PROPOFOL Side Effects

6856806-2 | Haematuria, Post Procedural Complication, Renal Failure Acute
on Jun 16, 2010 Female patient from FRANCE , 17 years of age, was diagnosed with induction of anaesthesia and was treated with Propofol (View Usage). Patient experienced the following unwanted or unexpected effects: haematuria, post procedural complication, renal failure acute. Propofol dosage: Intravenous. During the same period patient was treated with ATRACURIUM (ATRACURIUM) (ATRACURIUM) (View Atracurium (atracurium) (atracurium) Review and Atracurium (atracurium) (atracurium) Label ), SUFENTA (SUFENTANIL CITRATE) (SUFENTANIL CITRATE) (View Sufenta (sufentanil Citrate) (sufentanil Citrate) Review and Sufenta (sufentanil Citrate) (sufentanil Citrate) Label ), NEURONTIN (View Neurontin Review and Neurontin Label ), BETADINE (POVIDONE IODINE) (POVIDONE IODINE) (View Betadine (povidone-iodine) (povidone-iodine) Review and Betadine (povidone-iodine) (povidone-iodine) Label ), NAROPEINE (ROPIVACAINE HYDROCHLORIDE) (ROPIVACAINE HYDROCHLORIDE) (View Naropeine (ropivacaine Hydrochloride) (ropivacaine Hydrochloride) Review and Naropeine (ropivacaine Hydrochloride) (ropivacaine Hydrochloride) Label ), DROLEPTAN (DROPERIDOL) (DROPERIDOL) (View Droleptan (droperidol) (droperidol) Review and Droleptan (droperidol) (droperidol) Label ), LOVENOX (HEPARIN FRACTION, SODIUM SALT0 (HEPARIN FRACTION, SODIUM SALT (View Lovenox (heparin-fraction, Sodium Salt0 (heparin-fraction, Sodium Salt Review and Lovenox (heparin-fraction, Sodium Salt0 (heparin-fraction, Sodium Salt Label ), KETAMINE (KETAMINE) (KETAMINE) (View Ketamine (ketamine) (ketamine) Review and Ketamine (ketamine) (ketamine) Label ). Patient was hospitalized.

6839882-2 | Haematuria, Haemolysis, Lymphopenia, Oliguria, Renal Failure Acute
Patient was taking Propofol (View Usage). Patient had the following side effects: haematuria, haemolysis, lymphopenia, oliguria, renal failure acute on Jun 18, 2010 from FRANCE Additional patient health information: Female patient , 40 years of age, was diagnosed with induction of anaesthesia and. Propofol dosage: Intravenous. During the same period patient was treated with ATRACURIUM (ATRACURIUM) (ATRACURIUM) (View Atracurium (atracurium) (atracurium) Review and Atracurium (atracurium) (atracurium) Label ), ULTIVA (REMIFENTANIL HYDROCHLORIDE) (REMIFENTANIL HYDROCHLORIDE) (View Ultiva (remifentanil Hydrochloride) (remifentanil Hydrochloride) Review and Ultiva (remifentanil Hydrochloride) (remifentanil Hydrochloride) Label ), NORMACOL LAVENT ADULTS (BACTRIM) (BACTRIM) (View Normacol Lavent Adults (bactrim) (bactrim) Review and Normacol Lavent Adults (bactrim) (bactrim) Label ), BETADINE (POVIDONE IODINE) (POVIDONE IODINE) (View Betadine (povidone-iodine) (povidone-iodine) Review and Betadine (povidone-iodine) (povidone-iodine) Label ), BETADINE DERMIQUE (POVIDONE IODINE) (POVIDONE IODINE) (View Betadine Dermique (povidone-iodine) (povidone-iodine) Review and Betadine Dermique (povidone-iodine) (povidone-iodine) Label ), AUGMENTIN (AUGMENTIN) (AUGMENTIN) (View Augmentin (augmentin) (augmentin) Review and Augmentin (augmentin) (augmentin) Label ), NEURONTINE (GABAPENTIN) (GABAPENTIN) (View Neurontine (gabapentin) (gabapentin) Review and Neurontine (gabapentin) (gabapentin) Label ), KETAMINE PANPHARMA (KETAMINE HYDROCHLORIDE) (KETAMINE HYDROCHLORIDE) (View Ketamine Panpharma (ketamine Hydrochloride) (ketamine Hydrochloride) Review and Ketamine Panpharma (ketamine Hydrochloride) (ketamine Hydrochloride) Label ). Patient was hospitalized.

6839880-9 | Lymphopenia, Post Procedural Complication, Renal Failure Acute, Renal Tubular Necrosis
Adverse event was reported on Jun 18, 2010 by a Female patient taking Propofol (View Usage) (Dosage: 800 Mg Intravenous) was diagnosed with induction of anaesthesia and. Location: FRANCE , 54 years of age, After Propofol was administered, patient had the following side effects: lymphopenia, post procedural complication, renal failure acute, renal tubular necrosis. During the same period patient was treated with ATRACURIUM HOSPIRA (ATRACURIUM) (ATRACURIUM) (View Atracurium Hospira (atracurium) (atracurium) Review and Atracurium Hospira (atracurium) (atracurium) Label ), ULTIVA (View Ultiva Review and Ultiva Label ), CLAMOXYL (AMOXICILLIN) (AMOXICILLIN) (View Clamoxyl (amoxicillin) (amoxicillin) Review and Clamoxyl (amoxicillin) (amoxicillin) Label ), METRONIDAZOLE MACO PHARMA (METRONIDAZOLE) (METRONIDAZOLE) (View Metronidazole Maco Pharma (metronidazole) (metronidazole) Review and Metronidazole Maco Pharma (metronidazole) (metronidazole) Label ), NORMACOL LAVEMENT ADULTES (BACTRIM) (BACTRIM) (View Normacol Lavement Adultes (bactrim) (bactrim) Review and Normacol Lavement Adultes (bactrim) (bactrim) Label ), MORPHINE LAVOISIRE (MORPHINE) (MORPHINE) (View Morphine Lavoisire (morphine) (morphine) Review and Morphine Lavoisire (morphine) (morphine) Label ), BETADINE DERMIQUE (POVIDONE IODINE) (POVIDONE IODINE) (View Betadine Dermique (povidone-iodine) (povidone-iodine) Review and Betadine Dermique (povidone-iodine) (povidone-iodine) Label ), NAROPEINE (ROPIVACAINE HYDROCHLORIDE) (ROPIVACAINE HYDROCHLORIDE) (View Naropeine (ropivacaine Hydrochloride) (ropivacaine Hydrochloride) Review and Naropeine (ropivacaine Hydrochloride) (ropivacaine Hydrochloride) Label ). Patient was hospitalized.

