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

HAEMATOCRIT DECREASED ( 3 FDA reports)
DRUG EXPOSURE DURING PREGNANCY ( 2 FDA reports)
HAEMOGLOBIN DECREASED ( 2 FDA reports)
PNEUMONIA ( 2 FDA reports)
PULMONARY EMBOLISM ( 2 FDA reports)
TACHYCARDIA ( 2 FDA reports)
URINARY INCONTINENCE ( 2 FDA reports)
ABDOMINAL PAIN UPPER ( 1 FDA reports)
ACTIVITIES OF DAILY LIVING IMPAIRED ( 1 FDA reports)
AGITATION ( 1 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 1 FDA reports)
ALOPECIA ( 1 FDA reports)
ANTEPARTUM HAEMORRHAGE ( 1 FDA reports)
APPLICATION SITE REACTION ( 1 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 1 FDA reports)
ASTHENIA ( 1 FDA reports)
ASTHMA ( 1 FDA reports)
BACK PAIN ( 1 FDA reports)
BACTERIAL INFECTION ( 1 FDA reports)
BLINDNESS ( 1 FDA reports)
BLINDNESS UNILATERAL ( 1 FDA reports)
BLOOD ALBUMIN DECREASED ( 1 FDA reports)
BLOOD AMYLASE DECREASED ( 1 FDA reports)
BLOOD BICARBONATE INCREASED ( 1 FDA reports)
BLOOD CHLORIDE DECREASED ( 1 FDA reports)
BLOOD FIBRINOGEN INCREASED ( 1 FDA reports)
BLOOD GLUCOSE INCREASED ( 1 FDA reports)
BLOOD SODIUM DECREASED ( 1 FDA reports)
BLOOD TRIGLYCERIDES INCREASED ( 1 FDA reports)
BRONCHITIS ( 1 FDA reports)
CELLULITIS ( 1 FDA reports)
CHLOROPSIA ( 1 FDA reports)
COLD AGGLUTININS POSITIVE ( 1 FDA reports)
CONVULSION ( 1 FDA reports)
DEMYELINATION ( 1 FDA reports)
DIABETES MELLITUS ( 1 FDA reports)
DIPLEGIA ( 1 FDA reports)
DISCOMFORT ( 1 FDA reports)
DIZZINESS ( 1 FDA reports)
ENCEPHALITIS ( 1 FDA reports)
ENDOMETRIAL CANCER ( 1 FDA reports)
ENTERITIS INFECTIOUS ( 1 FDA reports)
ESCHERICHIA INFECTION ( 1 FDA reports)
EYE DISCHARGE ( 1 FDA reports)
FAECAL INCONTINENCE ( 1 FDA reports)
FALL ( 1 FDA reports)
FEELING ABNORMAL ( 1 FDA reports)
GASTROOESOPHAGEAL REFLUX DISEASE ( 1 FDA reports)
GENERAL PHYSICAL HEALTH DETERIORATION ( 1 FDA reports)
GUILLAIN-BARRE SYNDROME ( 1 FDA reports)
GUN SHOT WOUND ( 1 FDA reports)
HAEMOLYTIC ANAEMIA ( 1 FDA reports)
HEAD INJURY ( 1 FDA reports)
HEADACHE ( 1 FDA reports)
HEPATIC ENZYME INCREASED ( 1 FDA reports)
HYPERTENSION ( 1 FDA reports)
HYPOGLYCAEMIC SEIZURE ( 1 FDA reports)
HYPOTENSION ( 1 FDA reports)
HYPOTHYROIDISM ( 1 FDA reports)
INCORRECT STORAGE OF DRUG ( 1 FDA reports)
INFUSION RELATED REACTION ( 1 FDA reports)
INITIAL INSOMNIA ( 1 FDA reports)
