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STRATTERA Safety Reports

Total STRATTERA reports: 657.
STRATTERA FDA safety alerts: 2004 2005 .
Reported deaths: 39    Reported hospitalizations: 181.
Take STRATTERA Side Effects Survey or Share Your STRATTERA Story. STRATTERA Usage.

Showing 1-75 of 657 Next >

Physician from UNITED STATES reported STRATTERA problem on Feb 07, 2007. Male patient, 14 years of age, weighting 119.5 lb, was diagnosed with attention deficit/hyperactivity disorder and was treated with STRATTERA. After drug was administered, patient experienced the following problems/side effects: chest pain, dizziness, loss of consciousness, tachycardia. STRATTERA dosage: 60 MG, UNK. During the same period patient was treated with WELLBUTRIN. Patient recovered.

STRATTERA problem was reported by a Physician from PUERTO RICO on Jan 30, 2007. Male patient, child 9 years of age, weighting 74.99 lb, was diagnosed with attention deficit/hyperactivity disorder and was treated with STRATTERA. After drug was administered, patient experienced the following problems/side effects: completed suicide. STRATTERA dosage: 18 MG, UNK. Patient died on 12/01/2005.

Pharmacist from UNITED STATES reported STRATTERA problem on Feb 16, 2007. Female patient, 14 years of age, weighting 117.9 lb, was diagnosed with attention deficit/hyperactivity disorder and was treated with STRATTERA. After drug was administered, patient experienced the following problems/side effects: abnormal behaviour, depressed level of consciousness, family stress, incorrect dose administered, sleep disorder, suicide attempt. STRATTERA dosage: 80MG DAILY PO. During the same period patient was treated with SEASONALE. Patient was hospitalized. Patient recovered.

STRATTERA problem was reported by a Physician from UNITED STATES on Feb 09, 2007. Male patient, 15 years of age, was diagnosed with attention deficit/hyperactivity disorder and was treated with STRATTERA. After drug was administered, patient experienced the following problems/side effects: optic nerve disorder, optic neuritis, sinusitis, skin papilloma. STRATTERA dosage: 80 MG, DAILY (1/D). Patient recovered.

Physician from CANADA reported STRATTERA problem on Feb 09, 2007. Male patient, 17 years of age, weighting 141.1 lb, was diagnosed with attention deficit/hyperactivity disorder and was treated with STRATTERA. After drug was administered, patient experienced the following problems/side effects: alanine aminotransferase increased, blood creatine phosphokinase increased, fatigue, high density lipoprotein decreased, malaise. STRATTERA dosage: 40 MG, DAILY (1/D). During the same period patient was treated with ACCUTANE. Patient recovered.

STRATTERA problem was reported by a Physician from GERMANY on Feb 08, 2007. Male patient, 25 years of age, weighting 165.3 lb, was diagnosed with attention deficit/hyperactivity disorder and was treated with STRATTERA. After drug was administered, patient experienced the following problems/side effects: intentional overdose, suicide attempt. STRATTERA dosage: 960 MG, UNK. During the same period patient was treated with PIPAMPERONE. Patient was hospitalized. Patient recovered.

Physician from GERMANY reported STRATTERA problem on Feb 08, 2007. Female patient, 17 years of age, was diagnosed with attention deficit/hyperactivity disorder and was treated with STRATTERA. After drug was administered, patient experienced the following problems/side effects: amenorrhoea. STRATTERA dosage: 60 MG, DAILY (1/D). Patient recovered.

STRATTERA problem was reported by a Physician from BELGIUM on Feb 09, 2007. Male patient, 16 years of age, was diagnosed with attention deficit/hyperactivity disorder and was treated with STRATTERA. After drug was administered, patient experienced the following problems/side effects: convulsion, syncope. STRATTERA dosage: unknown. Patient recovered.

Physician from UNITED KINGDOM reported STRATTERA problem on Feb 08, 2007. Male patient, child 12 years of age, was diagnosed with attention deficit/hyperactivity disorder and was treated with STRATTERA. After drug was administered, patient experienced the following problems/side effects: blood alkaline phosphatase increased, jaundice. STRATTERA dosage: unknown. Patient recovered.

