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VENLAFAXINE Safety Reports

Total VENLAFAXINE reports: 181.
VENLAFAXINE FDA safety alerts: 2003 2004 2005 2006 .
Reported deaths: 11    Reported hospitalizations: 103.
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Health Professional from GERMANY reported VENLAFAXINE problem on May 14, 2007. Male patient, weighting 5.47 lb, was diagnosed with depression and was treated with VENLAFAXINE. After drug was administered, patient experienced the following problems/side effects: congenital genital malformation. VENLAFAXINE dosage: unknown. Patient recovered.

VENLAFAXINE problem was reported by a Physician from GERMANY on May 29, 2007. Female patient, weighting 196.2 lb, was diagnosed with depression, anxiety and was treated with VENLAFAXINE. After drug was administered, patient experienced the following problems/side effects: paraesthesia, suicidal ideation. VENLAFAXINE dosage: unknown. Patient recovered.

Physician from GERMANY reported VENLAFAXINE problem on May 21, 2007. Female patient, weighting 165.3 lb, was diagnosed with depression, dysthymic disorder and was treated with VENLAFAXINE. After drug was administered, patient experienced the following problems/side effects: blood amylase increased, blood cholesterol increased, hot flush, hyperhidrosis, lipase increased, pancreatitis. VENLAFAXINE dosage: unknown. Patient recovered.

VENLAFAXINE problem was reported by a Health Professional from GERMANY on May 23, 2007. Female patient was diagnosed with anxiety, depression and was treated with VENLAFAXINE. After drug was administered, patient experienced the following problems/side effects: cardiac disorder, intentional overdose, suicide attempt. VENLAFAXINE dosage: 300 MG DAILY. Patient recovered.

Physician from GERMANY reported VENLAFAXINE problem on June 01, 2007. Female patient, weighting 26.46 lb, was treated with VENLAFAXINE. After drug was administered, patient experienced the following problems/side effects: accidental overdose. VENLAFAXINE dosage: 1 TABLET (75 MG). Patient was hospitalized. Patient recovered.

VENLAFAXINE problem was reported by a Consumer or non-health professional from GERMANY on May 30, 2007. Female patient was treated with VENLAFAXINE. After drug was administered, patient experienced the following problems/side effects: anxiety, fatigue, hyperhidrosis, mouth haemorrhage, muscle spasms, muscle twitching, nervousness, nightmare, panic reaction. VENLAFAXINE dosage: 75 MG DAILY. During the same period patient was treated with SALMETIN ROTADISK, SALBUTAMOL. Patient was hospitalized. Patient recovered.

Pharmacist from UNITED STATES reported VENLAFAXINE problem on June 11, 2007. Male patient, 59 years of age, weighting 154.0 lb, was diagnosed with depression and was treated with VENLAFAXINE. After drug was administered, patient experienced the following problems/side effects: abdominal pain, ammonia abnormal, blood creatinine increased, blood culture positive, blood glucose increased, blood magnesium increased, blood potassium decreased, blood pressure systolic increased, blood urea increased. VENLAFAXINE dosage: 75MG DAILY PO. Patient was hospitalized. Patient recovered.

VENLAFAXINE problem was reported by a Health Professional from GERMANY on June 12, 2007. Female patient was diagnosed with depression and was treated with VENLAFAXINE. After drug was administered, patient experienced the following problems/side effects: rectal cancer metastatic. VENLAFAXINE dosage: 150 MG DAILY. Patient recovered.

Physician from GERMANY reported VENLAFAXINE problem on June 13, 2007. Female patient, weighting 5.29 lb, was diagnosed with depression, apathy and was treated with VENLAFAXINE. After drug was administered, patient experienced the following problems/side effects: umbilical cord around neck. VENLAFAXINE dosage: unknown. During the same period patient was treated with FOLIC ACID. Patient recovered.

VENLAFAXINE problem was reported by a Health Professional from GERMANY on June 25, 2007. Female patient, 39 years of age, weighting 165.3 lb, was treated with VENLAFAXINE. After drug was administered, patient experienced the following problems/side effects: coma, intentional overdose, respiratory failure. VENLAFAXINE dosage: unknown. During the same period patient was treated with COCAINE, METHADONE, APONAL. Patient was hospitalized. Patient recovered.

Consumer or non-health professional from UNITED STATES reported VENLAFAXINE problem on June 26, 2007. Male patient, 53 years of age, weighting 160.0 lb, was diagnosed with anxiety, depression and was treated with VENLAFAXINE. After drug was administered, patient experienced the following problems/side effects: abdominal pain upper, anaemia, anxiety, asthenia, asthma, dysphagia, dyspnoea, exercise tolerance decreased, fatigue. VENLAFAXINE dosage: 300MG ONCE DAILY PO. During the same period patient was treated with AMITRIPTYLINE, HYDROCODONE, GABAPENTIN, IBUPROFEN, CYCLOBENZAPRINE. Patient recovered.

VENLAFAXINE problem was reported by a Physician from GERMANY on June 22, 2007. Male patient, 38 years of age, weighting 175.7 lb, was diagnosed with personality disorder and was treated with VENLAFAXINE. After drug was administered, patient experienced the following problems/side effects: restless legs syndrome. VENLAFAXINE dosage: 75 MG PER DAY. During the same period patient was treated with MELPERONE, DIAZEPAM. Patient was hospitalized. Patient recovered.

Pharmacist from UNITED STATES reported VENLAFAXINE problem on June 27, 2007. Male patient, 87 years of age, was diagnosed with depression, neuropathy and was treated with VENLAFAXINE. After drug was administered, patient experienced the following problems/side effects: rash. VENLAFAXINE dosage: 75MG EVERY DAY PO. Patient recovered.

VENLAFAXINE problem was reported by a Consumer or non-health professional from UNITED KINGDOM on June 23, 2006. Female patient, 45 years of age, weighting 231.0 lb, was diagnosed with depression, schizophrenia and was treated with VENLAFAXINE. After drug was administered, patient experienced the following problems/side effects: hepatocellular damage, liver function test abnormal. VENLAFAXINE dosage: 75 MG/DAY. During the same period patient was treated with CLOZARIL. Patient recovered.

Consumer or non-health professional from GERMANY reported VENLAFAXINE problem on June 19, 2006. Female patient, 26 years of age, was diagnosed with anxiety, depression, psychotic disorder and was treated with VENLAFAXINE. After drug was administered, patient experienced the following problems/side effects: condition aggravated, hallucination. VENLAFAXINE dosage: 37.5 MG PER DAY. During the same period patient was treated with SOLIAN, TRUXAL, TEGRETOL. Patient was hospitalized. Patient recovered.

