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Summary

FDA Adverse Reports: 137. View All

Depodur FDA safety alerts: No

Reported deaths: 5

Reported hospitalizations: 63

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

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Showing 1-50 of 137  Next Page  >

6907424-9 | Respiratory Distress, Sleep Apnoea Syndrome
on Jan 27, 2010 Male patient from UNITED STATES , 62 years of age, weighting 303.0 lb, was diagnosed with hip arthroplasty and was treated with Depodur (View Usage). Patient experienced the following unwanted or unexpected effects: respiratory distress, sleep apnoea syndrome. Depodur dosage: 15 Mg;x1;ed.

6874637-4 | Anaemia Postoperative, Hypotension
Patient was taking Depodur (View Usage). Patient had the following side effects: anaemia postoperative, hypotension on Jul 09, 2010 from UNITED STATES Additional patient health information: Female patient , 66 years of age, weighting 271.2 lb, was diagnosed with procedural pain and. Depodur dosage: 10 Mg; X1; Ed. During the same period patient was treated with BETAPACE (View Betapace Review and Betapace Label ), DILAUDID (View Dilaudid Review and Dilaudid Label ), LASIX (View Lasix Review and Lasix Label ).

6479518-6 | Respiratory Arrest
Adverse event was reported on Dec 07, 2009 by a Male patient taking Depodur (View Usage) (Dosage: 10 Mg Once Intra) . Location: UNITED STATES , 57 years of age, weighting 140.0 lb, After Depodur was administered, patient had the following side effects: respiratory arrest.

6276415-6 | Hypotension, Tachycardia
on Aug 06, 2008 Female patient from UNITED STATES , 39 years of age, was diagnosed with procedural pain and was treated with Depodur (View Usage). Patient experienced the following unwanted or unexpected effects: hypotension, tachycardia. Depodur dosage: 15 Mg;1x;ed. During the same period patient was treated with VICODIN (View Vicodin Review and Vicodin Label ).


6276410-7 | Respiratory Depression
on Jun 05, 2008 Male patient from UNITED STATES , 61 years of age, was diagnosed with procedural pain and was treated with Depodur (View Usage). Patient had the following side effects: respiratory depression. Depodur dosage: 15 Mg;1x.

6276403-X | Respiratory Depression
Patient was taking Depodur (View Usage). After Depodur was administered, patient had the following side effects: respiratory depression on Mar 16, 2009 from UNITED STATES Additional patient health information: Male patient , 76 years of age, was diagnosed with procedural pain and. Depodur dosage: 15 Mg;1x;ed.

5822808-8 | Apnoea, Coma, Hypoxia, Sedation, Somnolence
Adverse event was reported on Feb 21, 2008 by a Female patient taking Depodur (View Usage) (Dosage: 5 Mg;1x;ed) was diagnosed with postoperative analgesia, nausea (What is nausea?) and. Location: UNITED STATES , 69 years of age, Patient experienced the following unwanted or unexpected effects: apnoea, coma, hypoxia, sedation, somnolence. During the same period patient was treated with TRANSDERM SCOP (1.5 Mg;1x;tder) (View Transderm Scop Review and Transderm Scop Label ). Patient was hospitalized.

5822806-4 | Hypotension
on May 06, 2008 Male patient from UNITED STATES , 42 years of age, weighting 245.0 lb, was diagnosed with procedural pain and was treated with Depodur (View Usage). Patient had the following side effects: hypotension. Depodur dosage: 10 Mg;x1;ed. During the same period patient was treated with IBUPROFEN (View Ibuprofen Review and Ibuprofen Label ), EXCEDRIN /00391201/ (View Excedrin /00391201/ Review and Excedrin /00391201/ Label ).