STRATTERA problem was reported by a Pharmacist from UNITED STATES on Feb 20, 2007. Male patient, weighting 80.25 lb, was diagnosed with attention deficit/hyperactivity disorder and was treated with STRATTERA. After drug was administered, patient experienced the following problems/side effects: suicidal ideation, suicide attempt. STRATTERA dosage: 25 MG ONCE DAILY PO. Patient was hospitalized. Patient recovered.

Physician from GERMANY reported STRATTERA problem on Feb 14, 2007. Male patient, 14 years of age, was diagnosed with attention deficit/hyperactivity disorder and was treated with STRATTERA. After drug was administered, patient experienced the following problems/side effects: pancreatitis. STRATTERA dosage: unknown. Patient was hospitalized. Patient recovered.

STRATTERA problem was reported by a Health Professional from UNITED STATES on Feb 26, 2007. Male patient, weighting 50.00 lb, was diagnosed with attention deficit/hyperactivity disorder and was treated with STRATTERA. After drug was administered, patient experienced the following problems/side effects: agitation, dysuria, feelings of worthlessness, hallucination, auditory. STRATTERA dosage: 18 MG TWICE DAILY PO. Patient recovered.

Physician from GERMANY reported STRATTERA problem on Feb 15, 2007. Male patient, 14 years of age, was diagnosed with attention deficit/hyperactivity disorder and was treated with STRATTERA. After drug was administered, patient experienced the following problems/side effects: collapse of lung. STRATTERA dosage: 18 MG, DAILY (1/D). Patient was hospitalized. Patient recovered.

STRATTERA problem was reported by a Physician from GERMANY on Feb 15, 2007. Male patient, 15 years of age, weighting 164.0 lb, was diagnosed with attention deficit/hyperactivity disorder and was treated with STRATTERA. After drug was administered, patient experienced the following problems/side effects: angiopathy, fall, myelitis, paresis, urinary retention. STRATTERA dosage: 60 MG, DAILY (1/D). Patient was hospitalized and became disabled. Patient recovered.

Physician from CHILE reported STRATTERA problem on Feb 15, 2007. Male patient, 17 years of age, was diagnosed with attention deficit/hyperactivity disorder, personality disorder and was treated with STRATTERA. After drug was administered, patient experienced the following problems/side effects: extrapyramidal disorder, intentional overdose, suicide attempt. STRATTERA dosage: 800 MG, DAILY (1/D). During the same period patient was treated with VALPROIC ACID, VALPROIC ACID, SPIRON, SOCIAN, RAVOTRIL, PAROXETINE. Patient was hospitalized. Patient recovered.

STRATTERA problem was reported by a Consumer or non-health professional from UNITED STATES on Mar 22, 2006. Male patient, 14 years of age, weighting 349.9 lb, was diagnosed with attention deficit/hyperactivity disorder and was treated with STRATTERA. After drug was administered, patient experienced the following problems/side effects: weight decreased, weight increased. STRATTERA dosage: 80 MG. During the same period patient was treated with PROZAC, CLONIDINE. Patient recovered.

Consumer or non-health professional from UNITED STATES reported STRATTERA problem on Aug 15, 2006. Female patient, 53 years of age, was diagnosed with attention deficit/hyperactivity disorder, depression and was treated with STRATTERA. After drug was administered, patient experienced the following problems/side effects: accidental overdose, dyslexia, feeling abnormal, nerve injury, panic attack, psychomotor hyperactivity. STRATTERA dosage: 80 MG. During the same period patient was treated with PROZAC, OXYCODONE, KLONOPIN, TRIAMTERENE, ALBUTEROL, AZAMACORT, POTASSIUM, FIORINAL. Patient recovered.

STRATTERA problem was reported by a Consumer or non-health professional from UNITED STATES on Nov 09, 2006. Female patient, 55 years of age, was diagnosed with depression and was treated with STRATTERA. After drug was administered, patient experienced the following problems/side effects: disturbance in attention, endometrial hyperplasia, hypertension, nausea, overweight, psychiatric symptom, tinnitus. STRATTERA dosage: 50 MG. During the same period patient was treated with CYMBALTA, PROVIGIL, KLONOPIN, FLUOXETINE. Patient recovered.

Physician from CANADA reported STRATTERA problem on Feb 16, 2007. Female patient, child 8 years of age, was treated with STRATTERA. After drug was administered, patient experienced the following problems/side effects: tuberculosis. STRATTERA dosage: unknown. Patient recovered.

