also Post a question to users community or Ask a Doctor. PatientsVille.com is Your Complete Guide to all common, undocumented and undisclosed side effects associated with drugs and vaccines. Browse More Drug Reports Here: A  B  C  D  E  F  G  H  I  J  K  L  M  N  O  P  Q  R  S  T  U  V  W  X  Y  Z

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Sotradecol Adverse Effect Reports (FDA)

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6535842-X | Air Embolism, Aphasia, Cerebral Artery Embolism, Fall, Hemiparesis, Muscular Weakness, Nih Stroke Scale Score Increased, Procedural Complication, Sensory Loss
on Dec 21, 2009 Female patient from UNITED STATES , 38 years of age, was treated with Sotradecol (View Usage). Patient experienced the following unwanted or unexpected effects: air embolism, aphasia (What is aphasia?), cerebral artery embolism, fall (What is fall?), hemiparesis, muscular weakness, nih stroke scale score increased, procedural complication, sensory loss. Sotradecol dosage: Intravenous. Patient was hospitalized.

6304083-3 | Necrosis, Post Procedural Complication, Vein Disorder
Patient was taking Sotradecol (View Usage). Patient had the following side effects: necrosis, post procedural complication, vein disorder on Aug 10, 2009 from UNITED STATES Additional patient health information: Female patient , 54 years of age, was diagnosed with telangiectasia and. Sotradecol dosage: 0.5cc 1 Iv.

6282518-2 | Hyperhidrosis, Hypotension, Injection Site Irritation, Injection Site Pain, Loss Of Consciousness, Nausea, Road Traffic Accident, Skin Discolouration, Tinnitus
Adverse event was reported on Jul 22, 2009 by a Male patient taking Sotradecol (View Usage) (Dosage: ) was diagnosed with varicose vein operation and. Location: UNITED STATES , 40 years of age, weighting 240.0 lb, After Sotradecol was administered, patient had the following side effects: hyperhidrosis, hypotension, injection site irritation, injection site pain, loss of consciousness, nausea (What is nausea?), road traffic accident, skin discolouration, tinnitus (What is tinnitus?). Patient was hospitalized.

5796550-6 | Acne, Alopecia, Arthralgia, Fatigue, Pain In Extremity, Poisoning, Urticaria, Weight Bearing Difficulty
on Jun 30, 2008 Female patient from UNITED STATES , 56 years of age, weighting 130.0 lb, was diagnosed with spider vein and was treated with Sotradecol (View Usage). Patient experienced the following unwanted or unexpected effects: acne (What is acne?), alopecia, arthralgia, fatigue, pain in extremity, poisoning (What is poisoning?), urticaria, weight bearing difficulty. Sotradecol dosage: One Time Injection. During the same period patient was treated with GLYCERINE (One Time Injection) (View Glycerine Review and Glycerine Label ).


5608020-6 | Cardiac Arrest, Ear Discomfort, Eye Irritation, Hypertension, Loss Of Consciousness, Oral Discomfort, Procedural Complication, Shock, Tremor
on Jan 28, 2008 Female patient from UNITED STATES , 69 years of age, weighting 148.0 lb, was diagnosed with surgery (What is surgery?) and was treated with Sotradecol (View Usage). Patient had the following side effects: cardiac arrest (What is cardiac arrest?), ear discomfort, eye irritation, hypertension, loss of consciousness, oral discomfort, procedural complication, shock, tremor. Sotradecol dosage: .

5594664-7 | Hypersensitivity, Injection Site Extravasation, Serratia Infection, Skin Ulcer
Patient was taking Sotradecol (View Usage). After Sotradecol was administered, patient had the following side effects: hypersensitivity, injection site extravasation, serratia infection, skin ulcer on Aug 01, 2007 from UNITED STATES Additional patient health information: Female patient , 51 years of age, was diagnosed with spider vein and. Sotradecol dosage: Intravenous. During the same period patient was treated with CALCIUM (View Calcium Review and Calcium Label ), ASCORBIC ACID (View Ascorbic Acid Review and Ascorbic Acid Label ), BETA CAROTENE (View Beta-carotene Review and Beta-carotene Label ), MULTI VITAMIN (View Multi-vitamin Review and Multi-vitamin Label ), GLUCOSAMINE/CHONDROITIN (View Glucosamine/chondroitin Review and Glucosamine/chondroitin Label ), VITAMIN E (View Vitamin E Review and Vitamin E Label ), ACIDOPHILUS (View Acidophilus Review and Acidophilus Label ), HORSE CHESTNUT (FOR BACK) (View Horse Chestnut (for Back) Review and Horse Chestnut (for Back) Label ).

