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

DEPRESSION ( 34 FDA reports)
SOMNOLENCE ( 31 FDA reports)
CRYING ( 23 FDA reports)
PAIN IN EXTREMITY ( 23 FDA reports)
WEIGHT INCREASED ( 21 FDA reports)
INSOMNIA ( 20 FDA reports)
PAIN ( 20 FDA reports)
TREMOR ( 20 FDA reports)
DECREASED APPETITE ( 19 FDA reports)
DIZZINESS ( 19 FDA reports)
NAUSEA ( 19 FDA reports)
DRUG INEFFECTIVE ( 18 FDA reports)
HEADACHE ( 18 FDA reports)
SUICIDE ATTEMPT ( 18 FDA reports)
WEIGHT DECREASED ( 18 FDA reports)
BLOOD PRESSURE DECREASED ( 17 FDA reports)
ANXIETY ( 16 FDA reports)
CONFUSIONAL STATE ( 16 FDA reports)
NECK PAIN ( 16 FDA reports)
AGGRESSION ( 15 FDA reports)
HYPERSENSITIVITY ( 15 FDA reports)
IRRITABILITY ( 15 FDA reports)
FATIGUE ( 13 FDA reports)
HYPOAESTHESIA ( 13 FDA reports)
TACHYCARDIA ( 13 FDA reports)
ABDOMINAL PAIN ( 12 FDA reports)
AGITATION ( 12 FDA reports)
SHOCK ( 12 FDA reports)
VOMITING ( 12 FDA reports)
EUPHORIC MOOD ( 11 FDA reports)
MALAISE ( 11 FDA reports)
MENSTRUAL DISORDER ( 11 FDA reports)
MUSCULOSKELETAL PAIN ( 11 FDA reports)
ABORTION ( 10 FDA reports)
ALCOHOLISM ( 10 FDA reports)
AMENORRHOEA ( 10 FDA reports)
BIPOLAR DISORDER ( 10 FDA reports)
CONVULSION ( 10 FDA reports)
DYSKINESIA ( 10 FDA reports)
EYELID PTOSIS ( 10 FDA reports)
FORMICATION ( 10 FDA reports)
GALACTORRHOEA ( 10 FDA reports)
GRIP STRENGTH DECREASED ( 10 FDA reports)
HAEMORRHAGE ( 10 FDA reports)
HYPOTHYROIDISM ( 10 FDA reports)
INFLUENZA LIKE ILLNESS ( 10 FDA reports)
PHOBIA ( 10 FDA reports)
SEBORRHOEIC DERMATITIS ( 10 FDA reports)
SINUSITIS ( 10 FDA reports)
SKIN LESION ( 10 FDA reports)
VAGINAL INFECTION ( 10 FDA reports)
BREAST PAIN ( 9 FDA reports)
EATING DISORDER ( 9 FDA reports)
HALLUCINATION ( 9 FDA reports)
MULTIPLE SCLEROSIS RELAPSE ( 9 FDA reports)
ASTHENIA ( 8 FDA reports)
MOVEMENT DISORDER ( 8 FDA reports)
RHINITIS ( 8 FDA reports)
SUICIDAL IDEATION ( 8 FDA reports)
TENDONITIS ( 8 FDA reports)
URINARY INCONTINENCE ( 8 FDA reports)
HALLUCINATION, AUDITORY ( 7 FDA reports)
HALLUCINATIONS, MIXED ( 7 FDA reports)
PSYCHOTIC DISORDER ( 7 FDA reports)
STRESS ( 7 FDA reports)
BLOOD PRESSURE INCREASED ( 6 FDA reports)
BLOOD PROLACTIN INCREASED ( 6 FDA reports)
DEPRESSED LEVEL OF CONSCIOUSNESS ( 6 FDA reports)
DRUG LEVEL DECREASED ( 6 FDA reports)
FALL ( 6 FDA reports)
INFLUENZA ( 6 FDA reports)
MUSCLE SPASMS ( 6 FDA reports)
NERVOUSNESS ( 6 FDA reports)
ARTHRALGIA ( 5 FDA reports)
BLOOD CHOLESTEROL INCREASED ( 5 FDA reports)
BLOOD TRIGLYCERIDES INCREASED ( 5 FDA reports)
CONSTIPATION ( 5 FDA reports)
COORDINATION ABNORMAL ( 5 FDA reports)