STRATTERA problem was reported by a Physician from BELGIUM on Feb 21, 2007. Female patient, child 7 years of age, weighting 54.90 lb, was diagnosed with attention deficit/hyperactivity disorder and was treated with STRATTERA. After drug was administered, patient experienced the following problems/side effects: abnormal behaviour, affect lability, aggression, agitation, depressed mood, enuresis, negativism, suicidal ideation. STRATTERA dosage: 29 MG, DAILY (1/D). During the same period patient was treated with RILATINE. Patient recovered.

Physician from AUSTRIA reported STRATTERA problem on Feb 21, 2007. Female patient, 16 years of age, weighting 161.6 lb, was diagnosed with attention deficit/hyperactivity disorder, aggression and was treated with STRATTERA. After drug was administered, patient experienced the following problems/side effects: impulse-control disorder, restlessness, sleep disorder. STRATTERA dosage: 72 MG, DAILY (1/D). During the same period patient was treated with TRUXAL. Patient was hospitalized. Patient recovered.

STRATTERA problem was reported by a Physician from CANADA on Feb 20, 2007. Male patient was diagnosed with attention deficit/hyperactivity disorder and was treated with STRATTERA. After drug was administered, patient experienced the following problems/side effects: conduct disorder, fatigue. STRATTERA dosage: 60 MG, UNK. Patient recovered.

Physician from UNITED STATES reported STRATTERA problem on Feb 20, 2007. Male patient, 15 years of age, was diagnosed with attention deficit/hyperactivity disorder and was treated with STRATTERA. After drug was administered, patient experienced the following problems/side effects: suicide attempt. STRATTERA dosage: 80 MG, UNK. Patient was hospitalized. Patient recovered.

STRATTERA problem was reported by a Consumer or non-health professional from UNITED STATES on Feb 22, 2007. Female patient, child 8 years of age, weighting 53.35 lb, was diagnosed with pain, enterobiasis and was treated with STRATTERA. After drug was administered, patient experienced the following problems/side effects: cholestasis, chromaturia, enterobiasis, hepatitis, hypertension, nausea, prothrombin time prolonged, pruritus, rash. STRATTERA dosage: 25 MG, UNK. During the same period patient was treated with MEBENDAZOLE. Patient was hospitalized. Patient recovered.

Physician from UNITED STATES reported STRATTERA problem on Feb 22, 2007. Male patient, 14 years of age, weighting 138.9 lb, was diagnosed with attention deficit/hyperactivity disorder and was treated with STRATTERA. After drug was administered, patient experienced the following problems/side effects: abdominal pain, bone marrow failure, fatigue, hepatitis, neutropenia, thrombocytopenia. STRATTERA dosage: 80 MG, DAILY (1/D). During the same period patient was treated with ZOLOFT. Patient was hospitalized. Patient recovered.

STRATTERA problem was reported by a Physician from UNITED STATES on Feb 22, 2007. Female patient, 31 years of age, weighting 146.3 lb, was treated with STRATTERA. After drug was administered, patient experienced the following problems/side effects: autoimmune hepatitis, hepatitis cholestatic, hepatitis viral, jaundice, liver disorder, nausea. STRATTERA dosage: 40 MG, DAILY (1/D). During the same period patient was treated with WELLBUTRIN. Patient recovered.

Consumer or non-health professional from UNITED STATES reported STRATTERA problem on Mar 07, 2007. Male patient, 25 years of age, weighting 155.0 lb, was diagnosed with attention deficit/hyperactivity disorder and was treated with STRATTERA. After drug was administered, patient experienced the following problems/side effects: visual acuity reduced. STRATTERA dosage: unknown. Patient recovered.

STRATTERA problem was reported by a Physician from AUSTRALIA on Feb 23, 2007. Male patient, child 7 years of age, weighting 57.32 lb, was diagnosed with attention deficit/hyperactivity disorder and was treated with STRATTERA. After drug was administered, patient experienced the following problems/side effects: supraventricular tachycardia. STRATTERA dosage: 10 MG, DAILY (1/D). Patient recovered.

Physician from UNITED STATES reported STRATTERA problem on Feb 26, 2007. Male patient, child 5 years of age, was treated with STRATTERA. After drug was administered, patient experienced the following problems/side effects: hydronephrosis. STRATTERA dosage: unknown. During the same period patient was treated with RISPERDAL. Patient was hospitalized. Patient recovered.