5822795-2 | Coma, Dysarthria, Hypotension
on May 06, 2008 Female patient from UNITED STATES , 54 years of age, weighting 164.0 lb, was diagnosed with procedural pain and was treated with Depodur (View Usage). After Depodur was administered, patient had the following side effects: coma, dysarthria, hypotension. Depodur dosage: 10 Mg;1x;ed. During the same period patient was treated with CLARITIN /00413701/ (View Claritin /00413701/ Review and Claritin /00413701/ Label ), SINGULAIR (View Singulair Review and Singulair Label ), ALBUTEROL (View Albuterol Review and Albuterol Label ), ZOLOFT (View Zoloft Review and Zoloft Label ), FOSAMAX (View Fosamax Review and Fosamax Label ), ADVANT (View Advant Review and Advant Label ), ESTROVEN /02150801/ (View Estroven /02150801/ Review and Estroven /02150801/ Label ).

5822761-7 | Hypotension
Patient was taking Depodur (View Usage). Patient experienced the following unwanted or unexpected effects: hypotension on Apr 23, 2008 from UNITED STATES Additional patient health information: Female patient , 66 years of age, was diagnosed with procedural pain and. Depodur dosage: 7.5 Mg;1x;ed. Patient was hospitalized.

5822743-5 | Respiratory Depression
Adverse event was reported on Mar 26, 2008 by a Female patient taking Depodur (View Usage) (Dosage: 10 Mg;1x;ed) was diagnosed with procedural pain and. Location: UNITED STATES , 70 years of age, Patient had the following side effects: respiratory depression.

5822706-X | Respiratory Depression
on Mar 26, 2008 Female patient from UNITED STATES , 74 years of age, was diagnosed with procedural pain and was treated with Depodur (View Usage). After Depodur was administered, patient had the following side effects: respiratory depression. Depodur dosage: 10 Mg;1x;ed. Patient was hospitalized.

5822705-8 | Respiratory Depression
on Feb 06, 2008 Female patient from UNITED STATES , 61 years of age, was diagnosed with procedural pain and was treated with Depodur (View Usage). Patient experienced the following unwanted or unexpected effects: respiratory depression. Depodur dosage: 10 Mg;x1;ed.

5822700-9 | Respiratory Depression
Patient was taking Depodur (View Usage). Patient had the following side effects: respiratory depression on Feb 06, 2008 from UNITED STATES Additional patient health information: Female patient , 44 years of age, was diagnosed with procedural pain and. Depodur dosage: 10 Mg;x1;ed.

5822687-9 | Hypertension, Nausea, Sedation, Tachycardia
Adverse event was reported on Sep 04, 2007 by a Female patient taking Depodur (View Usage) (Dosage: 7.5 Mg;1x;inth) was diagnosed with pain management and. Location: UNITED STATES , 45 years of age, After Depodur was administered, patient had the following side effects: hypertension, nausea (What is nausea?), sedation, tachycardia. During the same period patient was treated with FENTANYL (View Fentanyl Review and Fentanyl Label ).

5747962-8 | Hypotension, Hypoxia, Myocardial Infarction, Somnolence, Unresponsive To Stimuli
on May 06, 2008 Male patient from UNITED STATES , 58 years of age, weighting 246.0 lb, was diagnosed with procedural pain and was treated with Depodur (View Usage). Patient experienced the following unwanted or unexpected effects: hypotension, hypoxia, myocardial infarction, somnolence, unresponsive to stimuli. Depodur dosage: 12.5 Mg;1x; Ed. During the same period patient was treated with VERAPAMIL (View Verapamil Review and Verapamil Label ), CLONIDINE (View Clonidine Review and Clonidine Label ), TERAZOSIN (View Terazosin Review and Terazosin Label ), LASIX /00032601/ (View Lasix /00032601/ Review and Lasix /00032601/ Label ), QUINIDINE HCL (View Quinidine Hcl Review and Quinidine Hcl Label ), VICODIN (View Vicodin Review and Vicodin Label ), OXYCONTIN (View Oxycontin Review and Oxycontin Label ), TIZADINE (View Tizadine Review and Tizadine Label ).

5735399-7 | Nausea, Pruritus
on May 08, 2008 Female patient from UNITED STATES , 34 years of age, weighting 162.0 lb, was treated with Depodur (View Usage). Patient had the following side effects: nausea (What is nausea?), pruritus. Depodur dosage: .