6837878-8 | Lymphopenia, Nephrolithiasis, Renal Failure Acute
on Jun 22, 2010 Female patient from FRANCE , 73 years of age, was diagnosed with induction of anaesthesia and was treated with Propofol (View Usage). Patient experienced the following unwanted or unexpected effects: lymphopenia, nephrolithiasis, renal failure acute. Propofol dosage: Intravenous. During the same period patient was treated with ATRACURIUM HOSPIRA (ATRACURIUM) (ATRACURIUM) (View Atracurium Hospira (atracurium) (atracurium) Review and Atracurium Hospira (atracurium) (atracurium) Label ), ULTIVA (REMIFENTANIL HYDROCHLORIDE) (REMIFENTANIL HYDROCHLORIDE) (View Ultiva (remifentanil Hydrochloride) (remifentanil Hydrochloride) Review and Ultiva (remifentanil Hydrochloride) (remifentanil Hydrochloride) Label ), NORMACOL LAVENT ADULTES (BACTRIM) (BACTRIM) (View Normacol Lavent Adultes (bactrim) (bactrim) Review and Normacol Lavent Adultes (bactrim) (bactrim) Label ), BETADINE DERMIQUE (POVIDONE IODINE) (POVIDONE IODINE) (View Betadine Dermique (povidone-iodine) (povidone-iodine) Review and Betadine Dermique (povidone-iodine) (povidone-iodine) Label ), AUGMENTIN (AUGMENTIN) (AUGMENTIN) (View Augmentin (augmentin) (augmentin) Review and Augmentin (augmentin) (augmentin) Label ), NEURONTINE (GABAPENTIN) (GABAPENTIN) (View Neurontine (gabapentin) (gabapentin) Review and Neurontine (gabapentin) (gabapentin) Label ), KETAMINE (KETAMINE) (KETAMINE) (View Ketamine (ketamine) (ketamine) Review and Ketamine (ketamine) (ketamine) Label ), NAROPEINE (ROPIVACAINE HYDROCHLORIDE) (ROPIVACAINE HYDROCHLORIDE) (View Naropeine (ropivacaine Hydrochloride) (ropivacaine Hydrochloride) Review and Naropeine (ropivacaine Hydrochloride) (ropivacaine Hydrochloride) Label ). Patient was hospitalized.


6837877-6 | Cardiac Failure, Condition Aggravated, Contrast Media Reaction, Diabetic Nephropathy, Dialysis, Hyperkalaemia, Oedema, Renal Failure Acute
on Jun 24, 2010 Male patient from GERMANY , 61 years of age, was treated with Propofol (View Usage). Patient had the following side effects: cardiac failure, condition aggravated, contrast media reaction, diabetic nephropathy, dialysis (What is dialysis?), hyperkalaemia, oedema, renal failure acute. Propofol dosage: 80 Mg. During the same period patient was treated with SPIRONOLACTON HEXAL (SPIRONOLACTONE) (SPIRONOLACTONE) (View Spironolacton Hexal (spironolactone) (spironolactone) Review and Spironolacton Hexal (spironolactone) (spironolactone) Label ).

6837875-2 | Condition Aggravated, Post Procedural Complication, Renal Failure Acute, Rheumatoid Arthritis
Patient was taking Propofol (View Usage). After Propofol was administered, patient had the following side effects: condition aggravated, post procedural complication, renal failure acute, rheumatoid arthritis (What is rheumatoid arthritis?) on Jun 22, 2010 from FRANCE Additional patient health information: Female patient , 78 years of age, was diagnosed with induction of anaesthesia and. Propofol dosage: Intravenous. During the same period patient was treated with SUFENTA (SUFENTANIL CITRATE) (SUFENTANIL CITRATE) (View Sufenta (sufentanil Citrate) (sufentanil Citrate) Review and Sufenta (sufentanil Citrate) (sufentanil Citrate) Label ), ATRACURIUM HOSPIRA (ATRACURIUM) (ATRACURIUM) (View Atracurium Hospira (atracurium) (atracurium) Review and Atracurium Hospira (atracurium) (atracurium) Label ), AUGMENTIN (AUGMENTIN) (AUGMENTIN) (View Augmentin (augmentin) (augmentin) Review and Augmentin (augmentin) (augmentin) Label ), SUPRANE (DESFLURANE) (DESFLURANE) (View Suprane (desflurane) (desflurane) Review and Suprane (desflurane) (desflurane) Label ), NAROPEINE (ROPIVACAINE HYDROCHLORIDE) (ROPIVACAINE HYDROCHLORIDE) (View Naropeine (ropivacaine Hydrochloride) (ropivacaine Hydrochloride) Review and Naropeine (ropivacaine Hydrochloride) (ropivacaine Hydrochloride) Label ), BETADINE DERMIQUE (POVIDONE IODINE) (POVIDONE IODINE) (View Betadine Dermique (povidone-iodine) (povidone-iodine) Review and Betadine Dermique (povidone-iodine) (povidone-iodine) Label ), NORMACOL LAVENT ADULTES (BACTRIM) (BACTRIM) (View Normacol Lavent Adultes (bactrim) (bactrim) Review and Normacol Lavent Adultes (bactrim) (bactrim) Label ), PERFALGAN (PARACETAMOL) (PARACETAMOL) (View Perfalgan (paracetamol) (paracetamol) Review and Perfalgan (paracetamol) (paracetamol) Label ). Patient was hospitalized.

6837872-7 | Lymphopenia, Renal Failure Acute, Thrombocytopenia
Adverse event was reported on Jun 23, 2010 by a Female patient taking Propofol (View Usage) (Dosage: ) was diagnosed with induction of anaesthesia and. Location: FRANCE , 36 years of age, Patient experienced the following unwanted or unexpected effects: lymphopenia, renal failure acute, thrombocytopenia. During the same period patient was treated with ULTIVA (View Ultiva Review and Ultiva Label ), NORMACOL (BACTRIM (BACTRIM) (View Normacol (bactrim (bactrim) Review and Normacol (bactrim (bactrim) Label ), BETADINE (POVIDONE IODINE) (POVIDONE IODINE) (View Betadine (povidone-iodine) (povidone-iodine) Review and Betadine (povidone-iodine) (povidone-iodine) Label ), NAROPEINE (ROPIVACAINEHYDROCHLORIDE) (ROPIVACAINE HYDROCHLORIDE) (View Naropeine (ropivacainehydrochloride) (ropivacaine Hydrochloride) Review and Naropeine (ropivacainehydrochloride) (ropivacaine Hydrochloride) Label ), DROPEPTAN (DROPERIDOL) (DROPERIDOL) (View Dropeptan (droperidol) (droperidol) Review and Dropeptan (droperidol) (droperidol) Label ), KETAMINE PANPHARMA (KETAMINE HYDROCHLORIDE) (KETAMINE HYDROCHLORIDE) (View Ketamine Panpharma (ketamine Hydrochloride) (ketamine Hydrochloride) Review and Ketamine Panpharma (ketamine Hydrochloride) (ketamine Hydrochloride) Label ), AUGMANTIN (AMOXI CLAVULANICO) (AMOXI CLAVULANICO) (View Augmantin (amoxi-clavulanico) (amoxi-clavulanico) Review and Augmantin (amoxi-clavulanico) (amoxi-clavulanico) Label ), MORPHIN LAVOISIER (MORPHINE) (MORPHINE) (View Morphin Lavoisier (morphine) (morphine) Review and Morphin Lavoisier (morphine) (morphine) Label ). Patient was hospitalized.

6832260-1 | Pancreatitis Acute
on Jul 09, 2010 Female patient from GERMANY , 73 years of age, weighting 154.3 lb, was diagnosed with uterine cervical erosion, postoperative analgesia and was treated with Propofol (View Usage). Patient had the following side effects: pancreatitis acute. Propofol dosage: . During the same period patient was treated with SUFENTANIL (View Sufentanil Review and Sufentanil Label ), BERLOSIN (View Berlosin Review and Berlosin Label ).