STRATTERA problem was reported by a Physician from UNITED STATES on Feb 26, 2007. Male patient, 21 years of age, was treated with STRATTERA. After drug was administered, patient experienced the following problems/side effects: convulsion, loss of consciousness. STRATTERA dosage: unknown. During the same period patient was treated with AMNESTEEM. Patient recovered.

Consumer or non-health professional from UNITED STATES reported STRATTERA problem on Feb 26, 2007. Male patient, child 7 years of age, was diagnosed with attention deficit/hyperactivity disorder and was treated with STRATTERA. After drug was administered, patient experienced the following problems/side effects: dehydration, dysarthria, fatigue, headache, heart rate increased, lethargy, neck pain, oral discharge. STRATTERA dosage: 18 MG, DAILY (1/D). During the same period patient was treated with ACETAMINOPHEN. Patient was hospitalized. Patient recovered.

STRATTERA problem was reported by a Physician from GERMANY on Feb 26, 2007. Male patient, 28 years of age, weighting 191.8 lb, was diagnosed with attention deficit/hyperactivity disorder, diabetes mellitus insulin-dependent and was treated with STRATTERA. After drug was administered, patient experienced the following problems/side effects: hypoglycaemia. STRATTERA dosage: 60 MG, DAILY (1/D). During the same period patient was treated with HUMALOG, EFEROX. Patient recovered.

Physician from UNITED KINGDOM reported STRATTERA problem on Feb 27, 2007. Male patient, child 5 years of age, weighting 50.16 lb, was diagnosed with attention deficit/hyperactivity disorder, ear infection, chest discomfort and was treated with STRATTERA. After drug was administered, patient experienced the following problems/side effects: abnormal behaviour, anxiety, blood pressure increased, fear, hallucination. STRATTERA dosage: 10 MG, UNK. During the same period patient was treated with AMOXICILLIN, BECOTIDE, FISH OIL, VENTOLIN. Patient recovered.

STRATTERA problem was reported by a Physician from UNITED STATES on Feb 28, 2007. Male patient, 15 years of age, was treated with STRATTERA. After drug was administered, patient experienced the following problems/side effects: jaundice, liver function test abnormal. STRATTERA dosage: unknown. Patient recovered.

Physician from UNITED STATES reported STRATTERA problem on Feb 28, 2007. Male patient, 19 years of age, weighting 154.3 lb, was diagnosed with attention deficit/hyperactivity disorder, sedation and was treated with STRATTERA. After drug was administered, patient experienced the following problems/side effects: abnormal behaviour, aggression, agitation, cardiac murmur, depressed level of consciousness, electrocardiogram qt prolonged, hallucination, auditory, hallucination, visual, intentional overdose. STRATTERA dosage: 1200 MG, OTHER. During the same period patient was treated with OLANZAPINE, OXCARBAZEPINE, QUETIAPINE FUMARATE, PAROXETINE, ALBUTEROL, MONTELUKAST, ATIVAN. Patient was hospitalized. Patient recovered.

STRATTERA problem was reported by a Physician from CANADA on Mar 01, 2007. Male patient was diagnosed with attention deficit/hyperactivity disorder and was treated with STRATTERA. After drug was administered, patient experienced the following problems/side effects: educational problem, fatigue, impulsive behaviour. STRATTERA dosage: 60 MG, UNK. Patient recovered.

Physician from UNITED KINGDOM reported STRATTERA problem on Mar 02, 2007. Male patient, child 10 years of age, weighting 68.34 lb, was diagnosed with attention deficit/hyperactivity disorder and was treated with STRATTERA. After drug was administered, patient experienced the following problems/side effects: confusional state, cyanosis, depression, feeling abnormal, feeling cold, loss of consciousness, malaise, nasopharyngitis, pallor. STRATTERA dosage: 40 MG, DAILY (1/D). Patient recovered.

STRATTERA problem was reported by a Physician from UNITED KINGDOM on Mar 05, 2007. Female patient, 15 years of age, weighting 83.99 lb, was diagnosed with attention deficit/hyperactivity disorder and was treated with STRATTERA. After drug was administered, patient experienced the following problems/side effects: intentional overdose, mydriasis, tachycardia. STRATTERA dosage: 50 MG, DAILY (1/D). During the same period patient was treated with RITALIN. Patient was hospitalized. Patient recovered.