VENLAFAXINE problem was reported by a Consumer or non-health professional from GERMANY on June 28, 2006. Female patient, 75 years of age, was treated with VENLAFAXINE. After drug was administered, patient experienced the following problems/side effects: vith nerve paralysis. VENLAFAXINE dosage: unknown. Patient recovered.

Consumer or non-health professional from GERMANY reported VENLAFAXINE problem on June 27, 2006. Male patient, 14 years of age, was treated with VENLAFAXINE. After drug was administered, patient experienced the following problems/side effects: extrapyramidal disorder, somnolence. VENLAFAXINE dosage: unknown. During the same period patient was treated with METHADONE, MIRTAZAPINE, OPIOIDS, TAXILAN, ZOPICLONE. Patient was hospitalized. Patient recovered.

VENLAFAXINE problem was reported by a Consumer or non-health professional from GERMANY on June 26, 2006. Male patient, 45 years of age, was treated with VENLAFAXINE. After drug was administered, patient experienced the following problems/side effects: anxiety, hallucination, visual, headache, ill-defined disorder, malaise, sinus tachycardia, vertigo. VENLAFAXINE dosage: 75 MG, ORAL. During the same period patient was treated with PROMETHAZINE, MIRTAZAPINE, ZOLOFT, SOLIAN. Patient recovered.

Consumer or non-health professional from GERMANY reported VENLAFAXINE problem on June 26, 2006. Male patient, 50 years of age, was diagnosed with depression and was treated with VENLAFAXINE. After drug was administered, patient experienced the following problems/side effects: abnormal behaviour, delirium, delusion, sleep disorder. VENLAFAXINE dosage: unknown. During the same period patient was treated with LORAZEPAM, MELPERONE. Patient was hospitalized. Patient recovered.

VENLAFAXINE problem was reported by a Consumer or non-health professional from GERMANY on June 26, 2006. Female patient, 67 years of age, was treated with VENLAFAXINE. After drug was administered, patient experienced the following problems/side effects: confusional state, delirium, disorientation, disturbance in attention, memory impairment, restlessness, sleep disorder, speech disorder. VENLAFAXINE dosage: unknown. During the same period patient was treated with AKINETON, ARICEPT, CIPRALEX, HYPNOREX. Patient was hospitalized. Patient recovered.

Health Professional from GERMANY reported VENLAFAXINE problem on June 29, 2006. Female patient, 45 years of age, was treated with VENLAFAXINE. After drug was administered, patient experienced the following problems/side effects: coma, hypotension, respiratory failure, suicide attempt. VENLAFAXINE dosage: 50 CAPSULES (OVERDOSE AMOUNT 3750 MG). During the same period patient was treated with DOXEPIN, KLOSTERFRAU MELISSENGEIST, ZOLPIDEM TARTRATE. Patient was hospitalized. Patient recovered.

VENLAFAXINE problem was reported by a Consumer or non-health professional from GERMANY on June 26, 2006. Male patient, 45 years of age, was treated with VENLAFAXINE. After drug was administered, patient experienced the following problems/side effects: anxiety, hallucination, visual, headache, heart rate increased, malaise, sinus tachycardia, vertigo. VENLAFAXINE dosage: 75 MG ORAL. During the same period patient was treated with PROMETHAZINE, MIRTAZAPINE, ZOLOFT, SOLIAN. Patient recovered.

Consumer or non-health professional from GERMANY reported VENLAFAXINE problem on July 04, 2006. Male patient, 75 years of age, was diagnosed with anxiety, depression and was treated with VENLAFAXINE. After drug was administered, patient experienced the following problems/side effects: vith nerve paralysis. VENLAFAXINE dosage: 75 MG 1X PER 1 DAY ORAL. Patient recovered.

VENLAFAXINE problem was reported by a Consumer or non-health professional from GERMANY on June 29, 2006. Male patient, 21 years of age, was treated with VENLAFAXINE. After drug was administered, patient experienced the following problems/side effects: bradypnoea, miosis, sopor, tachycardia. VENLAFAXINE dosage: unknown. During the same period patient was treated with HEROIN, ROHYPNOL. Patient was hospitalized. Patient recovered.

Health Professional from GERMANY reported VENLAFAXINE problem on July 11, 2006. Male patient, 14 years of age, was treated with VENLAFAXINE. After drug was administered, patient experienced the following problems/side effects: extrapyramidal disorder, overdose, somnolence. VENLAFAXINE dosage: unknown. During the same period patient was treated with METHADONE, MIRTAZAPINE, OPIOIDS, TAXILAN, ZOPICLONE. Patient was hospitalized. Patient recovered.

VENLAFAXINE problem was reported by a Health Professional from GERMANY on July 13, 2006. Male patient, 14 years of age, was treated with VENLAFAXINE. After drug was administered, patient experienced the following problems/side effects: extrapyramidal disorder, intentional overdose, somnolence, suicide attempt. VENLAFAXINE dosage: unknown. During the same period patient was treated with METHADONE, MIRTAZAPINE, OPIOIDS, TAXILAN, ZOPICLONE. Patient was hospitalized. Patient recovered.

Consumer or non-health professional from GERMANY reported VENLAFAXINE problem on July 12, 2006. Male patient was treated with VENLAFAXINE. After drug was administered, patient experienced the following problems/side effects: accidental overdose. VENLAFAXINE dosage: 1 CAPSULE (OVERDOSE AMOUNT 75 MG). Patient was hospitalized. Patient recovered.

VENLAFAXINE problem was reported by a Consumer or non-health professional from UNITED STATES on July 19, 2006. Male patient, weighting 222.4 lb, was diagnosed with depression and was treated with VENLAFAXINE. After drug was administered, patient experienced the following problems/side effects: agitation, dyskinesia, hypertension, mental status changes, paranoia, pyrexia, serotonin syndrome, tachycardia, tachypnoea. VENLAFAXINE dosage: 150MG CAPSULE Q8HOURS PO. Patient recovered.

Consumer or non-health professional from GERMANY reported VENLAFAXINE problem on July 17, 2006. Female patient was diagnosed with anxiety, depression, panic attack and was treated with VENLAFAXINE. After drug was administered, patient experienced the following problems/side effects: idiopathic thrombocytopenic purpura, neonatal disorder. VENLAFAXINE dosage: 75 MG 2X PER 1 DAY. Patient was hospitalized. Patient recovered.