6832136-X | Lymphopenia, Post Procedural Complication, Renal Failure Acute
on Jun 23, 2010 Female patient from FRANCE , 34 years of age, was treated with Propofol (View Usage). After Propofol was administered, patient had the following side effects: lymphopenia, post procedural complication, renal failure acute. Propofol dosage: Intravenous (not Otherwise Specified). During the same period patient was treated with SUFENTA PRESERVATIVE FREE (View Sufenta Preservative Free Review and Sufenta Preservative Free Label ), NEURONTIN (View Neurontin Review and Neurontin Label ), NORMACOL LAVEMENT (BACTRIM) (View Normacol Lavement (bactrim) Review and Normacol Lavement (bactrim) Label ), DEXAMETASONE (View Dexametasone Review and Dexametasone Label ), EPHEDRINE (View Ephedrine Review and Ephedrine Label ), BETADINE DERMIQUE (POVIDONE IODINE) (View Betadine Dermique (povidone-iodine) Review and Betadine Dermique (povidone-iodine) Label ), NAROPEINE (ROPIVACAINE HYDROCHLORIDE) (View Naropeine (ropivacaine Hydrochloride) Review and Naropeine (ropivacaine Hydrochloride) Label ), DROPERIDOL (View Droperidol Review and Droperidol Label ). Patient was hospitalized.

6832126-7 | Renal Failure Acute
Patient was taking Propofol (View Usage). Patient experienced the following unwanted or unexpected effects: renal failure acute on Jun 16, 2010 from FRANCE Additional patient health information: Female patient , 49 years of age, was diagnosed with induction of anaesthesia and. Propofol dosage: Intravenous (not Otherwise Specified). During the same period patient was treated with ATRACURIUM (View Atracurium Review and Atracurium Label ), SUFENTA PRESERVATIVE FREE (View Sufenta Preservative Free Review and Sufenta Preservative Free Label ), NORMACOL (BACTRIM) (View Normacol (bactrim) Review and Normacol (bactrim) Label ), DEXAMETHASON MERCK (DEXAMETHASONE SODIUM PHOSPHATE) (View Dexamethason Merck (dexamethasone Sodium Phosphate) Review and Dexamethason Merck (dexamethasone Sodium Phosphate) Label ), ACUPAN (View Acupan Review and Acupan Label ), BETADINE (View Betadine Review and Betadine Label ), NAROPEINE (ROPIVACAINE HYDROCHLORIDE) (View Naropeine (ropivacaine Hydrochloride) Review and Naropeine (ropivacaine Hydrochloride) Label ), DROPERIDOL (View Droperidol Review and Droperidol Label ). Patient was hospitalized.

6832124-3 | Acute Pulmonary Oedema, Continuous Haemodiafiltration, Fluid Overload, Metabolic Acidosis, Pleural Effusion, Renal Failure Acute
Adverse event was reported on Jun 23, 2010 by a Female patient taking Propofol (View Usage) (Dosage: ) was diagnosed with induction of anaesthesia and. Location: GERMANY , 47 years of age, Patient had the following side effects: acute pulmonary oedema, continuous haemodiafiltration, fluid overload, metabolic acidosis, pleural effusion, renal failure acute. During the same period patient was treated with SUFENTA (SUFENTANILCITRATE) (SUFENTANIL CITRATE) (View Sufenta (sufentanilcitrate) (sufentanil Citrate) Review and Sufenta (sufentanilcitrate) (sufentanil Citrate) Label ), ATRACURIUM (ATRACURIUM) (ATRACURIUM) (View Atracurium (atracurium) (atracurium) Review and Atracurium (atracurium) (atracurium) Label ), AUGMANTIN (AMOXI CLAVULANICO) (AMOXI CLAVULANICO) (View Augmantin (amoxi-clavulanico) (amoxi-clavulanico) Review and Augmantin (amoxi-clavulanico) (amoxi-clavulanico) Label ), KETAMIN (KETAMINE HYDROCHLORIDE) (KETAMINE HYDROCHLORIDE) (View Ketamin (ketamine Hydrochloride) (ketamine Hydrochloride) Review and Ketamin (ketamine Hydrochloride) (ketamine Hydrochloride) Label ), SUPRANE (DEFLURANE) (DESFLURANE) (View Suprane (deflurane) (desflurane) Review and Suprane (deflurane) (desflurane) Label ), NAROPEINE (ROPIVACAINE HYDROCHLORIDE) (ROPIVACAINE HYDROCHLORIDE) (View Naropeine (ropivacaine Hydrochloride) (ropivacaine Hydrochloride) Review and Naropeine (ropivacaine Hydrochloride) (ropivacaine Hydrochloride) Label ), NEURONTIN (View Neurontin Review and Neurontin Label ), BETADIN (POVIDONE IODINE) (POVIDONE IODINE) (View Betadin (povidone-iodine) (povidone-iodine) Review and Betadin (povidone-iodine) (povidone-iodine) Label ). Patient was hospitalized.

6826795-5 | Agitation, Circulatory Collapse, Hyperkalaemia, Hypotension, Metabolic Acidosis, Propofol Infusion Syndrome, Renal Failure
on Jun 28, 2010 Male patient from CANADA , 22 years of age, was treated with Propofol (View Usage). After Propofol was administered, patient had the following side effects: agitation, circulatory collapse, hyperkalaemia, hypotension, metabolic acidosis, propofol infusion syndrome, renal failure. Propofol dosage: 90-100ug/kg/minute. During the same period patient was treated with FENTANYL (View Fentanyl Review and Fentanyl Label ).

6818770-1 | Cerebrovascular Accident, Loss Of Consciousness
on Jun 21, 2010 Female patient from UNITED STATES , 20 years of age, was diagnosed with anaesthesia and was treated with Propofol (View Usage). Patient experienced the following unwanted or unexpected effects: cerebrovascular accident, loss of consciousness. Propofol dosage: . Patient was hospitalized.

6818752-X | Haematuria, Haemolysis, Lymphopenia, Oliguria, Renal Failure Acute
Patient was taking Propofol (View Usage). Patient had the following side effects: haematuria, haemolysis, lymphopenia, oliguria, renal failure acute on Jun 18, 2010 from FRANCE Additional patient health information: Female patient , 46 years of age, was diagnosed with induction of anaesthesia and. Propofol dosage: Intravenous. During the same period patient was treated with ATRACURIUM (ATRACURIUM) (ATRACURIUM) (View Atracurium (atracurium) (atracurium) Review and Atracurium (atracurium) (atracurium) Label ), SUFENTA (SUFENTANIL CITRATE) (SUFENTANIL CITRATE) (View Sufenta (sufentanil Citrate) (sufentanil Citrate) Review and Sufenta (sufentanil Citrate) (sufentanil Citrate) Label ), NORMACOL (BACTRIM) (BACTRIM) (View Normacol (bactrim) (bactrim) Review and Normacol (bactrim) (bactrim) Label ), DROLEPTAN (DROPERIDOL) (DROPERIDOL) (View Droleptan (droperidol) (droperidol) Review and Droleptan (droperidol) (droperidol) Label ), AUGMENTIN (AMOXICILLIN W/CALVULANATE POTASSIUM) (AMOXICILLIN W/CLAVULA (View Augmentin (amoxicillin W/calvulanate Potassium) (amoxicillin W/clavula Review and Augmentin (amoxicillin W/calvulanate Potassium) (amoxicillin W/clavula Label ), SEVORANE (SEVOFLURANE) (SEVOFLURANE) (View Sevorane (sevoflurane) (sevoflurane) Review and Sevorane (sevoflurane) (sevoflurane) Label ), KALINOX (ENTONOX) (ENTONOX) (View Kalinox (entonox) (entonox) Review and Kalinox (entonox) (entonox) Label ). Patient was hospitalized.

