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

VOMITING ( 5 FDA reports)
DRUG INTERACTION ( 4 FDA reports)
FEELING ABNORMAL ( 4 FDA reports)
HYPOTENSION ( 4 FDA reports)
MALAISE ( 4 FDA reports)
TACHYCARDIA ( 4 FDA reports)
ABDOMINAL PAIN ( 3 FDA reports)
CARDIAC ARREST ( 3 FDA reports)
COMPLETED SUICIDE ( 3 FDA reports)
CONVULSION ( 3 FDA reports)
DEHYDRATION ( 3 FDA reports)
DIZZINESS ( 3 FDA reports)
FALL ( 3 FDA reports)
MULTIPLE DRUG OVERDOSE ( 3 FDA reports)
PYREXIA ( 3 FDA reports)
URTICARIA ( 3 FDA reports)
ACCIDENT ( 2 FDA reports)
AGGRESSION ( 2 FDA reports)
AMNESIA ( 2 FDA reports)
ANAEMIA ( 2 FDA reports)
ANURIA ( 2 FDA reports)
ATRIAL FIBRILLATION ( 2 FDA reports)
BLINDNESS UNILATERAL ( 2 FDA reports)
BLOOD PRESSURE FLUCTUATION ( 2 FDA reports)
BLOOD PRESSURE INCREASED ( 2 FDA reports)
CARDIAC FAILURE ( 2 FDA reports)
CEREBRAL HAEMORRHAGE ( 2 FDA reports)
CIRCADIAN RHYTHM SLEEP DISORDER ( 2 FDA reports)
CONFUSIONAL STATE ( 2 FDA reports)
CROHN'S DISEASE ( 2 FDA reports)
DRUG HYPERSENSITIVITY ( 2 FDA reports)
DYSURIA ( 2 FDA reports)
EYE HAEMORRHAGE ( 2 FDA reports)
HAEMODIALYSIS ( 2 FDA reports)
HEMIPARESIS ( 2 FDA reports)
HYPERSENSITIVITY ( 2 FDA reports)
HYPERSOMNIA ( 2 FDA reports)
HYPERTENSION ( 2 FDA reports)
ILEUS ( 2 FDA reports)
INFUSION RELATED REACTION ( 2 FDA reports)
INSOMNIA ( 2 FDA reports)
LIVER FUNCTION TEST ABNORMAL ( 2 FDA reports)
LOWER RESPIRATORY TRACT INFECTION ( 2 FDA reports)
LUPUS-LIKE SYNDROME ( 2 FDA reports)
MYOCARDIAL INFARCTION ( 2 FDA reports)
NIGHT BLINDNESS ( 2 FDA reports)
PAIN ( 2 FDA reports)
PANIC REACTION ( 2 FDA reports)
PHARMACEUTICAL PRODUCT COMPLAINT ( 2 FDA reports)
PLATELET COUNT DECREASED ( 2 FDA reports)
RASH PRURITIC ( 2 FDA reports)
REFUSAL OF TREATMENT BY PATIENT ( 2 FDA reports)
RENAL DISORDER ( 2 FDA reports)
SEPSIS ( 2 FDA reports)
SHOCK ( 2 FDA reports)
SINUSITIS ( 2 FDA reports)
SMALL INTESTINAL OBSTRUCTION ( 2 FDA reports)
STEVENS-JOHNSON SYNDROME ( 2 FDA reports)
SUDDEN CARDIAC DEATH ( 2 FDA reports)
SWOLLEN TONGUE ( 2 FDA reports)
THERAPY NON-RESPONDER ( 2 FDA reports)
TREMOR ( 2 FDA reports)
URINARY TRACT INFECTION ( 2 FDA reports)
URINE OUTPUT DECREASED ( 2 FDA reports)
VASODILATATION ( 2 FDA reports)
VIRAL INFECTION ( 2 FDA reports)
VISUAL DISTURBANCE ( 2 FDA reports)
WHITE BLOOD CELL COUNT DECREASED ( 2 FDA reports)
ABDOMINAL PAIN LOWER ( 1 FDA reports)
ADNEXA UTERI MASS ( 1 FDA reports)
ADRENOCORTICAL INSUFFICIENCY ACUTE ( 1 FDA reports)
ALCOHOL USE ( 1 FDA reports)
ANGIONEUROTIC OEDEMA ( 1 FDA reports)
ANXIETY ( 1 FDA reports)
ARTHRITIS ( 1 FDA reports)
ARTHROPATHY ( 1 FDA reports)
ARTHROPOD BITE ( 1 FDA reports)
ASTHENIA ( 1 FDA reports)
BACK DISORDER ( 1 FDA reports)
BLOOD POTASSIUM DECREASED ( 1 FDA reports)
BLOOD PRESSURE DECREASED ( 1 FDA reports)
BLOOD PRESSURE IMMEASURABLE ( 1 FDA reports)
BLOOD UREA INCREASED ( 1 FDA reports)
C-REACTIVE PROTEIN INCREASED ( 1 FDA reports)
CANDIDIASIS ( 1 FDA reports)