VENLAFAXINE problem was reported by a Consumer or non-health professional from GERMANY on July 18, 2006. Male patient was diagnosed with depression and was treated with VENLAFAXINE. After drug was administered, patient experienced the following problems/side effects: condition aggravated, obesity, spinal disorder. VENLAFAXINE dosage: 150 MG 1X PER 1 DAY ORAL; 150 MG 1X PER 1 DAY; 225 MG, PER DAY ORAL. Patient recovered.

Consumer or non-health professional from GERMANY reported VENLAFAXINE problem on July 17, 2006. Female patient was diagnosed with anxiety, depression, panic attack and was treated with VENLAFAXINE. After drug was administered, patient experienced the following problems/side effects: idiopathic thrombocytopenic purpura, thrombocytopenia neonatal. VENLAFAXINE dosage: 75 MG 2X PER 1 DAY. Patient was hospitalized. Patient recovered.

VENLAFAXINE problem was reported by a Physician from GERMANY on Aug 01, 2006. Female patient, 27 years of age, was diagnosed with post-traumatic stress disorder and was treated with VENLAFAXINE. After drug was administered, patient experienced the following problems/side effects: premature baby, urinary tract infection. VENLAFAXINE dosage: 225 MG PER DAY. During the same period patient was treated with AMOXICILLIN. Patient died.

Health Professional from GERMANY reported VENLAFAXINE problem on July 31, 2006. Female patient, 70 years of age, was treated with VENLAFAXINE. After drug was administered, patient experienced the following problems/side effects: aspiration, atrioventricular block first degree, bradycardia, coma, intentional overdose. VENLAFAXINE dosage: 100 CAPSULES (OVERDOSE MAOUNT 7500MG) ORAL. During the same period patient was treated with MELPERONE, MEMANTINE, REMERON. Patient was hospitalized. Patient recovered.

VENLAFAXINE problem was reported by a Consumer or non-health professional from GERMANY on July 31, 2006. Male patient, 59 years of age, was diagnosed with depression and was treated with VENLAFAXINE. After drug was administered, patient experienced the following problems/side effects: cardiomyopathy, sexual dysfunction, ventricular arrhythmia. VENLAFAXINE dosage: 75 MG 1X PER 1 DAY, ORAL. During the same period patient was treated with MIRTAZAPINE. Patient was hospitalized. Patient recovered.

Consumer or non-health professional from GERMANY reported VENLAFAXINE problem on Aug 01, 2006. Male patient was diagnosed with post-traumatic stress disorder and was treated with VENLAFAXINE. After drug was administered, patient experienced the following problems/side effects: immature respiratory system, iron deficiency anaemia, neonatal disorder, premature baby. VENLAFAXINE dosage: 225 MG PER DAY ORAL. During the same period patient was treated with AMOXICILLIN. Patient was hospitalized. Patient recovered.

VENLAFAXINE problem was reported by a Consumer or non-health professional from GERMANY on Aug 04, 2006. Male patient, 62 years of age, was treated with VENLAFAXINE. After drug was administered, patient experienced the following problems/side effects: cerebrovascular accident. VENLAFAXINE dosage: 75 MG ORAL. Patient died.

Consumer or non-health professional from GERMANY reported VENLAFAXINE problem on Aug 07, 2006. Female patient, 43 years of age, was treated with VENLAFAXINE. After drug was administered, patient experienced the following problems/side effects: depression, nausea, somnolence, stomach discomfort, suicide attempt. VENLAFAXINE dosage: 10 CAPSULES (OVERDOSE AMOUNT 750MG) ORAL. During the same period patient was treated with EDRONAX, IBUPROFEN, LORAZEPAM. Patient was hospitalized. Patient recovered.

VENLAFAXINE problem was reported by a Consumer or non-health professional from GERMANY on Aug 17, 2006. Female patient, 71 years of age, was treated with VENLAFAXINE. After drug was administered, patient experienced the following problems/side effects: aspiration, atrioventricular block first degree, blood creatine phosphokinase increased, bradycardia, coma, suicide attempt, vomiting. VENLAFAXINE dosage: 100 CAPSULES (OVERDOSE MAOUNT 7500MG, ORAL. During the same period patient was treated with MELPERONE, MEMANTINE, REMERON. Patient was hospitalized. Patient recovered.

Consumer or non-health professional from SLOVAKIA (Slovak Republic) reported VENLAFAXINE problem on Aug 22, 2006. Female patient, 35 years of age, was diagnosed with depression and was treated with VENLAFAXINE. After drug was administered, patient experienced the following problems/side effects: intentional overdose, nausea, suicide attempt. VENLAFAXINE dosage: TEN 75 MG CAPSULES (OVERDOSE AMOUNT 750 MG). During the same period patient was treated with ALCOHOL. Patient was hospitalized. Patient recovered.

VENLAFAXINE problem was reported by a Consumer or non-health professional from AUSTRIA on Aug 21, 2006. Female patient, 75 years of age, was diagnosed with depressive symptom and was treated with VENLAFAXINE. After drug was administered, patient experienced the following problems/side effects: blood chloride decreased, blood osmolarity decreased, hyponatraemia, psychotic disorder. VENLAFAXINE dosage: unknown. During the same period patient was treated with ASPIRIN, HYDROCHLOROTHIAZIDE, LISINOPRIL, AMLODIPINE, PRAVASTATIN. Patient was hospitalized. Patient recovered.

Consumer or non-health professional from GERMANY reported VENLAFAXINE problem on Sept 05, 2006. Female patient, 85 years of age, was diagnosed with depression and was treated with VENLAFAXINE. After drug was administered, patient experienced the following problems/side effects: delirium, hallucination, paranoia. VENLAFAXINE dosage: 150 MG DAILY, ORAL. During the same period patient was treated with OXAZEPAM. Patient recovered.

VENLAFAXINE problem was reported by a Consumer or non-health professional from GERMANY on Sept 11, 2006. Female patient, 42 years of age, was treated with VENLAFAXINE. After drug was administered, patient experienced the following problems/side effects: aggression, agitation, alcohol poisoning, intentional overdose, mydriasis, suicide attempt. VENLAFAXINE dosage: 30 CAPSULES (OVERDOSE AMOUNT 2250 MG). During the same period patient was treated with ALCOHOL, VALPROIC ACID. Patient was hospitalized. Patient recovered.