DEEP VEIN THROMBOSIS ( 5 FDA reports)
DELUSION ( 5 FDA reports)
DEPRESSED MOOD ( 5 FDA reports)
FAECAL INCONTINENCE ( 5 FDA reports)
FEELING ABNORMAL ( 5 FDA reports)
HEPATIC PAIN ( 5 FDA reports)
HYPOTENSION ( 5 FDA reports)
IMMUNODEFICIENCY ( 5 FDA reports)
MOOD SWINGS ( 5 FDA reports)
PANIC ATTACK ( 5 FDA reports)
PANIC DISORDER ( 5 FDA reports)
PNEUMONIA ( 5 FDA reports)
PRURITUS ( 5 FDA reports)
PYROMANIA ( 5 FDA reports)
RASH ( 5 FDA reports)
REFLUX GASTRITIS ( 5 FDA reports)
SUFFOCATION FEELING ( 5 FDA reports)
SYNCOPE ( 5 FDA reports)
VIOLENCE-RELATED SYMPTOM ( 5 FDA reports)
WHITE BLOOD CELL COUNT INCREASED ( 5 FDA reports)
ABDOMINAL PAIN UPPER ( 4 FDA reports)
AMNESIA ( 4 FDA reports)
DRUG INTERACTION ( 4 FDA reports)
DYSPHONIA ( 4 FDA reports)
GAIT DISTURBANCE ( 4 FDA reports)
HYPERSOMNIA ( 4 FDA reports)
HYPERTENSION ( 4 FDA reports)
HYPOKINESIA ( 4 FDA reports)
MOTOR DYSFUNCTION ( 4 FDA reports)
MULTIPLE SCLEROSIS ( 4 FDA reports)
MYALGIA ( 4 FDA reports)
OXYGEN SATURATION DECREASED ( 4 FDA reports)
PALLOR ( 4 FDA reports)
PANIC REACTION ( 4 FDA reports)
PREMENSTRUAL SYNDROME ( 4 FDA reports)
QUADRIPARESIS ( 4 FDA reports)
RENAL FAILURE ( 4 FDA reports)
SEDATION ( 4 FDA reports)
SLEEP DISORDER ( 4 FDA reports)
VAGINAL CANDIDIASIS ( 4 FDA reports)
VISUAL ACUITY REDUCED ( 4 FDA reports)
VISUAL DISTURBANCE ( 4 FDA reports)
WITHDRAWAL SYNDROME ( 4 FDA reports)
ABASIA ( 3 FDA reports)
ABNORMAL BEHAVIOUR ( 3 FDA reports)
BLOOD PRESSURE FLUCTUATION ( 3 FDA reports)
DYSPNOEA ( 3 FDA reports)
EMOTIONAL DISORDER ( 3 FDA reports)
ERECTILE DYSFUNCTION ( 3 FDA reports)
FACIAL PAIN ( 3 FDA reports)
HEART RATE INCREASED ( 3 FDA reports)
INFECTION ( 3 FDA reports)
INTENTIONAL DRUG MISUSE ( 3 FDA reports)
LETHARGY ( 3 FDA reports)
LIBIDO DECREASED ( 3 FDA reports)
LOSS OF CONSCIOUSNESS ( 3 FDA reports)
MAJOR DEPRESSION ( 3 FDA reports)
MEDICATION ERROR ( 3 FDA reports)
MENTAL IMPAIRMENT ( 3 FDA reports)
MIGRAINE ( 3 FDA reports)
PRODUCT QUALITY ISSUE ( 3 FDA reports)
SCHIZOPHRENIA ( 3 FDA reports)
SELF INJURIOUS BEHAVIOUR ( 3 FDA reports)
SPEECH DISORDER ( 3 FDA reports)
THROAT IRRITATION ( 3 FDA reports)
TOOTH DISORDER ( 3 FDA reports)
URINARY TRACT INFECTION ( 3 FDA reports)
VISUAL FIELD DEFECT ( 3 FDA reports)
APNOEA ( 2 FDA reports)
ASTHENOPIA ( 2 FDA reports)
BLOOD GLUCOSE FLUCTUATION ( 2 FDA reports)
BRUXISM ( 2 FDA reports)
CARDIAC ARREST ( 2 FDA reports)
CARDIO-RESPIRATORY ARREST ( 2 FDA reports)
CHEST PAIN ( 2 FDA reports)
CIRCUMSTANCE OR INFORMATION CAPABLE OF LEADING TO MEDICATION ERROR ( 2 FDA reports)
COMA ( 2 FDA reports)
COUGH ( 2 FDA reports)