5703551-2 | Aspiration, Obstructive Airways Disorder, Respiratory Depression
Patient was taking Depodur (View Usage). After Depodur was administered, patient had the following side effects: aspiration, obstructive airways disorder, respiratory depression on Mar 26, 2008 from UNITED STATES Additional patient health information: Female patient , 72 years of age, was diagnosed with procedural pain and. Depodur dosage: 7.5 Mg; 1x; Ed. Patient was hospitalized.

5509730-1 | Hypotension, Respiratory Depression
Adverse event was reported on Nov 07, 2007 by a Female patient taking Depodur (View Usage) (Dosage: Depodur 10mg X1 Epidural) was diagnosed with preoperative care and. Location: UNITED STATES , 76 years of age, weighting 136.0 lb, Patient experienced the following unwanted or unexpected effects: hypotension, respiratory depression. Patient was hospitalized.

5509729-5 | Blood Pressure Decreased, Respiratory Rate Decreased
on Nov 07, 2007 Female patient from UNITED STATES , 57 years of age, weighting 178.6 lb, was diagnosed with preoperative care and was treated with Depodur (View Usage). Patient had the following side effects: blood pressure decreased, respiratory rate decreased. Depodur dosage: Depodur 7.5mgx1 Epidural. Patient was hospitalized.

5509728-3 | Respiratory Rate Decreased
on Nov 07, 2007 Male patient from UNITED STATES , 81 years of age, weighting 167.6 lb, was diagnosed with preoperative care and was treated with Depodur (View Usage). After Depodur was administered, patient had the following side effects: respiratory rate decreased. Depodur dosage: Depodur 8 Mg X1 Epidural. Patient was hospitalized.

5509727-1 | Anuria, Hypotension, Respiratory Distress
Patient was taking Depodur (View Usage). Patient experienced the following unwanted or unexpected effects: anuria, hypotension, respiratory distress on Nov 07, 2007 from UNITED STATES Additional patient health information: Female patient , 74 years of age, weighting 140.0 lb, . Depodur dosage: Depodur 3mg X 1 Epidural.

5509726-X | Blood Pressure Decreased, No Therapeutic Response, Respiratory Rate Decreased
Adverse event was reported on Nov 07, 2007 by a Female patient taking Depodur (View Usage) (Dosage: Depodur 10 Mg X1 Epidural) was diagnosed with anaesthesia, preoperative care and. Location: UNITED STATES , 56 years of age, weighting 240.3 lb, Patient had the following side effects: blood pressure decreased, no therapeutic response, respiratory rate decreased.

5509666-6 | Blood Pressure Decreased, Heart Rate Decreased, Respiratory Rate Decreased
on Nov 07, 2007 Female patient from UNITED STATES , 82 years of age, weighting 134.0 lb, was diagnosed with anaesthesia and was treated with Depodur (View Usage). After Depodur was administered, patient had the following side effects: blood pressure decreased, heart rate decreased, respiratory rate decreased. Depodur dosage: 10mg X 1 Epidural.

5509665-4 | Hypotension, Respiratory Depression
on Nov 07, 2007 Female patient from UNITED STATES , 59 years of age, weighting 156.5 lb, was diagnosed with anaesthesia and was treated with Depodur (View Usage). Patient experienced the following unwanted or unexpected effects: hypotension, respiratory depression. Depodur dosage: 7mg X1 Epidural.

5487978-2 | Respiratory Depression, Sedation
Patient was taking Depodur (View Usage). Patient had the following side effects: respiratory depression, sedation on Oct 12, 2007 from UNITED STATES Additional patient health information: Female patient , 71 years of age, weighting 200.0 lb, was diagnosed with knee operation, pain management and. Depodur dosage: 7.5 Mg Once Epidural.

5398962-1 | Respiratory Depression
Adverse event was reported on Jul 24, 2007 by a Female patient taking Depodur (View Usage) (Dosage: 10 Mg Once Epidural) was diagnosed with knee arthroplasty, pain management, postoperative care and. Location: UNITED STATES , weighting 229.3 lb, After Depodur was administered, patient had the following side effects: respiratory depression.

