Please choose an event type to view the corresponding MedsFacts report:

SUICIDAL IDEATION ( 7 FDA reports)
CONFUSIONAL STATE ( 6 FDA reports)
WEIGHT INCREASED ( 6 FDA reports)
DRUG DOSE OMISSION ( 5 FDA reports)
AGITATION ( 4 FDA reports)
DEPRESSION ( 4 FDA reports)
DIZZINESS ( 4 FDA reports)
PSYCHOTIC DISORDER ( 4 FDA reports)
AGGRESSION ( 3 FDA reports)
ANGER ( 3 FDA reports)
BLOOD PRESSURE INCREASED ( 3 FDA reports)
COUGH ( 3 FDA reports)
FEELING ABNORMAL ( 3 FDA reports)
HEADACHE ( 3 FDA reports)
MYALGIA ( 3 FDA reports)
OVERDOSE ( 3 FDA reports)
PARANOIA ( 3 FDA reports)
SEDATION ( 3 FDA reports)
AFFECTIVE DISORDER ( 2 FDA reports)
ANXIETY ( 2 FDA reports)
BREAST CANCER ( 2 FDA reports)
CONDITION AGGRAVATED ( 2 FDA reports)
CONVULSION ( 2 FDA reports)
DECREASED APPETITE ( 2 FDA reports)
DISORIENTATION ( 2 FDA reports)
DRUG ADMINISTRATION ERROR ( 2 FDA reports)
DRUG INEFFECTIVE ( 2 FDA reports)
DRUG INTERACTION ( 2 FDA reports)
HALLUCINATION ( 2 FDA reports)
HYPOTENSION ( 2 FDA reports)
IMPAIRED DRIVING ABILITY ( 2 FDA reports)
INSOMNIA ( 2 FDA reports)
MANIA ( 2 FDA reports)
MENTAL STATUS CHANGES ( 2 FDA reports)
MOOD ALTERED ( 2 FDA reports)
MUSCLE TWITCHING ( 2 FDA reports)
NAUSEA ( 2 FDA reports)
PAIN IN EXTREMITY ( 2 FDA reports)
PNEUMONIA ( 2 FDA reports)
PYREXIA ( 2 FDA reports)
RENAL FAILURE ACUTE ( 2 FDA reports)
SEROTONIN SYNDROME ( 2 FDA reports)
SEXUAL DYSFUNCTION ( 2 FDA reports)
WHITE BLOOD CELL COUNT INCREASED ( 2 FDA reports)
WITHDRAWAL SYNDROME ( 2 FDA reports)
ABDOMINAL ABSCESS ( 1 FDA reports)
ABNORMAL BEHAVIOUR ( 1 FDA reports)
ADRENAL MASS ( 1 FDA reports)
AKATHISIA ( 1 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 1 FDA reports)
ALOPECIA ( 1 FDA reports)
ANAEMIA ( 1 FDA reports)
ANTICONVULSANT DRUG LEVEL DECREASED ( 1 FDA reports)
ARTHRALGIA ( 1 FDA reports)
ARTHROPATHY ( 1 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 1 FDA reports)
ASTHENIA ( 1 FDA reports)
AUTONOMIC NERVOUS SYSTEM IMBALANCE ( 1 FDA reports)
AUTONOMIC NEUROPATHY ( 1 FDA reports)
BACK PAIN ( 1 FDA reports)
BLOOD GLUCOSE DECREASED ( 1 FDA reports)
BLOOD SODIUM DECREASED ( 1 FDA reports)
BRADYCARDIA ( 1 FDA reports)
BREAST NEOPLASM ( 1 FDA reports)
C-REACTIVE PROTEIN INCREASED ( 1 FDA reports)
CHEST PAIN ( 1 FDA reports)
CHOLELITHIASIS ( 1 FDA reports)
CRYING ( 1 FDA reports)
CULTURE STOOL POSITIVE ( 1 FDA reports)
DEPENDENCE ( 1 FDA reports)
DEPRESSED LEVEL OF CONSCIOUSNESS ( 1 FDA reports)
DISSOCIATIVE IDENTITY DISORDER ( 1 FDA reports)
DIVERTICULUM ( 1 FDA reports)
DRUG DIVERSION ( 1 FDA reports)
DRUG EFFECT DECREASED ( 1 FDA reports)
DRUG EXPOSURE DURING PREGNANCY ( 1 FDA reports)
DRUG HYPERSENSITIVITY ( 1 FDA reports)
DRUG LEVEL BELOW THERAPEUTIC ( 1 FDA reports)
DRUG WITHDRAWAL SYNDROME ( 1 FDA reports)
DYSGRAPHIA ( 1 FDA reports)
DYSKINESIA ( 1 FDA reports)
DYSPHAGIA ( 1 FDA reports)
DYSTONIA ( 1 FDA reports)
ELECTROCARDIOGRAM QT PROLONGED ( 1 FDA reports)
EMOTIONAL DISORDER ( 1 FDA reports)
ENURESIS ( 1 FDA reports)
FAECAL INCONTINENCE ( 1 FDA reports)
FALL ( 1 FDA reports)
GAIT DISTURBANCE ( 1 FDA reports)
GALACTORRHOEA ( 1 FDA reports)
GLOMERULAR FILTRATION RATE DECREASED ( 1 FDA reports)