6812232-3 | Ischaemia, Penile Vascular Disorder
Adverse event was reported on Jun 28, 2010 by a Male patient taking Propofol (View Usage) (Dosage: ) was diagnosed with induction of anaesthesia, endotracheal intubation, epidural anaesthesia, maintenance of anaesthesia and. Location: UNITED KINGDOM , child 4 years of age, weighting 33.07 lb, After Propofol was administered, patient had the following side effects: ischaemia, penile vascular disorder. During the same period patient was treated with ATRACURIUM (View Atracurium Review and Atracurium Label ), CLONIDINE (View Clonidine Review and Clonidine Label ), LEVOBUPIVACAINE (View Levobupivacaine Review and Levobupivacaine Label ), ACETAMINOPHEN (View Acetaminophen Review and Acetaminophen Label ), SEVOFLURANE (View Sevoflurane Review and Sevoflurane Label ).

6812067-1 | Lymphopenia, Renal Failure Acute
on Jun 09, 2010 Female patient from FRANCE , 36 years of age, was diagnosed with induction of anaesthesia and was treated with Propofol (View Usage). Patient experienced the following unwanted or unexpected effects: lymphopenia, renal failure acute. Propofol dosage: . During the same period patient was treated with ATRACURIUM HOSPIRA (ATRACURIUM) (ATRACURIUM) (View Atracurium Hospira (atracurium) (atracurium) Review and Atracurium Hospira (atracurium) (atracurium) Label ), ULTIVA (REMIFENTANIL HYDROCHLORIDE) (REMIFENTANIL HYDROCHLORIDE) (View Ultiva (remifentanil Hydrochloride) (remifentanil Hydrochloride) Review and Ultiva (remifentanil Hydrochloride) (remifentanil Hydrochloride) Label ), NORMACOL (BACTRIM) (BACTRIM) (View Normacol (bactrim) (bactrim) Review and Normacol (bactrim) (bactrim) Label ), BETADINE (POVIDONE IODINE) (POVIDONE IODINE) (View Betadine (povidone-iodine) (povidone-iodine) Review and Betadine (povidone-iodine) (povidone-iodine) Label ), NAROPEINE (ROPIVACAINE HYDROCHLORIDE) (ROPIVACAINE HYDROCHLORIDE) (View Naropeine (ropivacaine Hydrochloride) (ropivacaine Hydrochloride) Review and Naropeine (ropivacaine Hydrochloride) (ropivacaine Hydrochloride) Label ), DROPEPTAN (DROPERIDOL) (DROPERIDOL) (View Dropeptan (droperidol) (droperidol) Review and Dropeptan (droperidol) (droperidol) Label ), KETAMINE PANPHARMA (KETAMINE HYDROCHLORIDE) (KETAMINE HYDROCHLORIDE) (View Ketamine Panpharma (ketamine Hydrochloride) (ketamine Hydrochloride) Review and Ketamine Panpharma (ketamine Hydrochloride) (ketamine Hydrochloride) Label ), AUGMANTIN (AMOXI CLAVULANICO) (AMOXI CLAVULANICO) (View Augmantin (amoxi-clavulanico) (amoxi-clavulanico) Review and Augmantin (amoxi-clavulanico) (amoxi-clavulanico) Label ). Patient was hospitalized.

6812065-8 | Acute Pulmonary Oedema, Renal Failure Acute
on Jun 09, 2010 Female patient from FRANCE , 47 years of age, was diagnosed with induction of anaesthesia and was treated with Propofol (View Usage). Patient had the following side effects: acute pulmonary oedema, renal failure acute. Propofol dosage: . During the same period patient was treated with SUFENTA (SUFENTANIL CITRATE) (SUFENTANIL CITRATE) (View Sufenta (sufentanil Citrate) (sufentanil Citrate) Review and Sufenta (sufentanil Citrate) (sufentanil Citrate) Label ), ATRACURIUM (ATRACURIUM) (ATRACURIUM) (View Atracurium (atracurium) (atracurium) Review and Atracurium (atracurium) (atracurium) Label ), KETAMIN (KETAMINE HYDROCHLORIDE) (KETAMINE HYDROCHLORIDE) (View Ketamin (ketamine Hydrochloride) (ketamine Hydrochloride) Review and Ketamin (ketamine Hydrochloride) (ketamine Hydrochloride) Label ), SUPRANE (View Suprane Review and Suprane Label ), NORAPEINE (ROPIVACAINE HYDROCHLORIDE) (ROPIVACINE HYDROCHLORIDE) (View Norapeine (ropivacaine Hydrochloride) (ropivacine Hydrochloride) Review and Norapeine (ropivacaine Hydrochloride) (ropivacine Hydrochloride) Label ), NEURONTIN (View Neurontin Review and Neurontin Label ), BETADIN (POVIDONE IODINE) (PROVIDONE IODINE) (View Betadin (povidone-iodine) (providone-iodine) Review and Betadin (povidone-iodine) (providone-iodine) Label ), NORMACOL (NORMACOL) (NORMACOL) (View Normacol (normacol) (normacol) Review and Normacol (normacol) (normacol) Label ). Patient was hospitalized.

6812061-0 | Lymphopenia, Renal Failure Acute
Patient was taking Propofol (View Usage). After Propofol was administered, patient had the following side effects: lymphopenia, renal failure acute on Jun 09, 2010 from FRANCE Additional patient health information: Female patient , 34 years of age, was diagnosed with induction of anaesthesia and. Propofol dosage: . During the same period patient was treated with SUFENTA (SUFENTANIL CITRATE) (SUFENTANIL CITRATE) (View Sufenta (sufentanil Citrate) (sufentanil Citrate) Review and Sufenta (sufentanil Citrate) (sufentanil Citrate) Label ), NEURONTIN (View Neurontin Review and Neurontin Label ), NORMACOL LAVEMENT (BACTRIM) (BACTRIM) (View Normacol Lavement (bactrim) (bactrim) Review and Normacol Lavement (bactrim) (bactrim) Label ), DEXAMETHASONE (View Dexamethasone Review and Dexamethasone Label ), EPHEDRINE (EPHEDRINE) (EPHEDRINE) (View Ephedrine (ephedrine) (ephedrine) Review and Ephedrine (ephedrine) (ephedrine) Label ), BETADINE DERMIQUE (POVIDONE IODINE) (POVIDONE IODINE) (View Betadine Dermique (povidone-iodine) (povidone-iodine) Review and Betadine Dermique (povidone-iodine) (povidone-iodine) Label ), NAROPEINE (ROPIVACAINE HYDROCHLORIDE) (ROPIVACAINE HYDROCHLORIDE) (View Naropeine (ropivacaine Hydrochloride) (ropivacaine Hydrochloride) Review and Naropeine (ropivacaine Hydrochloride) (ropivacaine Hydrochloride) Label ), DROLEPTAN (DROPERIDOL) (DROPERIDOL) (View Droleptan (droperidol) (droperidol) Review and Droleptan (droperidol) (droperidol) Label ). Patient was hospitalized.