5460887-0 | Erythema, Eschar, Ulcer
Adverse event was reported on Jun 06, 2007 by a Female patient taking Sotradecol (View Usage) (Dosage: Once, Intravenous (not Specified)) was diagnosed with varicose vein (What is varicose vein?) and. Location: UNITED STATES , 47 years of age, Patient experienced the following unwanted or unexpected effects: erythema, eschar, ulcer (What is ulcer?).

5460886-9 | Erythema, Skin Exfoliation, Ulcer
on Jun 06, 2007 Female patient from UNITED STATES , 72 years of age, was diagnosed with spider vein, varicose vein (What is varicose vein?) and was treated with Sotradecol (View Usage). Patient had the following side effects: erythema, skin exfoliation, ulcer (What is ulcer?). Sotradecol dosage: Once, Intravenous (not Specified). During the same period patient was treated with ASPIRIN (View Aspirin Review and Aspirin Label ), LIPITOR (View Lipitor Review and Lipitor Label ), VALTREX (View Valtrex Review and Valtrex Label ).

5460885-7 | Erythema, Eschar, Ulcer
on Jun 06, 2007 Female patient from UNITED STATES , 33 years of age, was diagnosed with spider vein, varicose vein (What is varicose vein?) and was treated with Sotradecol (View Usage). After Sotradecol was administered, patient had the following side effects: erythema, eschar, ulcer (What is ulcer?). Sotradecol dosage: Once, Intravenous (not Specified).

5460884-5 | Erythema, Eschar, Ulcer
Patient was taking Sotradecol (View Usage). Patient experienced the following unwanted or unexpected effects: erythema, eschar, ulcer (What is ulcer?) on Jun 06, 2007 from UNITED STATES Additional patient health information: Female patient , 50 years of age, was diagnosed with spider vein and. Sotradecol dosage: Once, Intravenous (not Specified).

5460883-3 | Erythema, Eschar, Ulcer
Adverse event was reported on Jun 06, 2007 by a Female patient taking Sotradecol (View Usage) (Dosage: Twice, Intravenous (not Specified)) was diagnosed with spider vein and. Location: UNITED STATES , 44 years of age, Patient had the following side effects: erythema, eschar, ulcer (What is ulcer?).

5460882-1 | Ulcer
on Jun 06, 2007 Female patient from UNITED STATES , 60 years of age, was diagnosed with spider vein and was treated with Sotradecol (View Usage). After Sotradecol was administered, patient had the following side effects: ulcer (What is ulcer?). Sotradecol dosage: Once, Intravenous (not Specified). During the same period patient was treated with ACTONEL (View Actonel Review and Actonel Label ).

5460881-X | Erythema, Ulcer
on Jun 06, 2007 Female patient from UNITED STATES , 52 years of age, was diagnosed with spider vein and was treated with Sotradecol (View Usage). Patient experienced the following unwanted or unexpected effects: erythema, ulcer (What is ulcer?). Sotradecol dosage: Once, Intravenous (not Specified).

5320835-0 | Chromaturia, Diarrhoea, Renal Failure Acute
Patient was taking Sotradecol (View Usage). Patient had the following side effects: chromaturia, diarrhoea, renal failure acute on Oct 05, 2006 from UNITED STATES Additional patient health information: Male patient , child 10 years of age, was diagnosed with malformation venous and. Sotradecol dosage: 10cc, Single Dose, Iv. During the same period patient was treated with ETHIODOL (View Ethiodol Review and Ethiodol Label ). Patient was hospitalized.

5320833-7 | Anaphylactic Shock, Dysgeusia, Feeling Hot, Headache, Hypersensitivity, Immediate Post-injection Reaction, International Normalised Ratio Increased, Loss Of Consciousness, Oxygen Saturation Decreased
Adverse event was reported on Apr 11, 2007 by a Female patient taking Sotradecol (View Usage) (Dosage: 2 Ml Of 1% So;lution, Intravenous) . Location: UNITED STATES , weighting 149.9 lb, After Sotradecol was administered, patient had the following side effects: anaphylactic shock, dysgeusia, feeling hot, headache (What is headache?), hypersensitivity, immediate post-injection reaction, international normalised ratio increased, loss of consciousness, oxygen saturation decreased. During the same period patient was treated with COUMADIN (View Coumadin Review and Coumadin Label ), ACTONEL (View Actonel Review and Actonel Label ), CARDIZEM CD (View Cardizem Cd Review and Cardizem Cd Label ). Patient was hospitalized.