DRUG PRESCRIBING ERROR ( 2 FDA reports)
DRY MOUTH ( 2 FDA reports)
DYSARTHRIA ( 2 FDA reports)
DYSURIA ( 2 FDA reports)
EAR DISCOMFORT ( 2 FDA reports)
EJACULATION DISORDER ( 2 FDA reports)
GINGIVAL ABSCESS ( 2 FDA reports)
GRIMACING ( 2 FDA reports)
HALLUCINATION, VISUAL ( 2 FDA reports)
HEART RATE DECREASED ( 2 FDA reports)
HOARSENESS ( 2 FDA reports)
KERATITIS HERPETIC ( 2 FDA reports)
LEARNING DISORDER ( 2 FDA reports)
MANIA ( 2 FDA reports)
MEMORY IMPAIRMENT ( 2 FDA reports)
MENTAL DISORDER ( 2 FDA reports)
MOOD ALTERED ( 2 FDA reports)
MULTI-ORGAN FAILURE ( 2 FDA reports)
MUSCULAR WEAKNESS ( 2 FDA reports)
NEURALGIA ( 2 FDA reports)
OVERDOSE ( 2 FDA reports)
POOR QUALITY SLEEP ( 2 FDA reports)
POST-TRAUMATIC STRESS DISORDER ( 2 FDA reports)
PYREXIA ( 2 FDA reports)
RESPIRATORY ARREST ( 2 FDA reports)
RESPIRATORY FAILURE ( 2 FDA reports)
RESTLESSNESS ( 2 FDA reports)
SENSORY LOSS ( 2 FDA reports)
SKIN NECROSIS ( 2 FDA reports)
SWOLLEN TONGUE ( 2 FDA reports)
THERAPEUTIC PRODUCT INEFFECTIVE ( 2 FDA reports)
THOUGHT BLOCKING ( 2 FDA reports)
ABNORMAL SLEEP-RELATED EVENT ( 1 FDA reports)
ACARODERMATITIS ( 1 FDA reports)
ACCIDENTAL OVERDOSE ( 1 FDA reports)
ACUTE PSYCHOSIS ( 1 FDA reports)
AFFECT LABILITY ( 1 FDA reports)
ALOPECIA ( 1 FDA reports)
ANAL HAEMORRHAGE ( 1 FDA reports)
ANOREXIA ( 1 FDA reports)
ANTICONVULSANT DRUG LEVEL DECREASED ( 1 FDA reports)
ARRHYTHMIA ( 1 FDA reports)
ASEPTIC NECROSIS BONE ( 1 FDA reports)
ATROPHIC VULVOVAGINITIS ( 1 FDA reports)
BACK PAIN ( 1 FDA reports)
BILIARY COLIC ( 1 FDA reports)
BLADDER DILATATION ( 1 FDA reports)
BLOOD GLUCOSE DECREASED ( 1 FDA reports)
BLOOD POTASSIUM DECREASED ( 1 FDA reports)
BONE DEBRIDEMENT ( 1 FDA reports)
BONE EROSION ( 1 FDA reports)
BONE TRIMMING ( 1 FDA reports)
BRONCHITIS ( 1 FDA reports)
CARDIAC DISCOMFORT ( 1 FDA reports)
CEREBRAL HAEMORRHAGE ( 1 FDA reports)
CEREBRAL ISCHAEMIA ( 1 FDA reports)
CHEST DISCOMFORT ( 1 FDA reports)
CHILLS ( 1 FDA reports)
COLD SWEAT ( 1 FDA reports)
DEATH ( 1 FDA reports)
DECREASED INTEREST ( 1 FDA reports)
DEHYDRATION ( 1 FDA reports)
DELIRIUM ( 1 FDA reports)
DEPOSIT EYE ( 1 FDA reports)
DIABETES MELLITUS ( 1 FDA reports)
DIPLOPIA ( 1 FDA reports)
DRUG DEPENDENCE ( 1 FDA reports)
DRUG HYPERSENSITIVITY ( 1 FDA reports)
DYSGEUSIA ( 1 FDA reports)
DYSPEPSIA ( 1 FDA reports)
DYSPHAGIA ( 1 FDA reports)
EAR PAIN ( 1 FDA reports)
ELECTRIC SHOCK ( 1 FDA reports)
EMOTIONAL DISTRESS ( 1 FDA reports)
EPISTAXIS ( 1 FDA reports)
ERYTHEMA ( 1 FDA reports)
EYE LASER SURGERY ( 1 FDA reports)
EYE LUXATION ( 1 FDA reports)
EYE PAIN ( 1 FDA reports)
FEEDING DISORDER ( 1 FDA reports)