6801309-4 | Abdominal Pain, Anaemia, Arteriovenous Fistula Thrombosis, Aspiration, Blood Pressure Decreased, Blood Pressure Fluctuation, Chest Pain, Confusional State, Diarrhoea
Adverse event was reported on Jun 18, 2010 by a Male patient taking Propofol (View Usage) (Dosage: ) was diagnosed with thrombectomy, arteriovenous fistula operation and. Location: UNITED STATES , weighting 175.2 lb, Patient experienced the following unwanted or unexpected effects: abdominal pain (What is abdominal pain?), anaemia, arteriovenous fistula thrombosis, aspiration, blood pressure decreased, blood pressure fluctuation, chest pain (What is chest pain?), confusional state, diarrhoea. During the same period patient was treated with HEPARIN SODIUM (View Heparin Sodium Review and Heparin Sodium Label ), MORNIFLUMATE (View Morniflumate Review and Morniflumate Label ), ROSUVASTATIN (View Rosuvastatin Review and Rosuvastatin Label ), VENLAFAXINE (View Venlafaxine Review and Venlafaxine Label ), GABAPENTIN (View Gabapentin Review and Gabapentin Label ), EZETIMIBE (View Ezetimibe Review and Ezetimibe Label ). Patient was hospitalized.

6800686-8 | Bradycardia, Cerebral Ischaemia, Hypotension, Hypoxia, Post Procedural Complication
on Jun 07, 2010 Male patient from UNITED STATES , 68 years of age, weighting 226.5 lb, was treated with Propofol (View Usage). Patient had the following side effects: bradycardia, cerebral ischaemia, hypotension, hypoxia, post procedural complication. Propofol dosage: 130 Mg, Once, Intravenous.

6796356-5 | Cerebrovascular Accident, Loss Of Consciousness
on Jun 08, 2010 Female patient from CANADA , 20 years of age, was diagnosed with anaesthesia and was treated with Propofol (View Usage). After Propofol was administered, patient had the following side effects: cerebrovascular accident, loss of consciousness. Propofol dosage: . Patient was hospitalized.

6782230-7 | Haematuria, Lymphopenia, Oliguria, Post Procedural Complication, Renal Failure Acute
Patient was taking Propofol (View Usage). Patient experienced the following unwanted or unexpected effects: haematuria, lymphopenia, oliguria, post procedural complication, renal failure acute on Jun 02, 2010 from FRANCE Additional patient health information: Female patient , 54 years of age, was diagnosed with induction of anaesthesia and. Propofol dosage: 800 Mg, Intravenous. During the same period patient was treated with ATRACURIUM HOSPIRA (ATRACURIUM) (ATRUCURIUM) (View Atracurium Hospira (atracurium) (atrucurium) Review and Atracurium Hospira (atracurium) (atrucurium) Label ), ULTIVA (REMIFENTANIL HYDROCHLORIDE) (REMIFENTANYL HYDROCHLORIDE) (View Ultiva (remifentanil Hydrochloride) (remifentanyl Hydrochloride) Review and Ultiva (remifentanil Hydrochloride) (remifentanyl Hydrochloride) Label ), CLAMOXYL (AMOXICILLIN) (AMOXICILLIN) (View Clamoxyl (amoxicillin) (amoxicillin) Review and Clamoxyl (amoxicillin) (amoxicillin) Label ), METRONIDAZOLE MACO PHARMA (METRONIDAZOLE) (METRONIDAZOLE) (View Metronidazole Maco Pharma (metronidazole) (metronidazole) Review and Metronidazole Maco Pharma (metronidazole) (metronidazole) Label ), NORMACOL LAVEMENT ADULTES (BACTRIM) (BACTRIM) (View Normacol Lavement Adultes (bactrim) (bactrim) Review and Normacol Lavement Adultes (bactrim) (bactrim) Label ), MORPHINE LAVOISIRE (MORPHINE) (MORPHINE) (View Morphine Lavoisire (morphine) (morphine) Review and Morphine Lavoisire (morphine) (morphine) Label ), BETADINE DERMIQUE (POVIDONE IODINE) (POVIDONE IODINE) (View Betadine Dermique (povidone-iodine) (povidone-iodine) Review and Betadine Dermique (povidone-iodine) (povidone-iodine) Label ), NAROPEINE (ROPIVACAINE HYDROCHLORIDE) (ROPIVACAINE HYDROCHLORIDE) (View Naropeine (ropivacaine Hydrochloride) (ropivacaine Hydrochloride) Review and Naropeine (ropivacaine Hydrochloride) (ropivacaine Hydrochloride) Label ). Patient was hospitalized.

6782209-5 | Eosinophil Count Abnormal, Renal Failure Acute, White Blood Cell Count Abnormal
Adverse event was reported on Jun 08, 2010 by a Female patient taking Propofol (View Usage) (Dosage: Intravenous) was diagnosed with induction of anaesthesia and. Location: FRANCE , 51 years of age, Patient had the following side effects: eosinophil count abnormal, renal failure acute, white blood cell count abnormal. During the same period patient was treated with SUFENTA (SUFENTANIL CITRATE( (SUFENTANIL CITRATE) (View Sufenta (sufentanil Citrate( (sufentanil Citrate) Review and Sufenta (sufentanil Citrate( (sufentanil Citrate) Label ), ATRACURIUM (ATRACURIUM) (ATRACURIUM) (View Atracurium (atracurium) (atracurium) Review and Atracurium (atracurium) (atracurium) Label ), AUGMENTIN (AUGMENTIN) (AUGMENTIN) (View Augmentin (augmentin) (augmentin) Review and Augmentin (augmentin) (augmentin) Label ), KETAMINE PANPHARMA (KETAMINE HYDROCHLORIDE) (KETAMINE HYDROCHLORIDE) (View Ketamine Panpharma (ketamine Hydrochloride) (ketamine Hydrochloride) Review and Ketamine Panpharma (ketamine Hydrochloride) (ketamine Hydrochloride) Label ), NICARDIPINE AUGUETTANT (NICARDIPINE HYDROCHLORIDE) (NICARDIPINE HYDROC (View Nicardipine Auguettant (nicardipine Hydrochloride) (nicardipine Hydroc Review and Nicardipine Auguettant (nicardipine Hydrochloride) (nicardipine Hydroc Label ), SEVORANE (SEVOFLURANE) (SEVOFLURANE) (View Sevorane (sevoflurane) (sevoflurane) Review and Sevorane (sevoflurane) (sevoflurane) Label ), DROLEPTAN (DROPERIDOL) (DROPERIDOL) (View Droleptan (droperidol) (droperidol) Review and Droleptan (droperidol) (droperidol) Label ), NAROPEINE (ROPIVACAINE HYDROCHLORIDE) (ROPIVACAINE HYDROCHLORIDE) (View Naropeine (ropivacaine Hydrochloride) (ropivacaine Hydrochloride) Review and Naropeine (ropivacaine Hydrochloride) (ropivacaine Hydrochloride) Label ). Patient was hospitalized.