Consumer or non-health professional from JAPAN reported VENLAFAXINE problem on Sept 01, 2006. Female patient, 27 years of age, was diagnosed with tonsillitis, nasopharyngitis and was treated with VENLAFAXINE. After drug was administered, patient experienced the following problems/side effects: acute tonsillitis, pharyngolaryngeal pain. VENLAFAXINE dosage: unknown. During the same period patient was treated with BROACT, ACETAMINOPHEN, CODEINE PHOSPHATE, CLINDAMYCIN HYDROCHLORIDE, MEIACT, MUCOSOLVAN. Patient was hospitalized. Patient recovered.

VENLAFAXINE problem was reported by a Physician from CANADA on Sept 07, 2006. Female patient, 19 years of age, was diagnosed with postpartum depression and was treated with VENLAFAXINE. After drug was administered, patient experienced the following problems/side effects: bipolar ii disorder, brief psychotic disorder, with postpartum onset, insomnia, intentional overdose. VENLAFAXINE dosage: 150 MG, QD. During the same period patient was treated with ACETAMINOPHEN, ZOPICLONE, QUETIAPINE. Patient was hospitalized. Patient recovered.

Consumer or non-health professional from GERMANY reported VENLAFAXINE problem on Sept 07, 2006. Female patient, 37 years of age, was diagnosed with depression and was treated with VENLAFAXINE. After drug was administered, patient experienced the following problems/side effects: caesarean section, haemorrhage, placenta praevia, premature baby, premature separation of placenta. VENLAFAXINE dosage: 300 MG PER DAY. During the same period patient was treated with ENOXAPARIN. Patient was hospitalized. Patient recovered.

VENLAFAXINE problem was reported by a Consumer or non-health professional from SPAIN on Sept 13, 2006. Female patient, 65 years of age, was diagnosed with major depression and was treated with VENLAFAXINE. After drug was administered, patient experienced the following problems/side effects: hyperthermia, neuroleptic malignant syndrome. VENLAFAXINE dosage: 150 MG 1X PER 1 DAY, ORAL. During the same period patient was treated with ANAFRANIL, SEROQUEL. Patient was hospitalized. Patient died.

Consumer or non-health professional from AUSTRIA reported VENLAFAXINE problem on Sept 27, 2006. Male patient, 61 years of age, was diagnosed with bipolar disorder and was treated with VENLAFAXINE. After drug was administered, patient experienced the following problems/side effects: cardiac arrest, vomiting. VENLAFAXINE dosage: 50 MG 1X PER 1 DAY ORAL. During the same period patient was treated with AMLODIPINE, TRAZODONE. Patient died.

VENLAFAXINE problem was reported by a Health Professional from JAPAN on Sept 26, 2006. Female patient, 58 years of age, was diagnosed with depression and was treated with VENLAFAXINE. After drug was administered, patient experienced the following problems/side effects: dizziness, gastrointestinal inflammation, large intestine carcinoma, metastasis, nausea, vomiting. VENLAFAXINE dosage: 75 MG 1X PER 1 DAY. During the same period patient was treated with LENDORM. Patient was hospitalized. Patient recovered.

Consumer or non-health professional from GERMANY reported VENLAFAXINE problem on Sept 22, 2006. Male patient was treated with VENLAFAXINE. After drug was administered, patient experienced the following problems/side effects: hypertonia, nervousness, tremor. VENLAFAXINE dosage: 75MG PER DAY ORAL. Patient recovered.

VENLAFAXINE problem was reported by a Consumer or non-health professional from GERMANY on Sept 22, 2006. Male patient was treated with VENLAFAXINE. After drug was administered, patient experienced the following problems/side effects: hypertonia neonatal, nervousness. VENLAFAXINE dosage: 75 MG PER DAY; TRANSPLACENTAL. Patient recovered.

Health Professional from UNITED STATES reported VENLAFAXINE problem on Oct 17, 2006. Female patient, 86 years of age, was diagnosed with depression and was treated with VENLAFAXINE. After drug was administered, patient experienced the following problems/side effects: asthenia, gait disturbance, lethargy. VENLAFAXINE dosage: 225 MG QD PO. During the same period patient was treated with ADVAIR DISKUS, ARICEPT, ASPIRIN, GLUCOTROL, LASIX, IMDUR, METFORMIN, NAPROSYN. Patient was hospitalized. Patient recovered.

VENLAFAXINE problem was reported by a Physician from UNITED STATES on Oct 31, 2006. Male patient, 42 years of age, weighting 180.0 lb, was diagnosed with depression and was treated with VENLAFAXINE. After drug was administered, patient experienced the following problems/side effects: constipation. VENLAFAXINE dosage: 150 - 300 MG DAILY PO. Patient recovered.

Consumer or non-health professional from GERMANY reported VENLAFAXINE problem on Oct 27, 2006. Female patient, 68 years of age, was treated with VENLAFAXINE. After drug was administered, patient experienced the following problems/side effects: coma, dehydration, hyponatraemia. VENLAFAXINE dosage: 75 MG. During the same period patient was treated with BUPRENORPHINE HYDROCHLORIDE. Patient was hospitalized. Patient recovered.

VENLAFAXINE problem was reported by a Consumer or non-health professional from GERMANY on Oct 25, 2006. Female patient was treated with VENLAFAXINE. After drug was administered, patient experienced the following problems/side effects: coma, dehydration, hyponatraemia. VENLAFAXINE dosage: 75 MG. During the same period patient was treated with BUPRENORPHINE. Patient was hospitalized. Patient recovered.

Consumer or non-health professional from JAPAN reported VENLAFAXINE problem on Oct 21, 2006. Male patient, 27 years of age, was diagnosed with depression and was treated with VENLAFAXINE. After drug was administered, patient experienced the following problems/side effects: cyst, pneumothorax. VENLAFAXINE dosage: unknown. During the same period patient was treated with LENDORM. Patient was hospitalized. Patient recovered.

VENLAFAXINE problem was reported by a Consumer or non-health professional from UNITED STATES on Nov 07, 2006. Female patient, child 11 years of age, weighting 80.00 lb, was diagnosed with anxiety and was treated with VENLAFAXINE. After drug was administered, patient experienced the following problems/side effects: abnormal behaviour, aggression, fatigue, pyrexia, screaming, social avoidant behaviour, suicidal ideation. VENLAFAXINE dosage: 37 MG ONCE DAILY PO. During the same period patient was treated with EFFEXOR. Patient recovered.