FEELING COLD ( 1 FDA reports)
FEMUR FRACTURE ( 1 FDA reports)
FLUSHING ( 1 FDA reports)
GLOSSODYNIA ( 1 FDA reports)
HAEMATURIA ( 1 FDA reports)
HEAD DISCOMFORT ( 1 FDA reports)
HEPATIC ENZYME ABNORMAL ( 1 FDA reports)
HEPATIC NEOPLASM MALIGNANT ( 1 FDA reports)
HEPATOMEGALY ( 1 FDA reports)
HOSPITALISATION ( 1 FDA reports)
HUNGER ( 1 FDA reports)
HYPERGLYCAEMIA ( 1 FDA reports)
HYPERHIDROSIS ( 1 FDA reports)
INFUSION RELATED REACTION ( 1 FDA reports)
INJECTION SITE ERYTHEMA ( 1 FDA reports)
INJECTION SITE HAEMATOMA ( 1 FDA reports)
INJECTION SITE MASS ( 1 FDA reports)
INTENTIONAL OVERDOSE ( 1 FDA reports)
INTENTIONAL SELF-INJURY ( 1 FDA reports)
INTERVERTEBRAL DISC INJURY ( 1 FDA reports)
IRON DEFICIENCY ANAEMIA ( 1 FDA reports)
LABYRINTHITIS ( 1 FDA reports)
LISTLESS ( 1 FDA reports)
LOCAL SWELLING ( 1 FDA reports)
LUNG INFILTRATION ( 1 FDA reports)
MALIGNANT NEOPLASM PROGRESSION ( 1 FDA reports)
MEDICAL DEVICE IMPLANTATION ( 1 FDA reports)
MENOPAUSE ( 1 FDA reports)
MOBILITY DECREASED ( 1 FDA reports)
MONOPLEGIA ( 1 FDA reports)
NEOPLASM ( 1 FDA reports)
NERVOUS SYSTEM DISORDER ( 1 FDA reports)
NO THERAPEUTIC RESPONSE ( 1 FDA reports)
OBSESSIVE THOUGHTS ( 1 FDA reports)
OFF LABEL USE ( 1 FDA reports)
OOPHORITIS ( 1 FDA reports)
OROPHARYNGEAL PAIN ( 1 FDA reports)
PALPITATIONS ( 1 FDA reports)
PARAESTHESIA ( 1 FDA reports)
PARAESTHESIA ORAL ( 1 FDA reports)
PERSECUTORY DELUSION ( 1 FDA reports)
PHYSICAL ABUSE ( 1 FDA reports)
PLATELET COUNT ABNORMAL ( 1 FDA reports)
PLATELET COUNT DECREASED ( 1 FDA reports)
PROCEDURAL COMPLICATION ( 1 FDA reports)
PROCEDURAL PAIN ( 1 FDA reports)
PROGRESSIVE MULTIPLE SCLEROSIS ( 1 FDA reports)
PROSTHESIS USER ( 1 FDA reports)
RHEUMATOID ARTHRITIS ( 1 FDA reports)
SALIVARY HYPERSECRETION ( 1 FDA reports)
SCAB ( 1 FDA reports)
SCREAMING ( 1 FDA reports)
SENSATION OF HEAVINESS ( 1 FDA reports)
SENSORY DISTURBANCE ( 1 FDA reports)
SNORING ( 1 FDA reports)
SOLILOQUY ( 1 FDA reports)
SOMNAMBULISM ( 1 FDA reports)
SPINAL CORD DISORDER ( 1 FDA reports)
SPINAL PAIN ( 1 FDA reports)
STARING ( 1 FDA reports)
STOMATITIS ( 1 FDA reports)
STRABISMUS ( 1 FDA reports)
THROMBOCYTOPENIA ( 1 FDA reports)
TOOTH EXTRACTION ( 1 FDA reports)
TOOTH INJURY ( 1 FDA reports)
TOXICITY TO VARIOUS AGENTS ( 1 FDA reports)
TRANSPLANT ( 1 FDA reports)
TUBERCULOSIS ( 1 FDA reports)
UNDERWEIGHT ( 1 FDA reports)
UNEVALUABLE EVENT ( 1 FDA reports)
URINARY RETENTION ( 1 FDA reports)
VAGINAL HAEMORRHAGE ( 1 FDA reports)
VERBAL ABUSE ( 1 FDA reports)
VULVOVAGINAL BURNING SENSATION ( 1 FDA reports)

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