6782206-X | Bradycardia, Cardiac Arrest, Depressed Level Of Consciousness, Hyperkalaemia, Hypocalcaemia, Respiratory Arrest, Rhabdomyolysis
on Jun 07, 2010 Male patient from UNITED KINGDOM , child 12 years of age, was diagnosed with induction of anaesthesia and was treated with Propofol (View Usage). After Propofol was administered, patient had the following side effects: bradycardia, cardiac arrest (What is cardiac arrest?), depressed level of consciousness, hyperkalaemia, hypocalcaemia, respiratory arrest, rhabdomyolysis. Propofol dosage: 150 Mg Intravenous. During the same period patient was treated with FENTANYL (View Fentanyl Review and Fentanyl Label ), ISOFLURANE (ISOFLURANE) (ISOFLURANE) (View Isoflurane (isoflurane) (isoflurane) Review and Isoflurane (isoflurane) (isoflurane) Label ).

6781237-3 | Blood Creatine Phosphokinase Increased, Hepatocellular Injury, Hypertriglyceridaemia, Intracranial Pressure Increased, Renal Failure Acute
on Jun 16, 2010 Male patient from SWITZERLAND , 16 years of age, was diagnosed with sedation and was treated with Propofol (View Usage). Patient experienced the following unwanted or unexpected effects: blood creatine phosphokinase increased, hepatocellular injury, hypertriglyceridaemia, intracranial pressure increased, renal failure acute. Propofol dosage: . During the same period patient was treated with SINTENYL (View Sintenyl Review and Sintenyl Label ), DORMICUM (View Dormicum Review and Dormicum Label ), PANTOTHAL (400 Mg Total) (View Pantothal Review and Pantothal Label ).

6781041-6 | Off Label Use, Propofol Infusion Syndrome
Patient was taking Propofol (View Usage). Patient had the following side effects: off label use, propofol infusion syndrome on Jun 16, 2010 from FRANCE Additional patient health information: Female patient , 17 years of age, weighting 112.4 lb, was diagnosed with convulsion, sedation and. Propofol dosage: During The First 4 Hour 100 Mg Bolus Propofol Was Progressively Increased Up To 400 Mg.

6777832-8 | Catatonia, Neuroleptic Malignant Syndrome
Adverse event was reported on Jun 03, 2010 by a Female patient taking Propofol (View Usage) (Dosage: ) was diagnosed with pain (What is pain?), anxiety (What is anxiety?) and. Location: JAPAN , 18 years of age, weighting 110.2 lb, After Propofol was administered, patient had the following side effects: catatonia, neuroleptic malignant syndrome. During the same period patient was treated with FENTANYL (View Fentanyl Review and Fentanyl Label ), DROPERIDOL (1ml: In 50ml Solution, Infused At 1 Ml/hour) (View Droperidol Review and Droperidol Label ), HALOPERIDOL (View Haloperidol Review and Haloperidol Label ), ROPIVACAINE HYDROCHLORIDE (10ml; In 50ml Solution, Infused At 1 Ml/hour) (View Ropivacaine Hydrochloride Review and Ropivacaine Hydrochloride Label ), MORPHINE (1ml; In 50ml Solution, Infused At 1 Ml/hour) (View Morphine Review and Morphine Label ), SODIUM CHLORIDE (In 50ml Solution, Infused At 1 Ml/hour) (View Sodium Chloride Review and Sodium Chloride Label ). Patient was hospitalized.

6767424-9 | Bradycardia, Hypotension, Hypoxia
on Jun 11, 2010 Male patient from UNITED STATES , 69 years of age, weighting 226.0 lb, was diagnosed with oesophagogastroduodenoscopy, sedation and was treated with Propofol (View Usage). Patient experienced the following unwanted or unexpected effects: bradycardia, hypotension, hypoxia. Propofol dosage: 130 Mg X1 Dose Iv.

6767322-0 | Abdominal Pain Upper, Product Contamination, Product Quality Issue
on Jun 11, 2010 Male patient from UNITED STATES , weighting 169.0 lb, was diagnosed with tracheostomy and was treated with Propofol (View Usage). Patient had the following side effects: abdominal pain upper, product contamination, product quality issue. Propofol dosage: . Patient was hospitalized.

6766133-X | Blood Lactate Dehydrogenase Increased, Nephrolithiasis, Post Procedural Haematuria, Renal Failure Acute
Patient was taking Propofol (View Usage). After Propofol was administered, patient had the following side effects: blood lactate dehydrogenase increased, nephrolithiasis, post procedural haematuria, renal failure acute on May 27, 2010 from FRANCE Additional patient health information: Female patient , 60 years of age, was diagnosed with anaesthesia and. Propofol dosage: . During the same period patient was treated with AUGMENTAN (AUGMENTIN) (AUGMENTIN) (View Augmentan (augmentin) (augmentin) Review and Augmentan (augmentin) (augmentin) Label ), ATRACURIUM (ATRACURIUM) (ATRACURIUM) (View Atracurium (atracurium) (atracurium) Review and Atracurium (atracurium) (atracurium) Label ), ULTIVA (REMIFENTANIL HYDROCHLORIDE) (REMIFENTANIL HYDROCHLORIDE) (View Ultiva (remifentanil Hydrochloride) (remifentanil Hydrochloride) Review and Ultiva (remifentanil Hydrochloride) (remifentanil Hydrochloride) Label ), KETAMINE PANPHARMA (KETAMINE HYDROCHLORIDE) (KETAMINE HYDROCHLORIDE) (View Ketamine Panpharma (ketamine Hydrochloride) (ketamine Hydrochloride) Review and Ketamine Panpharma (ketamine Hydrochloride) (ketamine Hydrochloride) Label ), DROLEPTAN (DROPERIDOL) (DROPERIDOL0 (View Droleptan (droperidol) (droperidol0 Review and Droleptan (droperidol) (droperidol0 Label ), NEURONTIN (View Neurontin Review and Neurontin Label ), BETADINE (POVIDONE IODINE) (POVIDONE IODINE) (View Betadine (povidone-iodine) (povidone-iodine) Review and Betadine (povidone-iodine) (povidone-iodine) Label ). Patient was hospitalized.

6764060-5 | Renal Failure Acute
Adverse event was reported on May 27, 2010 by a Female patient taking Propofol (View Usage) (Dosage: Intravenous (not Otherwise Specified)) was diagnosed with induction of anaesthesia and. Location: FRANCE , 51 years of age, Patient experienced the following unwanted or unexpected effects: renal failure acute. During the same period patient was treated with SUFENTA PRESERVATIVE FREE (View Sufenta Preservative Free Review and Sufenta Preservative Free Label ), ATRACURIUM (View Atracurium Review and Atracurium Label ), AUGMENTIN '125' (View Augmentin '125' Review and Augmentin '125' Label ), KETAMINE PANPHARMA (KETAMINE HYDROCHLORIDE) (View Ketamine Panpharma (ketamine Hydrochloride) Review and Ketamine Panpharma (ketamine Hydrochloride) Label ), NICARDIPINE AUGUETTANT (NICARDIPINE HYDROCHLORIDE) (View Nicardipine Auguettant (nicardipine Hydrochloride) Review and Nicardipine Auguettant (nicardipine Hydrochloride) Label ), SEVOFLURANE (View Sevoflurane Review and Sevoflurane Label ), DROPERIDOL (View Droperidol Review and Droperidol Label ), NAROPEINE (ROPIVACAINE HYDROCHLORIDE) (View Naropeine (ropivacaine Hydrochloride) Review and Naropeine (ropivacaine Hydrochloride) Label ). Patient was hospitalized.

