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

HEADACHE ( 12 FDA reports)
PULMONARY EMBOLISM ( 11 FDA reports)
BRONCHITIS ( 9 FDA reports)
DECREASED APPETITE ( 9 FDA reports)
GASTROENTERITIS ( 9 FDA reports)
MIGRAINE ( 9 FDA reports)
PARAESTHESIA ( 9 FDA reports)
PYREXIA ( 9 FDA reports)
VIRAL INFECTION ( 9 FDA reports)
WEIGHT DECREASED ( 9 FDA reports)
ADNEXA UTERI CYST ( 8 FDA reports)
DYSMENORRHOEA ( 8 FDA reports)
DYSPAREUNIA ( 8 FDA reports)
HYPEREMESIS GRAVIDARUM ( 8 FDA reports)
MYOCARDIAL INFARCTION ( 8 FDA reports)
VAGINITIS BACTERIAL ( 8 FDA reports)
VIRAL UPPER RESPIRATORY TRACT INFECTION ( 8 FDA reports)
DEPRESSED MOOD ( 6 FDA reports)
DEPRESSION ( 6 FDA reports)
TREMOR ( 6 FDA reports)
ANAEMIA ( 5 FDA reports)
BRONCHOSPASM ( 5 FDA reports)
ESCHERICHIA TEST POSITIVE ( 5 FDA reports)
FATIGUE ( 5 FDA reports)
MENORRHAGIA ( 5 FDA reports)
PELVIC PAIN ( 5 FDA reports)
PREGNANCY ( 5 FDA reports)
SOMNOLENCE ( 5 FDA reports)
UTERINE HAEMORRHAGE ( 5 FDA reports)
CHEST PAIN ( 4 FDA reports)
CHILLS ( 4 FDA reports)
CONTUSION ( 4 FDA reports)
CULTURE URINE POSITIVE ( 4 FDA reports)
DRUG INTERACTION ( 4 FDA reports)
NAUSEA ( 4 FDA reports)
PAIN ( 4 FDA reports)
SKIN FLAP NECROSIS ( 4 FDA reports)
STATUS MIGRAINOSUS ( 4 FDA reports)
SUICIDAL IDEATION ( 4 FDA reports)
AGITATION ( 3 FDA reports)
APHONIA ( 3 FDA reports)
CONFUSIONAL STATE ( 3 FDA reports)
COUGH ( 3 FDA reports)
DELIRIUM ( 3 FDA reports)
DRUG EXPOSURE DURING PREGNANCY ( 3 FDA reports)
FEBRILE NEUTROPENIA ( 3 FDA reports)
GAIT DISTURBANCE ( 3 FDA reports)
HYPOAESTHESIA ( 3 FDA reports)
HYPOVOLAEMIA ( 3 FDA reports)
LIVER FUNCTION TEST ABNORMAL ( 3 FDA reports)
LOSS OF CONSCIOUSNESS ( 3 FDA reports)
MANIA ( 3 FDA reports)
MENSTRUATION DELAYED ( 3 FDA reports)
MOOD ALTERED ( 3 FDA reports)
MUSCULAR WEAKNESS ( 3 FDA reports)
MYALGIA ( 3 FDA reports)
REFUSAL OF TREATMENT BY PATIENT ( 3 FDA reports)
RENAL FAILURE ACUTE ( 3 FDA reports)
SYNCOPE ( 3 FDA reports)
TOOTH DISCOLOURATION ( 3 FDA reports)
URINARY INCONTINENCE ( 3 FDA reports)
VAGINAL HAEMORRHAGE ( 3 FDA reports)
VOMITING ( 3 FDA reports)
ABDOMINAL PAIN ( 2 FDA reports)
ACCIDENTAL DEATH ( 2 FDA reports)
APPENDICECTOMY ( 2 FDA reports)
ASTHENIA ( 2 FDA reports)
BLOOD PRESSURE DECREASED ( 2 FDA reports)
COLONIC POLYP ( 2 FDA reports)
CONVULSION ( 2 FDA reports)
DEEP VEIN THROMBOSIS ( 2 FDA reports)
DIABETIC RETINOPATHY ( 2 FDA reports)
DIARRHOEA ( 2 FDA reports)
DRUG ABUSE ( 2 FDA reports)
DRUG LEVEL BELOW THERAPEUTIC ( 2 FDA reports)
DRUG TOXICITY ( 2 FDA reports)
DYSPHONIA ( 2 FDA reports)
ESCHERICHIA INFECTION ( 2 FDA reports)
EYE PAIN ( 2 FDA reports)
FEELING COLD ( 2 FDA reports)
HAEMODIALYSIS ( 2 FDA reports)
HAEMOGLOBIN DECREASED ( 2 FDA reports)
HYPOKALAEMIA ( 2 FDA reports)
INCORRECT DOSE ADMINISTERED ( 2 FDA reports)
LABYRINTHITIS ( 2 FDA reports)
MALAISE ( 2 FDA reports)
MATERNAL EXPOSURE DURING PREGNANCY ( 2 FDA reports)
MELAENA ( 2 FDA reports)
MEMORY IMPAIRMENT ( 2 FDA reports)