GLYCOSYLATED HAEMOGLOBIN INCREASED ( 1 FDA reports)
HAEMATOMA ( 1 FDA reports)
HAEMOPTYSIS ( 1 FDA reports)
HAEMORRHAGE ( 1 FDA reports)
HALLUCINATION, AUDITORY ( 1 FDA reports)
HEPATIC ENZYME INCREASED ( 1 FDA reports)
HEPATIC FAILURE ( 1 FDA reports)
HEPATIC STEATOSIS ( 1 FDA reports)
HOT FLUSH ( 1 FDA reports)
HYPERHIDROSIS ( 1 FDA reports)
HYPERNATRAEMIA ( 1 FDA reports)
HYPOAESTHESIA ( 1 FDA reports)
HYPOAESTHESIA ORAL ( 1 FDA reports)
HYPOKALAEMIA ( 1 FDA reports)
HYPONATRAEMIA ( 1 FDA reports)
HYPOPHAGIA ( 1 FDA reports)
INAPPROPRIATE SCHEDULE OF DRUG ADMINISTRATION ( 1 FDA reports)
INFECTIOUS PERITONITIS ( 1 FDA reports)
INFLUENZA LIKE ILLNESS ( 1 FDA reports)
INITIAL INSOMNIA ( 1 FDA reports)
INTENTIONAL OVERDOSE ( 1 FDA reports)
INTENTIONAL SELF-INJURY ( 1 FDA reports)
IRRITABILITY ( 1 FDA reports)
LABILE BLOOD PRESSURE ( 1 FDA reports)
LACERATION ( 1 FDA reports)
LETHARGY ( 1 FDA reports)
LEUKAEMIA ( 1 FDA reports)
LIVER DISORDER ( 1 FDA reports)
LIVER FUNCTION TEST ABNORMAL ( 1 FDA reports)
LYMPHADENOPATHY MEDIASTINAL ( 1 FDA reports)
MEDICATION RESIDUE ( 1 FDA reports)
MENSTRUATION IRREGULAR ( 1 FDA reports)
MESENTERIC LYMPHADENOPATHY ( 1 FDA reports)
MICTURITION URGENCY ( 1 FDA reports)
MIDDLE INSOMNIA ( 1 FDA reports)
MIGRAINE ( 1 FDA reports)
MUSCLE SPASMS ( 1 FDA reports)
NASOPHARYNGITIS ( 1 FDA reports)
NECK PAIN ( 1 FDA reports)
NEUTROPHIL COUNT INCREASED ( 1 FDA reports)
NIGHT SWEATS ( 1 FDA reports)
OESOPHAGITIS ( 1 FDA reports)
OROPHARYNGEAL PAIN ( 1 FDA reports)
ORTHOSTATIC HYPOTENSION ( 1 FDA reports)
OVARIAN CANCER ( 1 FDA reports)
PAIN ( 1 FDA reports)
PAIN IN JAW ( 1 FDA reports)
PALPITATIONS ( 1 FDA reports)
PERICARDIAL EFFUSION ( 1 FDA reports)
POLYCYSTIC OVARIES ( 1 FDA reports)
POOR QUALITY SLEEP ( 1 FDA reports)
POST-TRAUMATIC STRESS DISORDER ( 1 FDA reports)
PSORIATIC ARTHROPATHY ( 1 FDA reports)
PSYCHIATRIC SYMPTOM ( 1 FDA reports)
PSYCHOLOGICAL TRAUMA ( 1 FDA reports)
PSYCHOMOTOR HYPERACTIVITY ( 1 FDA reports)
PULMONARY FIBROSIS ( 1 FDA reports)
PULMONARY MASS ( 1 FDA reports)
RENAL CYST ( 1 FDA reports)
RENAL IMPAIRMENT ( 1 FDA reports)
RHEUMATOID ARTHRITIS ( 1 FDA reports)
SCHIZOPHRENIA, DISORGANISED TYPE ( 1 FDA reports)
SELF INJURIOUS BEHAVIOUR ( 1 FDA reports)
SINUS TACHYCARDIA ( 1 FDA reports)
SLEEP APNOEA SYNDROME ( 1 FDA reports)
SOMNOLENCE ( 1 FDA reports)
SPEECH DISORDER ( 1 FDA reports)
SPINAL COLUMN STENOSIS ( 1 FDA reports)
SPINAL OSTEOARTHRITIS ( 1 FDA reports)
SPLENIC CYST ( 1 FDA reports)
STEVENS-JOHNSON SYNDROME ( 1 FDA reports)
SUICIDE ATTEMPT ( 1 FDA reports)
SYNCOPE ( 1 FDA reports)
SYSTEMIC LUPUS ERYTHEMATOSUS ( 1 FDA reports)
TACHYCARDIA ( 1 FDA reports)
TARDIVE DYSKINESIA ( 1 FDA reports)
THERAPEUTIC RESPONSE DECREASED ( 1 FDA reports)
THINKING ABNORMAL ( 1 FDA reports)
TREMOR ( 1 FDA reports)
UNEVALUABLE EVENT ( 1 FDA reports)
UPPER GASTROINTESTINAL HAEMORRHAGE ( 1 FDA reports)
URINARY HESITATION ( 1 FDA reports)
URINARY TRACT INFECTION ( 1 FDA reports)
VITAMIN D DEFICIENCY ( 1 FDA reports)
WRONG TECHNIQUE IN DRUG USAGE PROCESS ( 1 FDA reports)

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