5314654-9 | Anaphylactic Shock, Dysgeusia, Headache, Hypersensitivity, Loss Of Consciousness, Oxygen Saturation Decreased
on Apr 11, 2007 Female patient from UNITED STATES , 69 years of age, weighting 149.9 lb, was treated with Sotradecol (View Usage). Patient experienced the following unwanted or unexpected effects: anaphylactic shock, dysgeusia, headache (What is headache?), hypersensitivity, loss of consciousness, oxygen saturation decreased. Sotradecol dosage: 2ml Of 1% Solution, Intravenous. During the same period patient was treated with COUMADIN (View Coumadin Review and Coumadin Label ), ACTONEL (View Actonel Review and Actonel Label ), CARDIZEM CD (View Cardizem Cd Review and Cardizem Cd Label ). Patient was hospitalized.

5290995-9 | Pulmonary Embolism
on Apr 05, 2007 Female patient from UNITED STATES , weighting 108.0 lb, was treated with Sotradecol (View Usage). Patient had the following side effects: pulmonary embolism (What is pulmonary embolism?). Sotradecol dosage: .

5278457-6 | Anaphylactic Shock, Dysgeusia, Headache, Hypersensitivity
Patient was taking Sotradecol (View Usage). After Sotradecol was administered, patient had the following side effects: anaphylactic shock, dysgeusia, headache (What is headache?), hypersensitivity on Mar 06, 2007 from UNITED STATES Additional patient health information: Female patient , 69 years of age, weighting 149.9 lb, . Sotradecol dosage: 2ml Of 1% Solution, Intravenous. During the same period patient was treated with COUMADIN (View Coumadin Review and Coumadin Label ), ACTONEL (View Actonel Review and Actonel Label ), CARDIZEM CD (View Cardizem Cd Review and Cardizem Cd Label ). Patient was hospitalized.

5136043-2 | Diarrhoea, Off Label Use, Renal Failure Acute
Adverse event was reported on Oct 05, 2006 by a Female patient taking Sotradecol (View Usage) (Dosage: 10cc, Single Dose, Iv) was diagnosed with malformation venous and. Location: UNITED STATES , child 10 years of age, Patient experienced the following unwanted or unexpected effects: diarrhoea, off label use, renal failure acute. During the same period patient was treated with ETHIODOL (View Ethiodol Review and Ethiodol Label ). Patient was hospitalized.


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To find out about documented side effects or safety concerns read either the drug label or the drug's package insert. You may also want to speak with your pharmacist or healthcare provider. All medicines have benefits and risks. The risks are the chances that something unwanted or unexpected could happen to you when you use them. You can protect yourself by searching summaries of recent safety alerts, adverse reports. Sometimes there are risks that only come to light after a medical product gets on the market and is used in a larger number of patients, for a longer period of time, and in patients whose health characteristics are different from those of the patients studied before approval.

Be aware of the following potential Sotradecol risks to be aware of: 1. Watch for any Serious adverse events, such as life-threatening situation, which can require an admission to hospital or longer-than-expected hospital stay, permanent disability, birth defect, miscarriage, stillbirth, or birth with serious disease requires medical care to prevent permanent damage
2. Any potential Sotradecol quality problem: suspected counterfeit product, potentially contaminated product indicated by suspicious odor or unusual color, inaccurate or unreadable product labeling
3. Potential Sotradecol use error: mixing up products with similar drug names or packaging, taking wrong dose of a drug because of confusing dosing instructions on label
4. When applicable, Problems with different manufacturer of same medicine: not getting same results from a generic drug as a brand name drug, or from another generic

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Sotradecol Reactions
AcneWhat is Acne?
Air Embolism
Alopecia
Anaphylactic Shock
AphasiaWhat is Aphasia?
Arthralgia
Cardiac ArrestWhat is Cardiac arrest?
Cerebral Artery Embolism
Chromaturia
Diarrhoea
Dysgeusia
Ear Discomfort
Erythema
Eschar
Eye Irritation
FallWhat is Fall?
Fatigue
Feeling Hot
HeadacheWhat is Headache?
Hemiparesis
Hyperhidrosis
Hypersensitivity
Hypertension
Hypotension
Immediate Post-injection Reaction
Loss Of Consciousness
Oxygen Saturation Decreased
Procedural Complication
Renal Failure Acute
UlcerWhat is Ulcer?
Sotradecol Side Effects Notice - The material on this site is for informational purposes only, and is not a substitute for medical advice, diagnosis or treatment provided by a qualified health care provider. PatientsVille.com does not provide medical advice, diagnosis or treatment. The information regarding Sotradecol adverse reports, reviews and polls contained on PatientsVille.com site has not been scientifically or otherwise verified as to a cause and effect relationship and cannot be used to estimate the incidence of adverse drug reactions or for establishing or changing of patient treatments. Thank you for visiting Patientsville.com!