MUSCULOSKELETAL PAIN ( 2 FDA reports)
NO ADVERSE EVENT ( 2 FDA reports)
PERITONEAL NEOPLASM ( 2 FDA reports)
PHARMACEUTICAL PRODUCT COMPLAINT ( 2 FDA reports)
PNEUMONIA ( 2 FDA reports)
PROTEINURIA ( 2 FDA reports)
PRURITUS ( 2 FDA reports)
PSEUDOMONAS INFECTION ( 2 FDA reports)
RENAL IMPAIRMENT ( 2 FDA reports)
RETINAL DISORDER ( 2 FDA reports)
RHABDOMYOLYSIS ( 2 FDA reports)
RHINITIS ALLERGIC ( 2 FDA reports)
ROTATOR CUFF SYNDROME ( 2 FDA reports)
SEBORRHOEIC KERATOSIS ( 2 FDA reports)
STREPTOCOCCAL INFECTION ( 2 FDA reports)
TENDONITIS ( 2 FDA reports)
THINKING ABNORMAL ( 2 FDA reports)
ABDOMINAL MASS ( 1 FDA reports)
ACUTE PSYCHOSIS ( 1 FDA reports)
AMENORRHOEA ( 1 FDA reports)
AMNESIA ( 1 FDA reports)
ANXIETY ( 1 FDA reports)
ARTHRALGIA ( 1 FDA reports)
BACK PAIN ( 1 FDA reports)
BASAL CELL CARCINOMA ( 1 FDA reports)
BLISTER ( 1 FDA reports)
BLOOD CHLORIDE INCREASED ( 1 FDA reports)
BLOOD GLUCOSE INCREASED ( 1 FDA reports)
BODY HEIGHT DECREASED ( 1 FDA reports)
CHROMATURIA ( 1 FDA reports)
CHRONIC OBSTRUCTIVE PULMONARY DISEASE ( 1 FDA reports)
DEVICE MALFUNCTION ( 1 FDA reports)
DISCOMFORT ( 1 FDA reports)
DRUG DOSE OMISSION ( 1 FDA reports)
DRUG EFFECT DECREASED ( 1 FDA reports)
DRUG INEFFECTIVE ( 1 FDA reports)
DYSPHAGIA ( 1 FDA reports)
DYSPHORIA ( 1 FDA reports)
ECTOPIC PREGNANCY ( 1 FDA reports)
ERECTILE DYSFUNCTION ( 1 FDA reports)
ESCHERICHIA URINARY TRACT INFECTION ( 1 FDA reports)
FALL ( 1 FDA reports)
FLANK PAIN ( 1 FDA reports)
FLUSHING ( 1 FDA reports)
FUNGAL INFECTION ( 1 FDA reports)
GASTROENTERITIS NOROVIRUS ( 1 FDA reports)
GASTROOESOPHAGEAL REFLUX DISEASE ( 1 FDA reports)
HAEMATOCRIT DECREASED ( 1 FDA reports)
HAEMORRHAGE ( 1 FDA reports)
HERNIA ( 1 FDA reports)
INADEQUATE ANALGESIA ( 1 FDA reports)
INJECTION SITE PAIN ( 1 FDA reports)
INJECTION SITE RASH ( 1 FDA reports)
INTESTINAL POLYP ( 1 FDA reports)
LETHARGY ( 1 FDA reports)
LOWER RESPIRATORY TRACT INFECTION ( 1 FDA reports)
LUNG INFILTRATION ( 1 FDA reports)
MENSTRUATION IRREGULAR ( 1 FDA reports)
MENTAL STATUS CHANGES ( 1 FDA reports)
NEPHROLITHIASIS ( 1 FDA reports)
NERVOUSNESS ( 1 FDA reports)
NODULE ( 1 FDA reports)
OESOPHAGITIS ( 1 FDA reports)
PAIN IN EXTREMITY ( 1 FDA reports)
PALPITATIONS ( 1 FDA reports)
PREGNANCY WITH CONTRACEPTIVE DEVICE ( 1 FDA reports)
PRODUCT QUALITY ISSUE ( 1 FDA reports)
RASH ( 1 FDA reports)
RED BLOOD CELL COUNT DECREASED ( 1 FDA reports)
RED CELL DISTRIBUTION WIDTH INCREASED ( 1 FDA reports)
RETICULOCYTE COUNT INCREASED ( 1 FDA reports)
RETINAL HAEMORRHAGE ( 1 FDA reports)
ROCKY MOUNTAIN SPOTTED FEVER ( 1 FDA reports)
SHOCK ( 1 FDA reports)
SINUS CONGESTION ( 1 FDA reports)
SKIN BURNING SENSATION ( 1 FDA reports)
SWOLLEN TONGUE ( 1 FDA reports)
TARDIVE DYSKINESIA ( 1 FDA reports)
URINE FLOW DECREASED ( 1 FDA reports)
VISUAL DISTURBANCE ( 1 FDA reports)
WITHDRAWAL SYNDROME ( 1 FDA reports)
WRONG TECHNIQUE IN DRUG USAGE PROCESS ( 1 FDA reports)

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