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Niopam adverse events reported to FDA.

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Summary

FDA Adverse Reports: 10. View All

Niopam FDA safety alerts: No

Reported deaths: 7

Reported hospitalizations: 1

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

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6600921-5 | Arteriosclerosis Coronary Artery, Cardiac Arrest, Hepatic Congestion, Pulmonary Congestion, Respiratory Arrest
on Feb 16, 2010 Female patient from UNITED KINGDOM , weighting 138.9 lb, was diagnosed with computerised tomogram and was treated with Niopam (View Usage). Patient experienced the following unwanted or unexpected effects: arteriosclerosis coronary artery, cardiac arrest (What is cardiac arrest?), hepatic congestion, pulmonary congestion, respiratory arrest. Niopam dosage: . During the same period patient was treated with GLICLAZIDE (View Gliclazide Review and Gliclazide Label ), METFORMIN HCL (View Metformin Hcl Review and Metformin Hcl Label ), ASPIRIN (Dispersible) (View Aspirin Review and Aspirin Label ), RAMIPRIL (View Ramipril Review and Ramipril Label ), CLOMIPRAMINE HCL (View Clomipramine Hcl Review and Clomipramine Hcl Label ), FUROSEMIDE (View Furosemide Review and Furosemide Label ).

5321019-2 | Anaphylactic Reaction
Patient was taking Niopam (View Usage). Patient had the following side effects: anaphylactic reaction on May 04, 2007 from UNITED KINGDOM Additional patient health information: Female patient , weighting 154.3 lb, was diagnosed with arteriovenous fistula site complication and. Niopam dosage: . During the same period patient was treated with ALFACALCIDOL (View Alfacalcidol Review and Alfacalcidol Label ), AMITRIPTYLINE HCL (View Amitriptyline Hcl Review and Amitriptyline Hcl Label ), EPOGEN (View Epogen Review and Epogen Label ), CO DYDRAMOL (View Co-dydramol Review and Co-dydramol Label ), KETOVITE /00479801/ (View Ketovite /00479801/ Review and Ketovite /00479801/ Label ), OMEPRAZOLE (View Omeprazole Review and Omeprazole Label ).

5306967-1 | Dermatitis Exfoliative
Adverse event was reported on Apr 19, 2007 by a Female patient taking Niopam (View Usage) (Dosage: ) . Location: UNITED KINGDOM , 54 years of age, After Niopam was administered, patient had the following side effects: dermatitis exfoliative. During the same period patient was treated with ATROVENT (View Atrovent Review and Atrovent Label ), METHOTREXATE (View Methotrexate Review and Methotrexate Label ), SYMBICORT (View Symbicort Review and Symbicort Label ). Patient was hospitalized.

5289295-2 | Anaphylactic Reaction, Arteriosclerosis Coronary Artery, Cardio-respiratory Arrest, Contrast Media Reaction, Convulsion
on Mar 30, 2007 Female patient from UNITED KINGDOM , weighting 154.3 lb, was diagnosed with arteriovenous fistula site complication and was treated with Niopam (View Usage). Patient experienced the following unwanted or unexpected effects: anaphylactic reaction, arteriosclerosis coronary artery, cardio-respiratory arrest, contrast media reaction, convulsion. Niopam dosage: . During the same period patient was treated with ALFACALCIDOL (View Alfacalcidol Review and Alfacalcidol Label ), AMITRIPTYLINE HCL (View Amitriptyline Hcl Review and Amitriptyline Hcl Label ), EPOGEN (View Epogen Review and Epogen Label ), CO DYDRAMOL (View Co-dydramol Review and Co-dydramol Label ), KETOVITE /00479801/ (View Ketovite /00479801/ Review and Ketovite /00479801/ Label ), OMEPRAZOLE (View Omeprazole Review and Omeprazole Label ).


5269436-3 | Anaphylactic Reaction
on Mar 12, 2007 Female patient from UNITED KINGDOM , 75 years of age, weighting 154.3 lb, was treated with Niopam (View Usage). Patient had the following side effects: anaphylactic reaction. Niopam dosage: .