Consumer or non-health professional from GERMANY reported VENLAFAXINE problem on Oct 27, 2006. Female patient, 68 years of age, was treated with VENLAFAXINE. After drug was administered, patient experienced the following problems/side effects: coma, dehydration, hyponatraemia. VENLAFAXINE dosage: unknown. During the same period patient was treated with TRANSTEC. Patient was hospitalized. Patient recovered.

VENLAFAXINE problem was reported by a Consumer or non-health professional from GERMANY on Oct 30, 2006. Female patient, 68 years of age, was treated with VENLAFAXINE. After drug was administered, patient experienced the following problems/side effects: coma, dehydration, hyponatraemia. VENLAFAXINE dosage: 75 MG; FOR A LONGER TIME. During the same period patient was treated with BUPRENORPHINE. Patient was hospitalized. Patient recovered.

Consumer or non-health professional from GERMANY reported VENLAFAXINE problem on Nov 08, 2006. Female patient was treated with VENLAFAXINE. After drug was administered, patient experienced the following problems/side effects: angioneurotic oedema. VENLAFAXINE dosage: unknown. During the same period patient was treated with OPIPRAMOL. Patient recovered.

VENLAFAXINE problem was reported by a Consumer or non-health professional from GERMANY on Nov 06, 2006. Female patient, 73 years of age, was diagnosed with depression and was treated with VENLAFAXINE. After drug was administered, patient experienced the following problems/side effects: asthenia, fatigue, hypokalaemia, hyponatraemia. VENLAFAXINE dosage: 75 MG 1X PER 1 DAY ORAL. During the same period patient was treated with METOPROLOL TARTRATE, RAMIPRIL, DELIX PLUS, DISALUNIL, NEXIUM, TOREM, GLUCOBAY. Patient was hospitalized. Patient recovered.

Consumer or non-health professional from GERMANY reported VENLAFAXINE problem on Nov 06, 2006. Female patient, 92 years of age, was treated with VENLAFAXINE. After drug was administered, patient experienced the following problems/side effects: dizziness, hypotonia, supraventricular extrasystoles. VENLAFAXINE dosage: unknown. During the same period patient was treated with METOPROLOL SUCCINATE, PANTOPRAZOLE, SEROQUEL, DIGITOXIN, CYNT, PREDNISOLONE. Patient was hospitalized. Patient recovered.

VENLAFAXINE problem was reported by a Consumer or non-health professional from GERMANY on Nov 06, 2006. Female patient, 68 years of age, was diagnosed with apathy, asthenia, pain and was treated with VENLAFAXINE. After drug was administered, patient experienced the following problems/side effects: apathy, blood alkaline phosphatase increased, blood cholesterol increased, blood creatine phosphokinase increased, blood glucose decreased, blood potassium increased, blood thyroid stimulating hormone increased, blood urea increased, coma. VENLAFAXINE dosage: 75 MG PER DAY. During the same period patient was treated with VENLAFAXINE EXTENDED, VENLAFAXINE EXTENDED, BUPRENORPHINE. Patient was hospitalized. Patient recovered.

Consumer or non-health professional from GERMANY reported VENLAFAXINE problem on Nov 06, 2006. Female patient, 47 years of age, was diagnosed with depression and was treated with VENLAFAXINE. After drug was administered, patient experienced the following problems/side effects: blood pressure increased, blood pressure orthostatic abnormal, dizziness, fall, hyperventilation, sinus tachycardia, syncope. VENLAFAXINE dosage: unknown. Patient was hospitalized. Patient recovered.

VENLAFAXINE problem was reported by a Consumer or non-health professional from GERMANY on Nov 15, 2006. Male patient, 41 years of age, was diagnosed with depression and was treated with VENLAFAXINE. After drug was administered, patient experienced the following problems/side effects: alanine aminotransferase increased, aspartate aminotransferase increased, blood creatine phosphokinase increased, musculoskeletal discomfort. VENLAFAXINE dosage: 225 MG PER DAY ORAL. During the same period patient was treated with MIRTAZAPINE. Patient recovered.

Consumer or non-health professional from AUSTRIA reported VENLAFAXINE problem on Nov 14, 2006. Male patient, 26 years of age, was diagnosed with borderline personality disorder, depression and was treated with VENLAFAXINE. After drug was administered, patient experienced the following problems/side effects: aggression, nightmare, suicidal ideation. VENLAFAXINE dosage: TWICE 150 MG ORAL. During the same period patient was treated with VENLAFAXINE EXTENDED, ANTIPSYCHOTICS. Patient recovered.

VENLAFAXINE problem was reported by a Consumer or non-health professional from GERMANY on Nov 15, 2006. Male patient, 75 years of age, was treated with VENLAFAXINE. After drug was administered, patient experienced the following problems/side effects: alanine aminotransferase increased, aspartate aminotransferase increased, condition aggravated, gamma-glutamyltransferase increased, hepatic enzyme increased, lipase increased. VENLAFAXINE dosage: unknown. During the same period patient was treated with MIRTAZAPINE, RISPERDAL, ASPIRIN. Patient recovered.

Consumer or non-health professional from AUSTRIA reported VENLAFAXINE problem on Nov 17, 2006. Male patient, 26 years of age, was diagnosed with borderline personality disorder, depression and was treated with VENLAFAXINE. After drug was administered, patient experienced the following problems/side effects: aggression, nightmare, suicidal ideation. VENLAFAXINE dosage: TWICE 150 MG. During the same period patient was treated with VENLAFAXINE EXTENDED. Patient recovered.

VENLAFAXINE problem was reported by a Consumer or non-health professional from AUSTRALIA on Nov 17, 2006. Male patient, 26 years of age, was diagnosed with borderline personality disorder, depression and was treated with VENLAFAXINE. After drug was administered, patient experienced the following problems/side effects: aggression, nightmare, suicidal ideation. VENLAFAXINE dosage: TWICE 150 MG; ORAL. During the same period patient was treated with VENLAFAXINE HYDROCHLORIDE. Patient recovered.

Health Professional from UNITED STATES reported VENLAFAXINE problem on Dec 06, 2006. Male patient, 59 years of age, weighting 243.0 lb, was treated with VENLAFAXINE. After drug was administered, patient experienced the following problems/side effects: headache, hypertension. VENLAFAXINE dosage: 150 MG PO BID. Patient was hospitalized. Patient recovered.