Physician from UNITED STATES reported STRATTERA problem on Mar 05, 2007. Male patient, 16 years of age, was treated with STRATTERA. After drug was administered, patient experienced the following problems/side effects: skin discolouration. STRATTERA dosage: 80 MG, DAILY (1/D). Patient recovered.

STRATTERA problem was reported by a Physician from UNITED STATES on Mar 05, 2007. Female patient, 14 years of age, was treated with STRATTERA. After drug was administered, patient experienced the following problems/side effects: hypoaesthesia, skin discolouration. STRATTERA dosage: 80 MG, DAILY (1/D). Patient recovered.

Physician from UNITED STATES reported STRATTERA problem on Mar 05, 2007. Male patient, 15 years of age, was treated with STRATTERA. After drug was administered, patient experienced the following problems/side effects: peripheral coldness, skin discolouration. STRATTERA dosage: 80 MG, DAILY (1/D). Patient recovered.

STRATTERA problem was reported by a Physician from CANADA on Mar 07, 2007. Male patient, 17 years of age, weighting 141.1 lb, was diagnosed with attention deficit/hyperactivity disorder and was treated with STRATTERA. After drug was administered, patient experienced the following problems/side effects: alanine aminotransferase increased, blood creatine phosphokinase increased, fatigue, high density lipoprotein decreased, malaise. STRATTERA dosage: 40 MG, DAILY (1/D). Patient recovered.

Physician from GERMANY reported STRATTERA problem on Mar 06, 2007. Male patient, 28 years of age, weighting 191.8 lb, was diagnosed with attention deficit/hyperactivity disorder, diabetes mellitus insulin-dependent and was treated with STRATTERA. After drug was administered, patient experienced the following problems/side effects: hypoglycaemia, vomiting. STRATTERA dosage: 40 MG, DAILY (1/D). During the same period patient was treated with HUMALOG, EFEROX. Patient recovered.

STRATTERA problem was reported by a Consumer or non-health professional from UNITED STATES on Mar 07, 2007. Male patient, 19 years of age, was diagnosed with attention deficit/hyperactivity disorder and was treated with STRATTERA. After drug was administered, patient experienced the following problems/side effects: abdominal discomfort, blood lactate dehydrogenase increased, cough, sputum abnormal. STRATTERA dosage: 80 MG, UNK. Patient recovered.

Physician from PUERTO RICO reported STRATTERA problem on Mar 09, 2007. Male patient, child 9 years of age, weighting 74.99 lb, was diagnosed with attention deficit/hyperactivity disorder and was treated with STRATTERA. After drug was administered, patient experienced the following problems/side effects: completed suicide, injury asphyxiation. STRATTERA dosage: 18 MG, UNK. Patient died on 12/05/2005.

STRATTERA problem was reported by a Physician from UNITED STATES on Mar 07, 2007. Female patient was diagnosed with attention deficit/hyperactivity disorder and was treated with STRATTERA. After drug was administered, patient experienced the following problems/side effects: ileus, oedema. STRATTERA dosage: 100 MG, UNK. During the same period patient was treated with LEXAPRO, NEXIUM, CLARINEX, HYDROCHLOROTHIAZIDE. Patient was hospitalized. Patient recovered.

Consumer or non-health professional from UNITED STATES reported STRATTERA problem on Mar 20, 2007. Male patient, child 8 years of age, weighting 50.00 lb, was diagnosed with attention deficit/hyperactivity disorder and was treated with STRATTERA. After drug was administered, patient experienced the following problems/side effects: heart rate increased. STRATTERA dosage: 18MG 1 DAILY FOR 4 DAYS PO. Patient recovered.

STRATTERA problem was reported by a Physician from GERMANY on Mar 12, 2007. Male patient, child 12 years of age, weighting 114.4 lb, was diagnosed with attention deficit/hyperactivity disorder and was treated with STRATTERA. After drug was administered, patient experienced the following problems/side effects: depression, intentional self-injury, suicidal ideation. STRATTERA dosage: 25 MG, EACH MORNING. Patient recovered.

Physician from UNITED STATES reported STRATTERA problem on Mar 12, 2007. Male patient, child 10 years of age, was treated with STRATTERA. After drug was administered, patient experienced the following problems/side effects: chest pain, supraventricular tachycardia. STRATTERA dosage: 36 MG, DAILY (1/D). Patient recovered.