5113693-0 | Anaphylactic Reaction
Patient was taking Niopam (View Usage). After Niopam was administered, patient had the following side effects: anaphylactic reaction on Jun 09, 2006 from UNITED KINGDOM Additional patient health information: Female patient , weighting 143.3 lb, was diagnosed with arteriovenous fistula site complication and. Niopam dosage: . During the same period patient was treated with ALFACALCIDOL (View Alfacalcidol Review and Alfacalcidol Label ), AMITRIPTYLINE HCL (View Amitriptyline Hcl Review and Amitriptyline Hcl Label ), EPOGEN (View Epogen Review and Epogen Label ), CO DYDRAMOL (View Co-dydramol Review and Co-dydramol Label ), KETOVITE /00479801/ (View Ketovite /00479801/ Review and Ketovite /00479801/ Label ), OMEPRAZOLE (View Omeprazole Review and Omeprazole Label ).

5095952-3 | Muscular Weakness, Rash
Adverse event was reported on Aug 29, 2006 by a Female patient taking Niopam (View Usage) (Dosage: ) . Location: UNITED KINGDOM , 34 years of age, Patient experienced the following unwanted or unexpected effects: muscular weakness, rash (What is rash?). During the same period patient was treated with THYROXINE (View Thyroxine Review and Thyroxine Label ), STEROIDS (View Steroids Review and Steroids Label ).

5085119-7 | Anaphylactic Reaction
on Jun 09, 2006 Female patient from UNITED KINGDOM , weighting 143.3 lb, was diagnosed with arteriovenous fistula site complication and was treated with Niopam (View Usage). Patient had the following side effects: anaphylactic reaction. Niopam dosage: . During the same period patient was treated with ALFACALCIDOL (View Alfacalcidol Review and Alfacalcidol Label ), AMITRIPTYLINE HCL (View Amitriptyline Hcl Review and Amitriptyline Hcl Label ), EPOGEN (View Epogen Review and Epogen Label ), CO DYDRAMOL (View Co-dydramol Review and Co-dydramol Label ), KETOVITE /00479801/ (View Ketovite /00479801/ Review and Ketovite /00479801/ Label ), OMEPRAZOLE (View Omeprazole Review and Omeprazole Label ).

5051003-8 | Anaphylactic Reaction, Cardiac Arrest
on Jul 05, 2006 Male patient from UNITED KINGDOM , 45 years of age, was diagnosed with percutaneous coronary intervention and was treated with Niopam (View Usage). After Niopam was administered, patient had the following side effects: anaphylactic reaction, cardiac arrest (What is cardiac arrest?). Niopam dosage: . During the same period patient was treated with IOHEXOL (View Iohexol Review and Iohexol Label ), BIVALIRUDIN (View Bivalirudin Review and Bivalirudin Label ).

4947985-2 | Bile Duct Necrosis, Blood Creatinine Increased, Cardio-respiratory Arrest, Cyanosis, Diffuse Alveolar Damage, Jaundice, Lymphopenia, Nephritis
Patient was taking Niopam (View Usage). Patient experienced the following unwanted or unexpected effects: bile duct necrosis, blood creatinine increased, cardio-respiratory arrest, cyanosis, diffuse alveolar damage, jaundice (What is jaundice?), lymphopenia, nephritis on Mar 14, 2006 from UNITED KINGDOM Additional patient health information: Female patient , 46 years of age, . Niopam dosage: .


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Niopam Questions, Answers, Feedback and Comments

Comments to date: 1. Page 1 of 1.

ayman baz   lebanon

5:19pm on Sunday, April 10th, 2011

i would to have full information about niopam and if i can be the execlusive distributor in middele ... read more »

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 Niopam 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 Niopam quality problem: suspected counterfeit product, potentially contaminated product indicated by suspicious odor or unusual color, inaccurate or unreadable product labeling
3. Potential Niopam 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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Niopam Reactions
Anaphylactic Reaction
Arteriosclerosis Coronary Artery
Bile Duct Necrosis
Blood Creatinine Increased
Cardiac ArrestWhat is Cardiac arrest?
Cardio-respiratory Arrest
Contrast Media Reaction
Convulsion
Cyanosis
Dermatitis Exfoliative
Diffuse Alveolar Damage
Hepatic Congestion
JaundiceWhat is Jaundice?
Lymphopenia
Muscular Weakness
Nephritis
Pulmonary Congestion
RashWhat is Rash?
Respiratory Arrest
Niopam 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 Niopam 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!