5397524-X | Hypoventilation, Oxygen Saturation Decreased, Respiratory Acidosis, Sedation
on Jul 24, 2007 Female patient from UNITED STATES , 68 years of age, weighting 164.0 lb, was diagnosed with pain (What is pain?) and was treated with Depodur (View Usage). Patient experienced the following unwanted or unexpected effects: hypoventilation, oxygen saturation decreased, respiratory acidosis, sedation. Depodur dosage: 11 Mg Epidural. During the same period patient was treated with ASPIRIN (View Aspirin Review and Aspirin Label ), DOCUSATE (View Docusate Review and Docusate Label ), CEFAZOLIN (View Cefazolin Review and Cefazolin Label ), ESOMEPRAZOLE MAGNESIUM (View Esomeprazole Magnesium Review and Esomeprazole Magnesium Label ), URSODIOL (View Ursodiol Review and Ursodiol Label ), CITALOPRAM HYDROBROMIDE (View Citalopram Hydrobromide Review and Citalopram Hydrobromide Label ), GLYCOPYRROLATE (View Glycopyrrolate Review and Glycopyrrolate Label ).

5372108-8 | Hypoxia
on Feb 20, 2007 Female patient from UNITED STATES , 57 years of age, weighting 294.0 lb, was diagnosed with procedural pain and was treated with Depodur (View Usage). Patient had the following side effects: hypoxia. Depodur dosage: 10 Mg;x1;ed. During the same period patient was treated with MORPHINE (View Morphine Review and Morphine Label ), PERCOCET (View Percocet Review and Percocet Label ), TYLENOL (CAPLET) (View Tylenol (caplet) Review and Tylenol (caplet) Label ).

5345431-0 | Fall, Loss Of Consciousness, Pulmonary Embolism, Pulse Absent
Patient was taking Depodur (View Usage). After Depodur was administered, patient had the following side effects: fall (What is fall?), loss of consciousness, pulmonary embolism (What is pulmonary embolism?), pulse absent on May 21, 2007 from UNITED STATES Additional patient health information: Male patient , 54 years of age, was diagnosed with postoperative analgesia and. Depodur dosage: 20 Mg; X1; Ed.

5337854-0 | Hypotension, Respiratory Depression
Adverse event was reported on Dec 13, 2006 by a Female patient taking Depodur (View Usage) (Dosage: 10 Mg;) . Location: UNITED STATES , 71 years of age, Patient experienced the following unwanted or unexpected effects: hypotension, respiratory depression.

5337853-9 | Gait Disturbance, Ileus, Oxygen Saturation Decreased, Pruritus, Sedation
on Jan 26, 2007 Female patient from UNITED STATES , 63 years of age, weighting 258.0 lb, was diagnosed with procedural pain and was treated with Depodur (View Usage). Patient had the following side effects: gait disturbance, ileus, oxygen saturation decreased, pruritus, sedation. Depodur dosage: 10 Mg;x1;ed. During the same period patient was treated with MORPHINE (View Morphine Review and Morphine Label ), VERSED (View Versed Review and Versed Label ), FENTANYL (View Fentanyl Review and Fentanyl Label ), TORADOL (View Toradol Review and Toradol Label ). Patient was hospitalized.

5314307-7 | Arthralgia, Confusional State, Hypoventilation, Iatrogenic Injury, Loss Of Consciousness, Respiratory Depression, Respiratory Disorder, Respiratory Distress
on Mar 07, 2007 Female patient from UNITED STATES , 70 years of age, weighting 147.7 lb, was diagnosed with pain (What is pain?) and was treated with Depodur (View Usage). After Depodur was administered, patient had the following side effects: arthralgia, confusional state, hypoventilation, iatrogenic injury, loss of consciousness, respiratory depression, respiratory disorder, respiratory distress. Depodur dosage: 15 Mg; X1; Ed. During the same period patient was treated with VERSED (View Versed Review and Versed Label ), FENTANYL (View Fentanyl Review and Fentanyl Label ), PROPOFOL (View Propofol Review and Propofol Label ), HYDROCODONE BITARTRATE + ACETAMINOPHEN (View Hydrocodone Bitartrate + Acetaminophen Review and Hydrocodone Bitartrate + Acetaminophen Label ).