STRATTERA problem was reported by a Physician from UNITED KINGDOM on Mar 12, 2007. Male patient, 13 years of age, weighting 123.5 lb, was diagnosed with attention deficit/hyperactivity disorder, epilepsy and was treated with STRATTERA. After drug was administered, patient experienced the following problems/side effects: anaphylactoid reaction, confusional state, dizziness, feeling cold, hyperhidrosis, loss of consciousness, rash erythematous, somnolence, vertigo. STRATTERA dosage: 25 MG, UNK. During the same period patient was treated with TEGRETOL, RITALIN, CONCERTA. Patient recovered.

Physician from AUSTRIA reported STRATTERA problem on Mar 14, 2007. Female patient, 16 years of age, weighting 161.6 lb, was diagnosed with attention deficit/hyperactivity disorder, aggression and was treated with STRATTERA. After drug was administered, patient experienced the following problems/side effects: impulse-control disorder, restlessness, sleep disorder. STRATTERA dosage: 72 MG, DAILY (1/D). During the same period patient was treated with TRUXAL. Patient was hospitalized. Patient recovered.

STRATTERA problem was reported by a Pharmacist from UNITED STATES on Mar 27, 2007. Male patient, child 7 years of age, weighting 48.50 lb, was diagnosed with attention deficit/hyperactivity disorder and was treated with STRATTERA. After drug was administered, patient experienced the following problems/side effects: aggression, mania. STRATTERA dosage: 60 MG DAILY PO. Patient was hospitalized and became disabled. Patient recovered.

Physician from UNITED STATES reported STRATTERA problem on Mar 14, 2007. Male patient, child 10 years of age, was treated with STRATTERA. After drug was administered, patient experienced the following problems/side effects: accident, dysphagia, trismus. STRATTERA dosage: unknown. During the same period patient was treated with ZOLOFT, RISPERDAL. Patient recovered.

STRATTERA problem was reported by a Physician from UNITED KINGDOM on Mar 14, 2007. Male patient, 15 years of age, was diagnosed with attention deficit/hyperactivity disorder and was treated with STRATTERA. After drug was administered, patient experienced the following problems/side effects: depression, psychomotor retardation, social avoidant behaviour, tearfulness. STRATTERA dosage: 70 MG, UNK. During the same period patient was treated with CANNABIS. Patient recovered.

Physician from CANADA reported STRATTERA problem on Mar 14, 2007. Male patient, child 9 years of age, was treated with STRATTERA. After drug was administered, patient experienced the following problems/side effects: electrocardiogram qt prolonged. STRATTERA dosage: unknown. Patient recovered.

STRATTERA problem was reported by a Consumer or non-health professional from UNITED STATES on Mar 15, 2007. Male patient, 13 years of age, was diagnosed with attention deficit/hyperactivity disorder, blood growth hormone and was treated with STRATTERA. After drug was administered, patient experienced the following problems/side effects: conduct disorder, convulsion, gaze palsy, tremor, unresponsive to stimuli. STRATTERA dosage: 25 MG, DAILY (1/D). During the same period patient was treated with HUMATROPE. Patient recovered.

Physician from UNITED STATES reported STRATTERA problem on Mar 16, 2007. Male patient, child 7 years of age, was diagnosed with attention deficit/hyperactivity disorder, sleep disorder and was treated with STRATTERA. After drug was administered, patient experienced the following problems/side effects: aggression, convulsion, pyromania, snoring, somnolence. STRATTERA dosage: 2 MG/KG, UNK. During the same period patient was treated with ZOLOFT, RISPERDAL, MELATONIN. Patient was hospitalized. Patient recovered.

STRATTERA problem was reported by a Physician from UNITED STATES on Mar 16, 2007. Male patient, 14 years of age, weighting 119.5 lb, was diagnosed with attention deficit/hyperactivity disorder and was treated with STRATTERA. After drug was administered, patient experienced the following problems/side effects: chest pain, dizziness, dyspnoea, electrocardiogram abnormal, epistaxis, loss of consciousness, panic attack, rhinitis allergic, scleritis. STRATTERA dosage: 60 MG, UNK. During the same period patient was treated with WELLBUTRIN. Patient recovered.