INTENTIONAL SELF-INJURY ( 1 FDA reports)
INTERNATIONAL NORMALISED RATIO DECREASED ( 1 FDA reports)
IRRITABILITY ( 1 FDA reports)
KLEBSIELLA INFECTION ( 1 FDA reports)
MENINGITIS VIRAL ( 1 FDA reports)
MENORRHAGIA ( 1 FDA reports)
MENTAL STATUS CHANGES ( 1 FDA reports)
MUSCLE ATROPHY ( 1 FDA reports)
MUSCULOSKELETAL CHEST PAIN ( 1 FDA reports)
MUSCULOSKELETAL PAIN ( 1 FDA reports)
NASOPHARYNGITIS ( 1 FDA reports)
NAUSEA ( 1 FDA reports)
NECK PAIN ( 1 FDA reports)
NERVOUS SYSTEM DISORDER ( 1 FDA reports)
NEUTROPHIL PERCENTAGE INCREASED ( 1 FDA reports)
NUCLEAR MAGNETIC RESONANCE IMAGING BRAIN ABNORMAL ( 1 FDA reports)
OCULAR ICTERUS ( 1 FDA reports)
OEDEMA PERIPHERAL ( 1 FDA reports)
OPTIC ATROPHY ( 1 FDA reports)
OPTIC ISCHAEMIC NEUROPATHY ( 1 FDA reports)
OPTIC NEURITIS ( 1 FDA reports)
OTITIS MEDIA ( 1 FDA reports)
PAIN IN EXTREMITY ( 1 FDA reports)
PERIODIC LIMB MOVEMENT DISORDER ( 1 FDA reports)
PERIPHERAL SENSORY NEUROPATHY ( 1 FDA reports)
PHOTOPHOBIA ( 1 FDA reports)
PHYSICAL ASSAULT ( 1 FDA reports)
PLATELET COUNT DECREASED ( 1 FDA reports)
PNEUMONITIS ( 1 FDA reports)
PNEUMOTHORAX ( 1 FDA reports)
POOR QUALITY SLEEP ( 1 FDA reports)
PREGNANCY ( 1 FDA reports)
PREGNANCY WITH CONTRACEPTIVE DEVICE ( 1 FDA reports)
PROTHROMBIN TIME PROLONGED ( 1 FDA reports)
PRURITUS ( 1 FDA reports)
PURULENT DISCHARGE ( 1 FDA reports)
PYREXIA ( 1 FDA reports)
RADICULITIS ( 1 FDA reports)
RASH ( 1 FDA reports)
RASH GENERALISED ( 1 FDA reports)
RED BLOOD CELL COUNT DECREASED ( 1 FDA reports)
RENAL FAILURE ( 1 FDA reports)
SCLEROMALACIA ( 1 FDA reports)
SCOTOMA ( 1 FDA reports)
SELF-MEDICATION ( 1 FDA reports)
SEPSIS ( 1 FDA reports)
SKIN LESION ( 1 FDA reports)
SNORING ( 1 FDA reports)
SOMNOLENCE ( 1 FDA reports)
SUBDURAL HAEMATOMA ( 1 FDA reports)
THROMBOPHLEBITIS SUPERFICIAL ( 1 FDA reports)
TRAUMATIC BRAIN INJURY ( 1 FDA reports)
TREMOR ( 1 FDA reports)
URINARY TRACT INFECTION ( 1 FDA reports)
URINE OUTPUT DECREASED ( 1 FDA reports)
UTERINE LEIOMYOMA ( 1 FDA reports)
VAGINAL HAEMORRHAGE ( 1 FDA reports)
VERTIGO ( 1 FDA reports)
VISION BLURRED ( 1 FDA reports)
VISUAL FIELD DEFECT ( 1 FDA reports)
VOMITING ( 1 FDA reports)
WEIGHT DECREASED ( 1 FDA reports)
WHITE BLOOD CELL COUNT DECREASED ( 1 FDA reports)
XANTHOPSIA ( 1 FDA reports)

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