VENLAFAXINE problem was reported by a Consumer or non-health professional from GERMANY on Nov 06, 2006. Female patient, 92 years of age, was treated with VENLAFAXINE. After drug was administered, patient experienced the following problems/side effects: dizziness, fall, hypotension, sinus tachycardia, supraventricular extrasystoles. VENLAFAXINE dosage: unknown. During the same period patient was treated with METOPROLOL SUCCINATE, SEROQUEL, DIGITOXIN, CYNT, PREDNISOLONE. Patient was hospitalized. Patient recovered.

Consumer or non-health professional from GERMANY reported VENLAFAXINE problem on Nov 28, 2006. Female patient, 48 years of age, was treated with VENLAFAXINE. After drug was administered, patient experienced the following problems/side effects: bowel sounds abnormal, fatigue, intentional overdose, suicide attempt. VENLAFAXINE dosage: 40 CAPSULES (OVERDOSE AMOUNT 3000 MG). Patient was hospitalized. Patient recovered.

VENLAFAXINE problem was reported by a Consumer or non-health professional from GERMANY on Nov 24, 2006. Female patient, 18 years of age, was treated with VENLAFAXINE. After drug was administered, patient experienced the following problems/side effects: disorientation, dysarthria, intentional overdose, suicide attempt, tachycardia. VENLAFAXINE dosage: unknown. During the same period patient was treated with ABILIFY, VIVINOX SCHLAFDRAGEES. Patient was hospitalized. Patient recovered.

Consumer or non-health professional from GERMANY reported VENLAFAXINE problem on Nov 27, 2006. Male patient, 70 years of age, was treated with VENLAFAXINE. After drug was administered, patient experienced the following problems/side effects: gastrointestinal hypomotility, hypotension, intentional overdose, somnolence, suicide attempt, tachycardia. VENLAFAXINE dosage: 50 CAPSULES (OVERDOSE AMOUNT 3750 MG) ORAL. During the same period patient was treated with SEROQUEL. Patient was hospitalized. Patient recovered.

VENLAFAXINE problem was reported by a Consumer or non-health professional from UNITED STATES on Mar 07, 2006. Female patient, 50 years of age, weighting 138.0 lb, was treated with VENLAFAXINE. After drug was administered, patient experienced the following problems/side effects: diabetes mellitus, pancreatitis. VENLAFAXINE dosage: unknown. During the same period patient was treated with ATENOLOL, ZYPREXA. Patient was hospitalized. Patient died on 10/23/2003.

Consumer or non-health professional from GERMANY reported VENLAFAXINE problem on Dec 08, 2006. Female patient, 58 years of age, was diagnosed with depression and was treated with VENLAFAXINE. After drug was administered, patient experienced the following problems/side effects: hepatic cirrhosis, hepatic steatosis. VENLAFAXINE dosage: 75 MG 1X PER 1 DAY ORAL. Patient recovered.

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Abacavir sulfate
Abatacept
Abilify
Acamprosate calcium
AccuprilThis drug has as active FDA Safety Alert
AccutaneThis drug has as active FDA Safety Alert
AceonThis drug has as active FDA Safety Alert
Aciphex
Actiq (fentanyl citrate)
ActimmuneThis drug has as active FDA Safety Alert
(aripiprazole) (quinapril) (isotretinoin) (perindopril) (rabeprazole) (interferon gamma-1b)
ActonelThis drug has as active FDA Safety Alert (risedronate)
Actoplus MetThis drug has as active FDA Safety Alert (pioglitazone)
ActosThis drug has as active FDA Safety Alert (pioglitazone)
AcuTect (technetium Tc 99m apcitide)
Adefovir dipivoxil
Advair Diskus(Fluticasone propionate; Salmeterol xinafoate)
AdderallThis drug has as active FDA Safety Alert (amphetamine salts)
Agenerase (amprenavir)
Aggrastat (tirofiban)
Alamast (pemirolast)
AlendronateThis drug has as active FDA Safety Alert
AlemtuzumabThis drug has as active FDA Safety Alert
AleveThis drug has as active FDA Safety Alert (naproxen sodium)
Alfuzosin
Alinia (nitazoxanide)
Alimta (pemetrexed)
Alitretinoin
Almotriptan malateThis drug has as active FDA Safety Alert
Alosetron hydrochloride
Aloxi (palonosetron)
Alrex (loteprednol etabonate)
AltaceThis drug has as active FDA Safety Alert (ramipril)
Ambien (zolpidem tartrate)
AmergeThis drug has as active FDA Safety Alert (naratriptan)
Aminolevulinic acid
AmiodaroneThis drug has as active FDA Safety Alert
Amitiza (lubiprostone)
AmnesteemThis drug has as active FDA Safety Alert (isotretinoin)
Amphadase (hyaluronidase)
luronidase)
Amphetamine saltsThis drug has as active FDA Safety Alert
Amprenavir
AnaproxThis drug has as active FDA Safety Alert (naproxen sodium)
Angiomax (bivalirudin)
Anidulafungin
Antagon (ganirelix acetate)
Anthelios SX (avobenzone, ecamsule, octocrylene)
Apidra (insulin glulisine recombinant)
Apokyn (apomorphine)
Aprepitant
Aprotinin
Aptivus (tipranavir)
AranespThis drug has as active FDA Safety Alert (darbepoetin alpha)
Arava (leflunomide)
Arformoterol

Argatroban
ArediaThis drug has as active FDA Safety Alert (pamidronate)
Aripiprazole
Arixtra (fondaparinux)
Aromasin (exemestane)
Arranon (nelarabine)
Arsenic trioxide
Aspirin
Atacand (candesartan cilexetil)
Atazanavir sulfate
AtomoxetineThis drug has as active FDA Safety Alert
Avastin (bevacizumab)
Avelox (moxifloxacin)
Avobenzone, Ecamsule, Octocrylene
Avodart (dutasteride)
Avonex (interferon beta-1a)
AxertThis drug has as active FDA Safety Alert (almotriptan malate)
Azacitidine
Azilect (rasagiline)
Azopt (brinzolamide)

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B
Balsalazide disodium
Baraclude (entecavir)
BenazeprilThis drug has as active FDA Safety Alert
Benicar (olmesartan medoxomil)
Bevacizumab
Bexarotene
BextraThis drug has as active FDA Safety Alert (valdecoxib)
BiaxinThis drug has as active FDA Safety Alert (clarithromycin)
Bimatoprost
Bivalirudin
BonivaThis drug has as active FDA Safety Alert (ibandronate)
Bortezomib
Brinzolamide
Brovana (arformoterol)
BupropionThis drug has as active FDA Safety Alert
Butisol sodium
Byetta (exenatide)


