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Propofan adverse events reported to FDA.

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FDA Adverse Reports: 3. View All

Propofan FDA safety alerts: No

Reported hospitalizations: 3

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

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5802286-5 | Arterial Thrombosis Limb
on Jun 27, 2008 Male patient from FRANCE , 74 years of age, weighting 198.4 lb, was treated with Propofan (View Usage). Patient experienced the following unwanted or unexpected effects: arterial thrombosis limb. Propofan dosage: . During the same period patient was treated with LERCAN (View Lercan Review and Lercan Label ), FLUDEX LP (View Fludex Lp Review and Fludex Lp Label ), STAGID (View Stagid Review and Stagid Label ), PRAVASTATIN (View Pravastatin Review and Pravastatin Label ), SECTRAL LP (View Sectral Lp Review and Sectral Lp Label ), PLAVIX (View Plavix Review and Plavix Label ). Patient was hospitalized.

5536919-8 | Acute Coronary Syndrome, Coronary Angioplasty, Coronary Artery Thrombosis
Patient was taking Propofan (View Usage). Patient had the following side effects: acute coronary syndrome, coronary angioplasty, coronary artery thrombosis on Dec 05, 2007 from FRANCE Additional patient health information: Male patient , 74 years of age, weighting 167.6 lb, was diagnosed with hypertension and. Propofan dosage: . During the same period patient was treated with PARACETAMOL (View Paracetamol Review and Paracetamol Label ), ROCGEL (View Rocgel Review and Rocgel Label ), PERIDYS (View Peridys Review and Peridys Label ), EXFORGE (1 Df, Qd) (View Exforge Review and Exforge Label ), ALLOPURINOL (100 Mg, Qd) (View Allopurinol Review and Allopurinol Label ). Patient was hospitalized and became disabled.

5519035-0 | Acute Coronary Syndrome, Coronary Angioplasty
Adverse event was reported on Nov 12, 2007 by a Male patient taking Propofan (View Usage) (Dosage: ) was diagnosed with hypertension and. Location: FRANCE , 74 years of age, After Propofan was administered, patient had the following side effects: acute coronary syndrome, coronary angioplasty. During the same period patient was treated with PARACETAMOL (View Paracetamol Review and Paracetamol Label ), ROCGEL (View Rocgel Review and Rocgel Label ), PERIDYS (View Peridys Review and Peridys Label ), EXFORGE (1 Df, Qd) (View Exforge Review and Exforge 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 Propofan 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 Propofan quality problem: suspected counterfeit product, potentially contaminated product indicated by suspicious odor or unusual color, inaccurate or unreadable product labeling
3. Potential Propofan 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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Propofan Reactions
Acute Coronary Syndrome
Arterial Thrombosis Limb
Coronary Angioplasty
Coronary Artery Thrombosis
Propofan 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 Propofan 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!