5314306-5 | Coma, Pain, Respiratory Depression
Patient was taking Depodur (View Usage). Patient experienced the following unwanted or unexpected effects: coma, pain (What is pain?), respiratory depression on Mar 21, 2007 from UNITED STATES Additional patient health information: Female patient , 68 years of age, was diagnosed with pain (What is pain?) and. Depodur dosage: 15 Mg; X1; Ed.

5293995-8 | Anaesthetic Complication, Arthralgia, Body Temperature Decreased, Confusion Postoperative, Dyspnoea, Loss Of Consciousness, Procedural Complication, Respiratory Depression
Adverse event was reported on Mar 07, 2007 by a Female patient taking Depodur (View Usage) (Dosage: 15 Mg;x1;ed) was diagnosed with pain (What is pain?) and. Location: UNITED STATES , 70 years of age, weighting 147.7 lb, Patient had the following side effects: anaesthetic complication, arthralgia, body temperature decreased, confusion postoperative, dyspnoea, loss of consciousness, procedural complication, respiratory depression. During the same period patient was treated with VERSED (View Versed Review and Versed Label ), FENTANYL (View Fentanyl Review and Fentanyl Label ), PROPOFOL (View Propofol Review and Propofol Label ), HYDROCODONE BITARTRATE + ACETAMINOPHEN (View Hydrocodone Bitartrate + Acetaminophen Review and Hydrocodone Bitartrate + Acetaminophen Label ).

5293994-6 | Pain, Respiratory Depression, Unresponsive To Stimuli
on Mar 21, 2007 Female patient from UNITED STATES , 68 years of age, was diagnosed with pain (What is pain?) and was treated with Depodur (View Usage). After Depodur was administered, patient had the following side effects: pain (What is pain?), respiratory depression, unresponsive to stimuli. Depodur dosage: 15 Mg;x1;ed.

5259507-X | Anoxic Encephalopathy, Blood Gases Abnormal, Blood Pressure Decreased, Respiratory Depression
on Jul 26, 2006 Female patient from UNITED STATES , 78 years of age, weighting 190.2 lb, was diagnosed with procedural pain and was treated with Depodur (View Usage). Patient experienced the following unwanted or unexpected effects: anoxic encephalopathy, blood gases abnormal, blood pressure decreased, respiratory depression. Depodur dosage: 10 Mg;x1;ed. During the same period patient was treated with BUPIVACAINE (View Bupivacaine Review and Bupivacaine Label ). Patient was hospitalized.

5259505-6 | Ileus, Oxygen Saturation Decreased, Pruritus, Sedation
Patient was taking Depodur (View Usage). Patient had the following side effects: ileus, oxygen saturation decreased, pruritus, sedation on Oct 02, 2006 from UNITED STATES Additional patient health information: Female patient , 63 years of age, weighting 258.0 lb, was diagnosed with procedural pain and. Depodur dosage: 10 Mg;x1;ed. During the same period patient was treated with MORPHINE (View Morphine Review and Morphine Label ), VERSED (View Versed Review and Versed Label ), FENTANYL (View Fentanyl Review and Fentanyl Label ), NARCAN (View Narcan Review and Narcan Label ), TORADOL (View Toradol Review and Toradol Label ). Patient was hospitalized.

5238089-2 | Condition Aggravated, Heart Rate Decreased
Adverse event was reported on Feb 09, 2007 by a Female patient taking Depodur (View Usage) (Dosage: 7 Mg Once Epidural) was diagnosed with postoperative analgesia and. Location: UNITED STATES , weighting 169.8 lb, After Depodur was administered, patient had the following side effects: condition aggravated, heart rate decreased. Patient was hospitalized.