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C
Calfactant
CampathThis drug has as active FDA Safety Alert (alemtuzumab)
Campral (acamprosate calcium)
Cancidas (caspofungin)
Candesartan cilexetil
Capecitabine
CapotenThis drug has as active FDA Safety Alert (captopril)
CaptoprilThis drug has as active FDA Safety Alert
CarbamazepineThis drug has as active FDA Safety Alert
CarbatrolThis drug has as active FDA Safety Alert (carbamazepine)
Carbrital (pentobarbital and carbromal)
Caspofungin
Cefditoren pivoxil
CefepimeThis drug has as active FDA Safety Alert
CeftriaxoneThis drug has as active FDA Safety Alert
CelebrexThis drug has as active FDA Safety Alert (celecoxib)
CelecoxibThis drug has as active FDA Safety Alert
CelexaThis drug has as active FDA Safety Alert (citalopram hydrobromide)
Cetrorelix acetate
Cetrotide (cetrorelix acetate)
Cetuximab
Cevimeline
ChantixThis drug has as active FDA Safety Alert (varenicline)
Cialis (tadalafil)
Cilostazol
Cinacalcet
Cirlesonide
CitalopramThis drug has as active FDA Safety Alert
ClaravisThis drug has as active FDA Safety Alert (isotretinoin)
ClarithromycinThis drug has as active FDA Safety Alert
Clarinex (desloratadine)
Clolar (clofarabine)
Clofarabine
Clozapine
Clozaril (clozapine)
CodeineThis drug has as active FDA Safety Alert
Colazal (balsalazide disodium)
Colesevelam
ColistimethateThis drug has as active FDA Safety Alert
Coly-Mycin M (colistimethate)This drug has as active FDA Safety Alert
Comtan (entacapone)
Concerta (methylphenidate)
Conivaptan
CordaroneThis drug has as active FDA Safety Alert (amiodarone)
CrestorThis drug has as active FDA Safety Alert (rosuvastatin calcium)
Cubicin (daptomycin)
Curosurf (poractant alfa)
CylertThis drug has as active FDA Safety Alert (pemoline)
CymbaltaThis drug has as active FDA Safety Alert (duloxetine)
CytotecThis drug has as active FDA Safety Alert (misoprostol)

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D
Dacogen (decitabine)
Dalfopristin
Dalmane (flurazepam)
Daptomycin
Darbepoetin alphaThis drug has as active FDA Safety Alert
Darifenacin
Darunavir
Dasatinib
Daytrana (methylphenidate transdermal)
DDAVPThis drug has as active FDA Safety Alert (desmopressin)
DDAVP Nasal SprayThis drug has as active FDA Safety Alert (demopressin)
DDAVP Rhinal TubeThis drug has as active FDA Safety Alert (desmopressin)
DDVPThis drug has as active FDA Safety Alert (desmopressin
Decitabine
Deferasirox
Definity (perflutren lipid microspheres)
DepaconThis drug has as active FDA Safety Alert (valproate)
DepakeneThis drug has as active FDA Safety Alert (valproate)
DepakoteThis drug has as active FDA Safety Alert (valproate)
Desloratadine
DesmopressinThis drug has as active FDA Safety Alert
Detrol (tolterodine tartrate)
terodine tartrate)
Dexedrine (dextroamphetamine sulfate)
Dexmedetomidine
Dexmethylphenidate HCl
> Dextroamphetamine sulfate
Diastat AcuDialThis drug has as active FDA Safety Alert
Diazepam rectal gelThis drug has as active FDA Safety Alert
DidronelThis drug has as active FDA Safety Alert (etidronate)
DiprivanThis drug has as active FDA Safety Alert (propofol)
Dofetilide
Doral (quazepam)
Doxercalcif
Drospirenone
DuloxetineThis drug has as active FDA Safety Alert
DuragesicThis drug has as active FDA Safety Alert (fentanyl transdermal system)
Dutasteride

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E

Eculizumab
Edetate disodium
Efalizumab
Efavirenz
EffexorThis drug has as active FDA Safety Alert (venlafaxine)
Elestat (epinastine)
EletriptanThis drug has as active FDA Safety Alert
Elidel (pimecrolimus)
Ellence (epirubicin)
Eloxatin (oxaliplatin)
Emend (aprepitant)
Emtricitabine
Emtriva (emtricitabine)
Enablex (darifenacin)
Enalapril / EnalaprilatThis drug has as active FDA Safety Alert
Endrate (edetate disodium)
Enfuvirtide
Entacapone
Entecavir
Epinastine
Epirubicin
Eplerenone
Epoetin alfaThis drug has as active FDA Safety Alert
EpogenThis drug has as active FDA Safety Alert (epoetin alfa)
Eptifibatide
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Eraxis (anidulafungin)
Erbitux (cetuximab)
Ertaczo (sertaconazole)
EscitalopramThis drug has as active FDA Safety Alert
Estazolam
Eszopiclone
Ethchlorvynol

Ethinyl estradiol
EtidronateThis drug has as active FDA Safety Alert
Evoxac (cevimeline)
Exelon (rivastigmine tartrate)
Exenatide
Exjade (deferasirox)
Exemestane
Extraneal (icodextrin)
Ezetimibe
Ezetimibe/simvastatin

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F
Factive (gemifloxacin mesylate)
Faslodex (fulvestrant)
FelbamateThis drug has as active FDA Safety Alert
FelbatolThis drug has as active FDA Safety Alert (felbamate)
Fentanyl buccal tabletsThis drug has as active FDA Safety Alert
Fentanyl citrate
Fentanyl transdermal systemThis drug has as active FDA Safety Alert
FentoraThis drug has as active FDA Safety Alert (fentanyl buccal tablets)
Ferrlecit (sodium ferric gluconate complex)
Fleet Accu-PrepThis drug has as active FDA Safety Alert (sodium phosphate)
Fleet Phospho-SodaThis drug has as active FDA Safety Alert (sodium phosphate)
FluoxetineThis drug has as active FDA Safety Alert
Flurazepam
Fluticasone propionate
FluvoxamineThis drug has as active FDA Safety Alert
Focalin (dexmethylphenidate)
Focalin XR (dexmethylphenidate)
Fomivirsen
Fondaparinux
Foradil (formoterol fumarate)
Formoterol fumarate
FosamaxThis drug has as active FDA Safety Alert (alendronate)
FosinoprilThis drug has as active FDA Safety Alert
FrovaThis drug has as active FDA Safety Alert (frovatriptan succinate)
Frovatriptan succinateThis drug has as active FDA Safety Alert
Fulvestrant
Fuzeon (enfuvirtide)