Health Professional from UNITED STATES reported STRATTERA problem on Mar 29, 2007. Male patient, 44 years of age, weighting 195.0 lb, was diagnosed with attention deficit/hyperactivity disorder and was treated with STRATTERA. After drug was administered, patient experienced the following problems/side effects: abnormal behaviour, aggression, agitation, amnesia, insomnia, poor quality sleep, psychotic disorder. STRATTERA dosage: unknown. Patient recovered.

STRATTERA problem was reported by a Physician from UNITED STATES on Mar 19, 2007. Male patient, 21 years of age, was treated with STRATTERA. After drug was administered, patient experienced the following problems/side effects: convulsion, loss of consciousness. STRATTERA dosage: unknown. During the same period patient was treated with AMNESTEEM. Patient recovered.

Physician from UNITED STATES reported STRATTERA problem on Mar 19, 2007. Male patient, 15 years of age, was diagnosed with attention deficit/hyperactivity disorder and was treated with STRATTERA. After drug was administered, patient experienced the following problems/side effects: abdominal pain, chromaturia, fatigue, jaundice, liver function test abnormal, prescribed overdose. STRATTERA dosage: 60 MG, EACH MORNING. Patient recovered.

STRATTERA problem was reported by a Physician from UNITED STATES on Mar 20, 2007. Female patient, 25 years of age, was treated with STRATTERA. After drug was administered, patient experienced the following problems/side effects: dizziness postural, syncope. STRATTERA dosage: unknown. Patient recovered.

Physician from AUSTRIA reported STRATTERA problem on Mar 20, 2007. Male patient, child 9 years of age, was diagnosed with attention deficit/hyperactivity disorder and was treated with STRATTERA. After drug was administered, patient experienced the following problems/side effects: decreased appetite, rash. STRATTERA dosage: 18 MG, DAILY (1/D). Patient recovered.

STRATTERA problem was reported by a Consumer or non-health professional from UNITED STATES on Mar 21, 2007. Male patient, child 10 years of age, weighting 125.0 lb, was diagnosed with attention deficit/hyperactivity disorder, anxiety and was treated with STRATTERA. After drug was administered, patient experienced the following problems/side effects: feeling abnormal, head injury, loss of consciousness, post concussion syndrome. STRATTERA dosage: 40 MG, UNK. During the same period patient was treated with KLONOPIN. Patient recovered.

Physician from IRELAND reported STRATTERA problem on Mar 20, 2007. Male patient, 14 years of age, was diagnosed with attention deficit/hyperactivity disorder and was treated with STRATTERA. After drug was administered, patient experienced the following problems/side effects: abdominal pain, gastric ulcer. STRATTERA dosage: 25 MG, UNK. Patient recovered.

STRATTERA problem was reported by a Physician from UNITED STATES on Mar 20, 2007. Male patient, 22 years of age, was diagnosed with attention deficit/hyperactivity disorder and was treated with STRATTERA. After drug was administered, patient experienced the following problems/side effects: haematemesis. STRATTERA dosage: 40 MG, UNK. During the same period patient was treated with NARCAN, NEURONTIN, RITALIN, ULTRAM. Patient recovered.

Physician from GERMANY reported STRATTERA problem on Mar 21, 2007. Male patient, 15 years of age, was diagnosed with attention deficit/hyperactivity disorder and was treated with STRATTERA. After drug was administered, patient experienced the following problems/side effects: migraine with aura. STRATTERA dosage: 18 MG, DAILY (1/D). During the same period patient was treated with MEDIKINET. Patient was hospitalized. Patient recovered.

STRATTERA problem was reported by a Physician from GERMANY on Mar 23, 2007. Male patient, child 12 years of age, weighting 114.4 lb, was diagnosed with attention deficit/hyperactivity disorder and was treated with STRATTERA. After drug was administered, patient experienced the following problems/side effects: intentional self-injury, suicidal ideation. STRATTERA dosage: 25 MG, EACH MORNING. Patient recovered.

Physician from UNITED KINGDOM reported STRATTERA problem on Mar 22, 2007. Male patient, child 10 years of age, was diagnosed with attention deficit/hyperactivity disorder and was treated with STRATTERA. After drug was administered, patient experienced the following problems/side effects: apathy, chills, diarrhoea, feeling cold, headache, influenza like illness, insomnia, pain in extremity, pollakiuria. STRATTERA dosage: 40 MG, UNK. During the same period patient was treated with EQUASYM, RISPERIDONE. Patient recovered.