5237075-6 | Gait Disturbance, Haemorrhage, Ileus, Nervous System Disorder, Oxygen Saturation Decreased, Pruritus, Sedation
on Jan 26, 2007 Female patient from UNITED STATES , 63 years of age, weighting 258.0 lb, was diagnosed with pain (What is pain?), post procedural complication and was treated with Depodur (View Usage). Patient experienced the following unwanted or unexpected effects: gait disturbance, haemorrhage, ileus, nervous system disorder, oxygen saturation decreased, pruritus, sedation. Depodur dosage: 10 Mg; X1; Ed. During the same period patient was treated with MORPHINE (View Morphine Review and Morphine Label ), VERSED (View Versed Review and Versed Label ), FENTANYL (View Fentanyl Review and Fentanyl Label ), TORADOL (View Toradol Review and Toradol Label ). Patient was hospitalized.

5236645-9 | Loss Of Consciousness, Respiratory Depression, Somnolence
on Jan 26, 2007 Female patient from UNITED STATES , 70 years of age, weighting 149.0 lb, was diagnosed with procedural pain and was treated with Depodur (View Usage). Patient had the following side effects: loss of consciousness, respiratory depression, somnolence. Depodur dosage: 15 Mg X1 Ed.

5236598-3 | Abdominal Infection, Haemodialysis, Hypotension, Intestinal Ischaemia, Pain, Post Procedural Complication, Renal Failure, Restlessness
Patient was taking Depodur (View Usage). After Depodur was administered, patient had the following side effects: abdominal infection, haemodialysis, hypotension, intestinal ischaemia, pain (What is pain?), post procedural complication, renal failure, restlessness on Jan 17, 2007 from UNITED STATES Additional patient health information: Female patient , 67 years of age, was diagnosed with pain (What is pain?) and. Depodur dosage: 10 Mg; X1; Ed. During the same period patient was treated with MORPHINE SULFATE (View Morphine Sulfate Review and Morphine Sulfate Label ).

5162460-0 | Abasia, Anaesthetic Complication, Sedation
Adverse event was reported on Nov 28, 2006 by a Female patient taking Depodur (View Usage) (Dosage: 10 Mg Epidurally) was diagnosed with pain management and. Location: UNITED STATES , weighting 258.0 lb, Patient experienced the following unwanted or unexpected effects: abasia, anaesthetic complication, sedation. Patient was hospitalized.

5145240-1 | Blood Pressure Decreased, Respiratory Depression
on Jul 26, 2006 Female patient from UNITED STATES , 78 years of age, weighting 190.0 lb, was diagnosed with procedural pain and was treated with Depodur (View Usage). Patient had the following side effects: blood pressure decreased, respiratory depression. Depodur dosage: 10 Mg (once),epidural. Patient was hospitalized.

5145235-8 | Respiratory Depression
on Jul 14, 2006 Female patient from UNITED STATES , 70 years of age, was diagnosed with procedural pain and was treated with Depodur (View Usage). After Depodur was administered, patient had the following side effects: respiratory depression. Depodur dosage: .

5145234-6 | Apnoea, Respiratory Depression, Respiratory Rate Decreased
Patient was taking Depodur (View Usage). Patient experienced the following unwanted or unexpected effects: apnoea, respiratory depression, respiratory rate decreased on Jun 05, 2006 from UNITED STATES Additional patient health information: Female patient , 75 years of age, weighting 165.3 lb, was diagnosed with postoperative analgesia and. Depodur dosage: (10 Mg,1 Once),epidural. During the same period patient was treated with GLUCOSAMINE (GLUCOSAMINE) (View Glucosamine (glucosamine) Review and Glucosamine (glucosamine) Label ), CHONDROITIN (View Chondroitin Review and Chondroitin Label ).

5108837-0 | Dyspnoea, Hypoxia, Post Procedural Complication
Adverse event was reported on Sep 15, 2006 by a Female patient taking Depodur (View Usage) (Dosage: 10mg One Time Dose Im) was diagnosed with postoperative analgesia and. Location: UNITED STATES , 64 years of age, weighting 282.2 lb, Patient had the following side effects: dyspnoea, hypoxia, post procedural complication. Patient was hospitalized and became disabled.