G
GabapentinThis drug has as active FDA Safety Alert
GabitrilThis drug has as active FDA Safety Alert (tiagabine)
Gadobenate DimeglumineThis drug has as active FDA Safety Alert
GadodiamideThis drug has as active FDA Safety Alert
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Ganirelix acetate
GatifloxacinThis drug has as active FDA Safety Alert
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Gemifloxacin mesylate
Gemtuzumab ozogamicin
Geodon (ziprasidone)
Gleevec (imatinib mesylate)

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H
Halcion (triazolam)
HaldolThis drug has as active FDA Safety Alert (haloperidol)
Haloperidol
This drug has as active FDA Safety Alert
Hectorol (doxercalcif)
Hepsera (adefovir dipivoxil)
Hyaluronidase
Hydase (hyaluronidase)
Human Secretin

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I
IbandronateThis drug has as active FDA Safety Alert
Ibuprofen
Icodextrin
Iloprost
Imatinib mesylate
Increlex (Mecasermin [rDNA origin]
Infasurf Preservative Free (calfactant)
ImitrexThis drug has as active FDA Safety Alert (sumatriptan)
Innohep (tinzaparin)
Inspra (eplerenone)
Insulin Aspart recombinant
Insulin Detemir recombinant
Insulin Glargine recombinant

Insulin Glulisine recombinant

Intron A (interferon alfa-2b)
Integrilin (eptifibatide)
ifibatide)
Interferon alfa-2b
Interferon beta-1a
Interferon gamma-1bThis drug has as active FDA Safety Alert
Invega (paliperidone)
Iplex  (mecasermin rinfabate)
IressaThis drug has as active FDA Safety Alert (gefitinib)
IsotretinoinThis drug has as active FDA Safety Alert

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J
Januvia (sitagliptin phosphate)

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K
Kaletra (lopinavir; ritonavir)
Kepivance (palifermin)
KeppraThis drug has as active FDA Safety Alert (levetiracetam)
Ketek (telithromycin)
Ketotifen fumarate

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L
LamictalThis drug has as active FDA Safety Alert (lamotrigine)
LamotrigineThis drug has as active FDA Safety Alert
Lantus (insulin glargine recombinant)
Leflunomide
Lenalidomide
Lepirudin recombinant
Levalbuterol
Levemir (insulin detemir recombinant)
LevetiracetamThis drug has as active FDA Safety Alert
Levitra (vardenafil)
Levonorgestrel
Levothyroxine sodium
Levulan Kerastick (aminolevulinic acid)
LexaproThis drug has as active FDA Safety Alert (escitalopram)
Lindane
Linezolid
This drug has as active FDA Safety Alert
LisinoprilThis drug has as active FDA Safety Alert
Lopinavir/ritonavir
Lotemax (loteprednol etabonate)
LotensinThis drug has as active FDA Safety Alert (benazepril)
Loteprednol etabonate
Lotronex (alosetron hydrochloride)
Lubiprostone
Lucentis (ranibizumab)
Lumigan (bimatoprost)
Lunestra (eszopiclone)
LyricaThis drug has as active FDA Safety Alert (pregabalin)

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M
Macugen (pegaptanib)
MagnevistThis drug has as active FDA Safety Alert (gadopentetate dimeglumine)
Maraviroc
MavikThis drug has as active FDA Safety Alert (trandolapril)
MaxaltThis drug has as active FDA Safety Alert (rizatriptan benzoate)
MaxipimeThis drug has as active FDA Safety Alert (cefepime)
Mecasermin [rDNA origin]
Mecasermin-rinfabate
Meloxicam
Memantine
Metadate CD (methylphenidate HCl)
ylphenidate HCl)
Methylphenidate HCl
Methylphenidate transdermal
Mequinol
Micafungin
Micardis (telmisartan)
misartan)
MifeprexThis drug has as active FDA Safety Alert (mifepristone)
MifepristoneThis drug has as active FDA Safety Alert
Miglustat
MinirinThis drug has as active FDA Safety Alert (desmopressin)
MirtazapineThis drug has as active FDA Safety Alert
MisoprostolThis drug has as active FDA Safety Alert
Mobic (meloxicam)
Modafinil
MoexiprilThis drug has as active FDA Safety Alert
MonoprilThis drug has as active FDA Safety Alert (fosinopril)
Moxifloxacin
MultiHanceThis drug has as active FDA Safety Alert (gadobenate dimeglumine)
Mycamine (micafungin)
Mylotarg (gemtuzumab ozogamicin)

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N
Namenda (memantine)
NaprosynThis drug has as active FDA Safety Alert (naproxen)
NaproxenThis drug has as active FDA Safety Alert
Naratriptan
Nesiritide recombinant
Nateglinide
Natrecor (nesiritide recombinant)
NefazodoneThis drug has as active FDA Safety Alert
Nelarabine
NeoTect Kit (technetium Tc 99m depreotide)
Nesiritide recombinant
NeurontinThis drug has as active FDA Safety Alert (gabapentin)
Nexavar (sorafenib)
Nitazoxanide
Nitisinone
Norelgestromin
NovoLog (insulin aspart recombinant)
Noxafil (posaconazole)

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O
Olanzapine
Olanzapine/fluoxetineThis drug has as active FDA Safety Alert
Olmesartan medoxomil
Omacor (omega-3-acid ethyl esters)
OmalizumabThis drug has as active FDA Safety Alert
Omega-3-acid ethyl esters
Omnaris (cirlesonide)
OmniscanThis drug has as active FDA Safety Alert (gadodiamide)
OptiMARK (gadoversetamide)
Optison (perflutren protein-type A microspheres)
Orencia (abatacept)
Orfadin (nitisinone)
Orlistat
Ortho Evra (norelgestromin; ethinyl estradiol)
Oseltamivir phosphate
OsmoprepThis drug has as active FDA Safety Alert (sodium phosphate)
Oxaliplatin
OxcarbazepineThis drug has as active FDA Safety Alert


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P
PaceroneThis drug has as active FDA Safety Alert (amiodarone)
Palifermin
Paliperidone
Pamidronate