6763868-X | Tonic Convulsion
on Jun 03, 2010 Female patient from GERMANY , 50 years of age, weighting 154.3 lb, was treated with Propofol (View Usage). Patient had the following side effects: tonic convulsion. Propofol dosage: .

6758586-8 | Hypoxia, Muscle Rigidity, Mydriasis, Psychomotor Hyperactivity
on Apr 19, 2010 Male patient from SPAIN , 59 years of age, was diagnosed with induction of anaesthesia and was treated with Propofol (View Usage). After Propofol was administered, patient had the following side effects: hypoxia, muscle rigidity, mydriasis, psychomotor hyperactivity. Propofol dosage: .

6757784-7 | Cellulitis, Infusion Site Erythema, Injected Limb Mobility Decreased, Musculoskeletal Stiffness, Pain In Extremity, Product Quality Issue
Patient was taking Propofol (View Usage). Patient experienced the following unwanted or unexpected effects: cellulitis (What is cellulitis?), infusion site erythema, injected limb mobility decreased, musculoskeletal stiffness, pain in extremity, product quality issue on Jun 04, 2010 from UNITED STATES Additional patient health information: Female patient , 39 years of age, weighting 113.0 lb, . Propofol dosage: 140 Mg 2 X Over 15 Minute Iv Bolus. Patient was hospitalized and became disabled.

6755427-X | Becker's Muscular Dystrophy, Bradycardia, Cardiac Arrest, Depressed Level Of Consciousness, Hyperkalaemia, Hypocalcaemia, Hypoxia, Respiratory Arrest, Rhabdomyolysis
Adverse event was reported on May 28, 2010 by a Male patient taking Propofol (View Usage) (Dosage: ) was diagnosed with anaesthesia and. Location: UNITED KINGDOM , child 12 years of age, weighting 116.8 lb, Patient had the following side effects: becker's muscular dystrophy, bradycardia, cardiac arrest (What is cardiac arrest?), depressed level of consciousness, hyperkalaemia, hypocalcaemia, hypoxia, respiratory arrest, rhabdomyolysis. During the same period patient was treated with FENTANYL (View Fentanyl Review and Fentanyl Label ), ISOFLURANE (View Isoflurane Review and Isoflurane Label ).

6752524-X | Abnormal Behaviour, Aggression, Psychotic Disorder
on May 17, 2010 Female patient from UNITED STATES , 29 years of age, was diagnosed with induction of anaesthesia and was treated with Propofol (View Usage). After Propofol was administered, patient had the following side effects: abnormal behaviour, aggression, psychotic disorder (What is psychotic disorder?). Propofol dosage: 120 Mg Milligram (s), Intravenous. During the same period patient was treated with FENTANYL CITRATE (View Fentanyl Citrate Review and Fentanyl Citrate Label ), NITROUS (OXIDE) (View Nitrous (oxide) Review and Nitrous (oxide) Label ).

6752135-6 | Cerebrovascular Accident, Deep Vein Thrombosis, Electrocardiogram Abnormal, Infusion Site Pain, Infusion Site Phlebitis, Transient Ischaemic Attack
on Jun 01, 2010 Male patient from UNITED STATES , 54 years of age, weighting 180.0 lb, was diagnosed with anaesthesia and was treated with Propofol (View Usage). Patient experienced the following unwanted or unexpected effects: cerebrovascular accident, deep vein thrombosis (What is deep vein thrombosis?), electrocardiogram abnormal, infusion site pain, infusion site phlebitis, transient ischaemic attack. Propofol dosage: .

6741287-X | Pulmonary Embolism
Patient was taking Propofol (View Usage). Patient had the following side effects: pulmonary embolism (What is pulmonary embolism?) on May 05, 2010 from GERMANY Additional patient health information: Female patient , 75 years of age, . Propofol dosage: . During the same period patient was treated with SOBRIL (View Sobril Review and Sobril Label ), EDRONAX (View Edronax Review and Edronax Label ), CURACIT (View Curacit Review and Curacit Label ), NORTRIPTYLINE HCL (View Nortriptyline Hcl Review and Nortriptyline Hcl Label ), SINEMET (25/100) (View Sinemet Review and Sinemet Label ), FLUTIDE (View Flutide Review and Flutide Label ), ATROPIN (View Atropin Review and Atropin Label ). Patient was hospitalized.

6729640-1 | Acidosis, Electrocardiogram St Segment Elevation, Hypotension, Hypothermia, Renal Failure Acute, Rhabdomyolysis, Unresponsive To Stimuli
Adverse event was reported on May 03, 2010 by a Male patient taking Propofol (View Usage) (Dosage: 20 Mcg/kg/min, Intravenous) . Location: UNITED STATES , 21 years of age, After Propofol was administered, patient had the following side effects: acidosis, electrocardiogram st segment elevation, hypotension, hypothermia (What is hypothermia?), renal failure acute, rhabdomyolysis, unresponsive to stimuli. During the same period patient was treated with DOPAMINE HYDROCHLORIDE (View Dopamine Hydrochloride Review and Dopamine Hydrochloride Label ), ... (View ... Review and ... Label ). Patient was hospitalized.

6722724-3 | Acute Respiratory Distress Syndrome, Bacteroides Infection, Enterobacter Infection, Haemodialysis, Pleural Effusion, Renal Failure, Septic Shock, Skin Lesion
on Apr 22, 2010 Female patient from NETHERLANDS , 47 years of age, was treated with Propofol (View Usage). Patient experienced the following unwanted or unexpected effects: acute respiratory distress syndrome, bacteroides infection, enterobacter infection, haemodialysis, pleural effusion, renal failure, septic shock, skin lesion. Propofol dosage: Intravenous. During the same period patient was treated with (HUMAN ACTRAPID) (View (human Actrapid) Review and (human Actrapid) Label ), MIDAZOLAM HCL (1 Mg Milligram(s), Intravenous) (View Midazolam Hcl Review and Midazolam Hcl Label ), LOVENOX (Subcutaneous) (View Lovenox Review and Lovenox Label ), AMOXICILLIN AND CLAVULANATE POTASSIUM (Intravenous) (View Amoxicillin And Clavulanate Potassium Review and Amoxicillin And Clavulanate Potassium Label ), (MOPRAL /00661201/) (40 Mg Milligram(s), Intravenous) (View (mopral /00661201/) Review and (mopral /00661201/) Label ), CANCIDAS (50 Mg Milligram(s), Intravenous) (View Cancidas Review and Cancidas Label ), SUFENTA PRESERVATIVE FREE (Intravenous) (View Sufenta Preservative Free Review and Sufenta Preservative Free Label ), (VECTARION) (Intravenous) (View (vectarion) Review and (vectarion) Label ). Patient was hospitalized.

6721151-2 | Arteriospasm Coronary, Hypotension, Prinzmetal Angina
on Apr 22, 2010 Female patient from TURKEY , 68 years of age, was diagnosed with induction of anaesthesia and was treated with Propofol (View Usage). Patient had the following side effects: arteriospasm coronary, hypotension, prinzmetal angina. Propofol dosage: 140 Mg. During the same period patient was treated with FENTANYL (View Fentanyl Review and Fentanyl Label ), VECURONIUM BROMIDE (View Vecuronium Bromide Review and Vecuronium Bromide Label ).