5103627-7 | Blood Pressure Decreased
on Sep 11, 2006 Female patient from UNITED STATES , weighting 185.2 lb, was diagnosed with surgery (What is surgery?) and was treated with Depodur (View Usage). After Depodur was administered, patient had the following side effects: blood pressure decreased. Depodur dosage: 10mg Once Epidural. Patient was hospitalized.

5100678-3 | Anoxic Encephalopathy, Blood Gases Abnormal, Blood Pressure Decreased, Pco2 Increased, Po2 Increased, Respiratory Depression, Sleep Apnoea Syndrome
on Aug 22, 2006 Female patient from UNITED STATES , 78 years of age, weighting 190.0 lb, was diagnosed with procedural pain and was treated with Depodur (View Usage). Patient experienced the following unwanted or unexpected effects: anoxic encephalopathy, blood gases abnormal, blood pressure decreased, pco2 increased, po2 increased, respiratory depression, sleep apnoea syndrome. Depodur dosage: 10 Mg (once), Epidural. During the same period patient was treated with BUPIVACAINE (View Bupivacaine Review and Bupivacaine Label ). Patient was hospitalized.

5067438-3 | Blood Pressure Diastolic Decreased, Blood Pressure Systolic Increased, Body Temperature Increased, Heart Rate Increased, Loss Of Consciousness, Oxygen Saturation Decreased, Post Procedural Complication, Respiratory Depression, Respiratory Rate Decreased
Patient was taking Depodur (View Usage). Patient had the following side effects: blood pressure diastolic decreased, blood pressure systolic increased, body temperature increased, heart rate increased, loss of consciousness, oxygen saturation decreased, post procedural complication, respiratory depression, respiratory rate decreased on Jul 14, 2006 from UNITED STATES Additional patient health information: Female patient , 66 years of age, weighting 258.0 lb, was diagnosed with procedural pain and. Depodur dosage: 10 Mg, Epidural. During the same period patient was treated with FENTANYL (View Fentanyl Review and Fentanyl Label ), VERSED (View Versed Review and Versed Label ), ZOFRAN (View Zofran Review and Zofran Label ), PERCOSET (TYLOX/00446701/) (View Percoset (tylox/00446701/) Review and Percoset (tylox/00446701/) Label ), MORPHINE SULFATE (View Morphine Sulfate Review and Morphine Sulfate Label ). Patient was hospitalized.

Showing 1-50 of 137  Next Page  >


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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 Depodur 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 Depodur quality problem: suspected counterfeit product, potentially contaminated product indicated by suspicious odor or unusual color, inaccurate or unreadable product labeling
3. Potential Depodur 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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depodur Episodes: 3: Diagnosed with major depression.Side effects: cardiac failure, myocarditis More: desloratadine Episodes: 2: Diagnosed with major depression ...

depodur Episodes: 1: Diagnosed with major depression.Side effects: cardiac failure, myocarditis More: duragesic Episodes: 6: Diagnosed with major depression.Side ...

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depodur Episodes: 5: Diagnosed with major depression.Side effects: cardiac failure, myocarditis More: deroxat Episodes: 6: Diagnosed with major depression.Side ...

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Depodur Reactions
Anaesthetic Complication
Apnoea
Blood Pressure Decreased
Bradycardia
Cardiac ArrestWhat is Cardiac arrest?
Coma
Depressed Level Of Consciousness
Dyspnoea
Heart Rate Increased
Hypotension
Hypoventilation
Hypoxia
Lethargy
Loss Of Consciousness
Myocardial Infarction
NauseaWhat is Nausea?
Oxygen Saturation Decreased
PainWhat is Pain?
Pco2 Increased
Post Procedural Complication
Procedural Complication
Pruritus
Pulmonary EmbolismWhat is Pulmonary embolism?
Renal Failure
Respiratory Acidosis
Respiratory Arrest
Respiratory Depression
Respiratory Rate Decreased
Sedation
Somnolence
Depodur 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 Depodur 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!