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Scandicain adverse events reported to FDA.

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Summary

FDA Adverse Reports: 10. View All

Scandicain FDA safety alerts: No

Reported hospitalizations: 2

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Often additional risks of using a medication, such as Scandicain, 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 Scandicain users, Learn more about unwanted side effects & find ways to reduce them. Browse Scandicain Adverse Reports reported to FDA and participate in Scandicain discussion, find alternative treatments and find ways to avoid or reduce risks associated with using Scandicain. 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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Scandicain Adverse Effect Reports (FDA)

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6101487-9 | Embolia Cutis Medicamentosa
on Feb 24, 2009 Female patient from GERMANY , 29 years of age, was diagnosed with anaesthesia and was treated with Scandicain (View Usage). Patient experienced the following unwanted or unexpected effects: embolia cutis medicamentosa. Scandicain dosage: . During the same period patient was treated with ROPIVACAIN (View Ropivacain Review and Ropivacain Label ). Patient was hospitalized.

5810553-4 | Retinal Artery Occlusion
Patient was taking Scandicain (View Usage). Patient had the following side effects: retinal artery occlusion on Jul 09, 2008 from SWITZERLAND Additional patient health information: Female patient , weighting 136.7 lb, was diagnosed with vitrectomy, hypercholesterolaemia and. Scandicain dosage: . During the same period patient was treated with SIMCORA 80 (View Simcora 80 Review and Simcora 80 Label ).

5810538-8 | Retinal Artery Occlusion
Adverse event was reported on Jul 09, 2008 by a Female patient taking Scandicain (View Usage) (Dosage: ) was diagnosed with vitrectomy and. Location: SWITZERLAND , weighting 123.5 lb, After Scandicain was administered, patient had the following side effects: retinal artery occlusion.

5810535-2 | Retinal Artery Occlusion
on Jul 09, 2008 Female patient from SWITZERLAND , weighting 191.8 lb, was diagnosed with vitrectomy and was treated with Scandicain (View Usage). Patient experienced the following unwanted or unexpected effects: retinal artery occlusion. Scandicain dosage: .


5809865-X | Retinal Artery Occlusion
on Jul 09, 2008 Male patient from SWITZERLAND , weighting 172.0 lb, was diagnosed with vitrectomy, haemodilution, hypertension, arteriosclerosis and was treated with Scandicain (View Usage). Patient had the following side effects: retinal artery occlusion. Scandicain dosage: . During the same period patient was treated with ASPIRIN (View Aspirin Review and Aspirin Label ), BELOK ZOK 25 (View Belok Zok 25 Review and Belok Zok 25 Label ), ALDACTONE 25 (View Aldactone 25 Review and Aldactone 25 Label ), SORTIS (View Sortis Review and Sortis Label ).

5809832-6 | Retinal Artery Occlusion
Patient was taking Scandicain (View Usage). After Scandicain was administered, patient had the following side effects: retinal artery occlusion on Jul 09, 2008 from SWITZERLAND Additional patient health information: Male patient , weighting 187.4 lb, was diagnosed with vitrectomy, diabetes mellitus, hypertension, platelet aggregation inhibition and. Scandicain dosage: . During the same period patient was treated with LISITRIL 12/5 (View Lisitril 12/5 Review and Lisitril 12/5 Label ), AMARYL 3 MG (View Amaryl 3 Mg Review and Amaryl 3 Mg Label ), AMLOPIN 10 (View Amlopin 10 Review and Amlopin 10 Label ), ASPIRIN (View Aspirin Review and Aspirin Label ).

5808885-9 | Retinal Artery Occlusion
Adverse event was reported on Jul 09, 2008 by a Female patient taking Scandicain (View Usage) (Dosage: ) was diagnosed with vitrectomy, cardiac valve prosthesis user, blood pressure (What is blood pressure?), hypertension and. Location: SWITZERLAND , weighting 130.1 lb, Patient experienced the following unwanted or unexpected effects: retinal artery occlusion. During the same period patient was treated with TIATRAL (View Tiatral Review and Tiatral Label ), MARCUMAR (View Marcumar Review and Marcumar Label ), SIMCORA 20 (View Simcora 20 Review and Simcora 20 Label ), FELODIL (View Felodil Review and Felodil Label ).

5808880-X | Retinal Artery Occlusion
on Jul 09, 2008 Female patient from SWITZERLAND , weighting 141.1 lb, was diagnosed with vitrectomy and was treated with Scandicain (View Usage). Patient had the following side effects: retinal artery occlusion. Scandicain dosage: .

5808877-X | Retinal Artery Occlusion
on Jul 09, 2008 Male patient from SWITZERLAND , weighting 222.7 lb, was diagnosed with vitrectomy and was treated with Scandicain (View Usage). After Scandicain was administered, patient had the following side effects: retinal artery occlusion. Scandicain dosage: .

4740561-6 | Bradypnoea, Depressed Level Of Consciousness, Myalgia, Rash
Patient was taking Scandicain (View Usage). Patient experienced the following unwanted or unexpected effects: bradypnoea, depressed level of consciousness, myalgia, rash (What is rash?) on Aug 04, 2005 from SWITZERLAND Additional patient health information: Female patient , 23 years of age, was diagnosed with allergy test and. Scandicain dosage: . 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 Scandicain 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 Scandicain quality problem: suspected counterfeit product, potentially contaminated product indicated by suspicious odor or unusual color, inaccurate or unreadable product labeling
3. Potential Scandicain 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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Scandicain Reactions
Bradypnoea
Depressed Level Of Consciousness
Embolia Cutis Medicamentosa
Myalgia
RashWhat is Rash?
Retinal Artery Occlusion
Scandicain 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 Scandicain 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!