6715441-7 | Cardiac Failure Acute
Patient was taking Propofol (View Usage). After Propofol was administered, patient had the following side effects: cardiac failure acute on May 04, 2010 from UNITED STATES Additional patient health information: Female patient , 19 years of age, weighting 154.3 lb, was diagnosed with induction of anaesthesia and. Propofol dosage: . During the same period patient was treated with FENTANYL (View Fentanyl Review and Fentanyl Label ), MIDAZOLAM HCL (View Midazolam Hcl Review and Midazolam Hcl Label ), SEVOFLURANE (View Sevoflurane Review and Sevoflurane Label ), SUCCINYLCHOLINE (60 Mgx1) (View Succinylcholine Review and Succinylcholine Label ).

6710026-0 | Hyperthermia Malignant
Adverse event was reported on Apr 22, 2010 by a Female patient taking Propofol (View Usage) (Dosage: Intravenous) was diagnosed with dental care and. Location: UNITED STATES , child 5 years of age, weighting 38.74 lb, Patient experienced the following unwanted or unexpected effects: hyperthermia malignant. During the same period patient was treated with ULTANE (Inhalation) (View Ultane Review and Ultane Label ), CEFAZOLIN SODIUM (View Cefazolin Sodium Review and Cefazolin Sodium Label ), FENTANYL 100 (View Fentanyl-100 Review and Fentanyl-100 Label ).

6706922-0 | Blood Triglycerides Increased
on Apr 30, 2010 Male patient from UNITED STATES , weighting 368.2 lb, was diagnosed with sedation and was treated with Propofol (View Usage). Patient had the following side effects: blood triglycerides increased. Propofol dosage: 40-80 Mcg/kg/min Iv Drip.

6701525-6 | Hyperthermia Malignant
on Apr 22, 2010 Female patient from UNITED STATES , weighting 38.80 lb, was diagnosed with dental implantation, preoperative care and was treated with Propofol (View Usage). After Propofol was administered, patient had the following side effects: hyperthermia malignant. Propofol dosage: . During the same period patient was treated with ULTANE (View Ultane Review and Ultane Label ), FENTANYL (View Fentanyl Review and Fentanyl Label ), CEFAZOLIN SODIUM (View Cefazolin Sodium Review and Cefazolin Sodium Label ).

6700835-6 | Anaesthetic Complication, Asthenia, Blood Pressure Systolic Increased, Central Nervous System Lesion, Cerebral Haemorrhage, Hypoxia, Respiration Abnormal, Respiratory Acidosis, Respiratory Distress
Patient was taking Propofol (View Usage). Patient experienced the following unwanted or unexpected effects: anaesthetic complication, asthenia, blood pressure systolic increased, central nervous system lesion, cerebral haemorrhage, hypoxia, respiration abnormal, respiratory acidosis, respiratory distress on Apr 14, 2010 from UNITED KINGDOM Additional patient health information: Male patient , child 7 years of age, was diagnosed with induction of anaesthesia and. Propofol dosage: 100 Mg Intravenous (not Otherwise Specified). During the same period patient was treated with ADRENALINE (EPINEPHRINE) (EPINEPHRINE) (View Adrenaline (epinephrine) (epinephrine) Review and Adrenaline (epinephrine) (epinephrine) Label ), ATRACURIUM BESYLATE (View Atracurium Besylate Review and Atracurium Besylate Label ), BUPIVACAIN (BUPIVACAINE HYDROCHLORIDE) (View Bupivacain (bupivacaine Hydrochloride) Review and Bupivacain (bupivacaine Hydrochloride) Label ), DESFLURANE (View Desflurane Review and Desflurane Label ), DEXAMETHASONE (View Dexamethasone Review and Dexamethasone Label ), FENTANYL 100 (View Fentanyl-100 Review and Fentanyl-100 Label ), MORPHINE (View Morphine Review and Morphine Label ).

6698519-6 | Catheterisation Cardiac, Hypotension, Procedural Complication
Adverse event was reported on Apr 26, 2010 by a Male patient taking Propofol (View Usage) (Dosage: 200 Mg X1) was diagnosed with anaesthesia procedure and. Location: UNITED STATES , 52 years of age, Patient had the following side effects: catheterisation cardiac, hypotension, procedural complication. During the same period patient was treated with SUCCINYLCHOLINE (100 Mg X1) (View Succinylcholine Review and Succinylcholine Label ). Patient was hospitalized.

6698106-X | Asthma, Chest Pain, Eye Haemorrhage, Malaise, Multiple Allergies, Oxygen Saturation Decreased, Petechiae, Productive Cough, Respiratory Distress
on Apr 26, 2010 Female patient from UNITED STATES , 60 years of age, weighting 244.0 lb, was diagnosed with anaesthesia procedure and was treated with Propofol (View Usage). After Propofol was administered, patient had the following side effects: asthma (What is asthma?), chest pain (What is chest pain?), eye haemorrhage, malaise, multiple allergies, oxygen saturation decreased, petechiae, productive cough, respiratory distress. Propofol dosage: (35-45 Min? Really Unk).

6692992-5 | Bacteroides Infection, Enterobacter Infection, Haemodialysis, Pleural Effusion, Renal Failure, Respiratory Distress, Septic Shock, Stevens-johnson Syndrome
on Apr 06, 2010 Female patient from NETHERLANDS , 47 years of age, was treated with Propofol (View Usage). Patient experienced the following unwanted or unexpected effects: bacteroides infection, enterobacter infection, haemodialysis, pleural effusion, renal failure, respiratory distress, septic shock, stevens-johnson syndrome. Propofol dosage: Intravenous. During the same period patient was treated with MIDAZOLAM HCL (1 Mg Milligram(s)) (View Midazolam Hcl Review and Midazolam Hcl Label ), LOVENOX (View Lovenox Review and Lovenox Label ), AMOXICILLIN AND CLAVULANATE POTASSIUM (View Amoxicillin And Clavulanate Potassium Review and Amoxicillin And Clavulanate Potassium Label ), (MOPRAL /00661201/) (40 Mg Milligram(s)) (View (mopral /00661201/) Review and (mopral /00661201/) Label ), CANCIDAS (50 Mg Milligram(s)) (View Cancidas Review and Cancidas Label ), NIMBEX (View Nimbex Review and Nimbex Label ), SUFENTA PRESERVATIVE FREE (View Sufenta Preservative Free Review and Sufenta Preservative Free Label ), (VECTARION) (View (vectarion) Review and (vectarion) Label ). Patient was hospitalized.

6682576-7 | Arteriospasm Coronary, Hypotension, Prinzmetal Angina
Patient was taking Propofol (View Usage). Patient had the following side effects: arteriospasm coronary, hypotension, prinzmetal angina on Apr 08, 2010 from TURKEY Additional patient health information: Female patient , 68 years of age, . Propofol dosage: 140 Mg. During the same period patient was treated with FENTANYL (50 Ug) (View Fentanyl Review and Fentanyl Label ), VECURONIUM BROMIDE (7 Mg) (View Vecuronium Bromide Review and Vecuronium Bromide Label ).