CARDIAC DEATH ( 1 FDA reports)
CARDIOMEGALY ( 1 FDA reports)
CATHETER RELATED INFECTION ( 1 FDA reports)
CELLULITIS ( 1 FDA reports)
CEREBROVASCULAR ACCIDENT ( 1 FDA reports)
CHEST DISCOMFORT ( 1 FDA reports)
CHEST PAIN ( 1 FDA reports)
CLONUS ( 1 FDA reports)
COMA ( 1 FDA reports)
DEATH ( 1 FDA reports)
DEPRESSION ( 1 FDA reports)
DERMATITIS ALLERGIC ( 1 FDA reports)
DIARRHOEA ( 1 FDA reports)
DRUG EFFECT DECREASED ( 1 FDA reports)
DRUG INEFFECTIVE ( 1 FDA reports)
DYSPEPSIA ( 1 FDA reports)
DYSPHAGIA ( 1 FDA reports)
DYSPNOEA ( 1 FDA reports)
DYSTONIA ( 1 FDA reports)
ELECTROCARDIOGRAM QT PROLONGED ( 1 FDA reports)
ENURESIS ( 1 FDA reports)
ERUCTATION ( 1 FDA reports)
ERYTHEMA MULTIFORME ( 1 FDA reports)
FACIAL PALSY ( 1 FDA reports)
FIBROSIS ( 1 FDA reports)
FISTULA ( 1 FDA reports)
GASTROOESOPHAGEAL REFLUX DISEASE ( 1 FDA reports)
HALLUCINATION ( 1 FDA reports)
HALLUCINATION, VISUAL ( 1 FDA reports)
HALLUCINATIONS, MIXED ( 1 FDA reports)
HEADACHE ( 1 FDA reports)
HEART RATE INCREASED ( 1 FDA reports)
HIP FRACTURE ( 1 FDA reports)
HYPERHIDROSIS ( 1 FDA reports)
HYPERVENTILATION ( 1 FDA reports)
HYSTERECTOMY ( 1 FDA reports)
INTENTIONAL OVERDOSE ( 1 FDA reports)
IRRITABLE BOWEL SYNDROME ( 1 FDA reports)
KIDNEY INFECTION ( 1 FDA reports)
KNEE ARTHROPLASTY ( 1 FDA reports)
LABORATORY TEST ABNORMAL ( 1 FDA reports)
MANTLE CELL LYMPHOMA RECURRENT ( 1 FDA reports)
METABOLIC ACIDOSIS ( 1 FDA reports)
MIGRAINE ( 1 FDA reports)
MOUTH ULCERATION ( 1 FDA reports)
MULTIPLE ALLERGIES ( 1 FDA reports)
MUSCLE SPASMS ( 1 FDA reports)
MUSCULOSKELETAL STIFFNESS ( 1 FDA reports)
MYALGIA ( 1 FDA reports)
NASOPHARYNGITIS ( 1 FDA reports)
NAUSEA ( 1 FDA reports)
NERVE COMPRESSION ( 1 FDA reports)
OCULAR HYPERAEMIA ( 1 FDA reports)
OEDEMA PERIPHERAL ( 1 FDA reports)
OROPHARYNGEAL SWELLING ( 1 FDA reports)
PAIN IN EXTREMITY ( 1 FDA reports)
PANCYTOPENIA ( 1 FDA reports)
PANIC ATTACK ( 1 FDA reports)
PELVIC FRACTURE ( 1 FDA reports)
PNEUMONIA KLEBSIELLA ( 1 FDA reports)
POLYARTHRITIS ( 1 FDA reports)
POLYP ( 1 FDA reports)
POLYPECTOMY ( 1 FDA reports)
PROSTATE CANCER ( 1 FDA reports)
PROSTRATION ( 1 FDA reports)
PRURITUS ( 1 FDA reports)
RASH ( 1 FDA reports)
RENAL IMPAIRMENT ( 1 FDA reports)
RESPIRATORY ARREST ( 1 FDA reports)
RIB FRACTURE ( 1 FDA reports)
SACRAL PAIN ( 1 FDA reports)
SELF-MEDICATION ( 1 FDA reports)
SENSORY DISTURBANCE ( 1 FDA reports)
SOMNOLENCE ( 1 FDA reports)
SPINAL COLUMN STENOSIS ( 1 FDA reports)
SUDDEN DEATH ( 1 FDA reports)
SUICIDAL IDEATION ( 1 FDA reports)
SWELLING ( 1 FDA reports)
SYNCOPE ( 1 FDA reports)
SYSTEMIC LUPUS ERYTHEMATOSUS ( 1 FDA reports)
THERAPEUTIC RESPONSE DELAYED ( 1 FDA reports)
TOOTH ABSCESS ( 1 FDA reports)
TREATMENT NONCOMPLIANCE ( 1 FDA reports)
ULCER ( 1 FDA reports)
UTERINE NEOPLASM ( 1 FDA reports)
VENTRICULAR EXTRASYSTOLES ( 1 FDA reports)
WEIGHT DECREASED ( 1 FDA reports)
WEIGHT FLUCTUATION ( 1 FDA reports)
WHEEZING ( 1 FDA reports)

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