STRATTERA problem was reported by a Physician from GERMANY on Mar 22, 2007. Male patient, 16 years of age, was diagnosed with attention deficit/hyperactivity disorder and was treated with STRATTERA. After drug was administered, patient experienced the following problems/side effects: blood alkaline phosphatase increased, blood bilirubin increased. STRATTERA dosage: 25 MG, 2/D. During the same period patient was treated with MEDIKINET. Patient recovered.

Physician from UNITED STATES reported STRATTERA problem on Mar 23, 2007. Male patient, child 7 years of age, weighting 44.09 lb, was diagnosed with attention deficit/hyperactivity disorder, sleep disorder and was treated with STRATTERA. After drug was administered, patient experienced the following problems/side effects: aggression, convulsion, prescribed overdose, pyromania, snoring, somnolence. STRATTERA dosage: 2 MG/KG, DAILY (1/D). During the same period patient was treated with ZOLOFT, RISPERDAL, MELATONIN. Patient was hospitalized. Patient recovered.

STRATTERA problem was reported by a Physician from NETHERLANDS on Mar 26, 2007. Male patient, 13 years of age, weighting 78.71 lb, was diagnosed with attention deficit/hyperactivity disorder, sleep disorder and was treated with STRATTERA. After drug was administered, patient experienced the following problems/side effects: arrhythmia, dyspnoea, exercise tolerance decreased, heart rate increased. STRATTERA dosage: 40 MG, UNK. During the same period patient was treated with MELATONIN. Patient recovered.

Physician from SWEDEN reported STRATTERA problem on Mar 26, 2007. Male patient, 14 years of age, was diagnosed with attention deficit/hyperactivity disorder and was treated with STRATTERA. After drug was administered, patient experienced the following problems/side effects: electrocardiogram qt prolonged, loss of consciousness. STRATTERA dosage: 40 MG, DAILY (1/D). Patient was hospitalized. Patient recovered.

STRATTERA problem was reported by a Physician from NORWAY on Mar 28, 2007. Male patient, 15 years of age, was diagnosed with attention deficit/hyperactivity disorder and was treated with STRATTERA. After drug was administered, patient experienced the following problems/side effects: alcohol poisoning, respiratory failure. STRATTERA dosage: unknown. During the same period patient was treated with RITALIN, ETHANOL. Patient was hospitalized. Patient recovered.

Physician from UNITED STATES reported STRATTERA problem on Mar 29, 2007. Male patient, 25 years of age, was diagnosed with attention deficit/hyperactivity disorder and was treated with STRATTERA. After drug was administered, patient experienced the following problems/side effects: alanine aminotransferase increased, aspartate aminotransferase increased, gilbert's syndrome, haematuria, hepatocellular damage, hyperbilirubinaemia. STRATTERA dosage: unknown. Patient recovered.

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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
EquetroThis drug has as active FDA Safety Alert (carbamazepine)
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
GadoliniumThis drug has as active FDA Safety Alert
Gadopentetate DimeglumineThis drug has as active FDA Safety Alert
GadoteridolThis drug has as active FDA Safety Alert
GadoversetamideThis drug has as active FDA Safety Alert
GalantamineThis drug has as active FDA Safety Alert
Ganirelix acetate
GatifloxacinThis drug has as active FDA Safety Alert
GefitinibThis drug has as active FDA Safety Alert
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
PamidronateThis drug has as active FDA Safety Alert
Panitumumab
Panretin Gel (alitretinoin)
Pantoprazole
Paricalcitol
ParoxetineThis drug has as active FDA Safety Alert
PaxilThis drug has as active FDA Safety Alert (paroxetine)
Pegaptanib
Pegvisomant

Pemetrexed
PemolineThis drug has as active FDA Safety Alert
Pentobarbital and carbromal
Perflutren lipid microspheres
PerindoprilThis drug has as active FDA Safety Alert
PhenerganThis drug has as active FDA Safety Alert (promethazine)
Pimecrolimus

PioglitazoneThis drug has as active FDA Safety Alert
Placidyl (ethchlorvynol)
Plan B (levonorgestrel)
Pletal (cilostazol)
Poractant alfa
Posaconazole
Pramlintide Acetate
Precedex (dexmedetomidine)
PregabalinThis drug has as active FDA Safety Alert
Prezista (darunavir)
Prialt (ziconotide)
Priftin (rifapentine)
Prinivil