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

PULMONARY EMBOLISM ( 19 FDA reports)
CHEST PAIN ( 11 FDA reports)
CHOLELITHIASIS ( 11 FDA reports)
NAUSEA ( 11 FDA reports)
CHOLECYSTITIS CHRONIC ( 10 FDA reports)
DEEP VEIN THROMBOSIS ( 10 FDA reports)
DIZZINESS ( 10 FDA reports)
INJURY ( 10 FDA reports)
LOSS OF CONSCIOUSNESS ( 10 FDA reports)
PAIN IN EXTREMITY ( 10 FDA reports)
PALPITATIONS ( 10 FDA reports)
VOMITING ( 10 FDA reports)
ANXIETY ( 9 FDA reports)
DYSPNOEA ( 9 FDA reports)
PAIN ( 9 FDA reports)
BACK PAIN ( 8 FDA reports)
CONDITION AGGRAVATED ( 8 FDA reports)
GALLBLADDER DISORDER ( 8 FDA reports)
VAGINITIS BACTERIAL ( 8 FDA reports)
ABDOMINAL PAIN UPPER ( 7 FDA reports)
CYSTITIS ( 7 FDA reports)
HYPERTENSION ( 7 FDA reports)
OEDEMA PERIPHERAL ( 7 FDA reports)
VULVOVAGINAL MYCOTIC INFECTION ( 7 FDA reports)
CONVULSION ( 6 FDA reports)
DYSMENORRHOEA ( 6 FDA reports)
HAEMODYNAMIC INSTABILITY ( 6 FDA reports)
HYPERHIDROSIS ( 6 FDA reports)
HYPOKALAEMIA ( 6 FDA reports)
PREMATURE RUPTURE OF MEMBRANES ( 6 FDA reports)
RETAINED PLACENTA OR MEMBRANES ( 6 FDA reports)
SEASONAL ALLERGY ( 6 FDA reports)
ALOPECIA ( 5 FDA reports)
BILIARY COLIC ( 5 FDA reports)
CEREBROVASCULAR ACCIDENT ( 5 FDA reports)
DIARRHOEA ( 5 FDA reports)
FALL ( 5 FDA reports)
FATIGUE ( 5 FDA reports)
HEADACHE ( 5 FDA reports)
HYPERLIPIDAEMIA ( 5 FDA reports)
INSOMNIA ( 5 FDA reports)
LEFT VENTRICULAR HYPERTROPHY ( 5 FDA reports)
SYNCOPE ( 5 FDA reports)
URINARY TRACT INFECTION ( 5 FDA reports)
ARRHYTHMIA ( 4 FDA reports)
ARTHRALGIA ( 4 FDA reports)
ASTHENIA ( 4 FDA reports)
BLOOD CHOLESTEROL INCREASED ( 4 FDA reports)
BRONCHIAL HYPERREACTIVITY ( 4 FDA reports)
CHOLECYSTITIS ACUTE ( 4 FDA reports)
DEMYELINATION ( 4 FDA reports)
DEPRESSION ( 4 FDA reports)
DIABETES MELLITUS ( 4 FDA reports)
DRUG INEFFECTIVE ( 4 FDA reports)
EMOTIONAL DISTRESS ( 4 FDA reports)
GLYCOSYLATED HAEMOGLOBIN INCREASED ( 4 FDA reports)
HYPERCOAGULATION ( 4 FDA reports)
INTERNATIONAL NORMALISED RATIO INCREASED ( 4 FDA reports)
INTRA-UTERINE DEATH ( 4 FDA reports)
IRON DEFICIENCY ANAEMIA ( 4 FDA reports)
LOW DENSITY LIPOPROTEIN INCREASED ( 4 FDA reports)
MIGRAINE ( 4 FDA reports)
NEUROPATHY PERIPHERAL ( 4 FDA reports)
TREMOR ( 4 FDA reports)
VENTRICULAR EXTRASYSTOLES ( 4 FDA reports)
VERTIGO ( 4 FDA reports)
WOUND SEPSIS ( 4 FDA reports)
ABDOMINAL PAIN LOWER ( 3 FDA reports)
ANHEDONIA ( 3 FDA reports)
BACTERAEMIA ( 3 FDA reports)
BREAST MASS ( 3 FDA reports)
BURNING SENSATION ( 3 FDA reports)
CERVICAL INCOMPETENCE ( 3 FDA reports)
CHOLECYSTECTOMY ( 3 FDA reports)
DRUG EXPOSURE DURING PREGNANCY ( 3 FDA reports)
DYSFUNCTIONAL UTERINE BLEEDING ( 3 FDA reports)
FEELING ABNORMAL ( 3 FDA reports)
HAEMATOCHEZIA ( 3 FDA reports)
HYPERCHOLESTEROLAEMIA ( 3 FDA reports)
HYPERVENTILATION ( 3 FDA reports)
MENORRHAGIA ( 3 FDA reports)
MULTIPLE SCLEROSIS ( 3 FDA reports)
NECK PAIN ( 3 FDA reports)
OVARIAN CYST ( 3 FDA reports)
PARAESTHESIA ( 3 FDA reports)
PHARMACEUTICAL PRODUCT COMPLAINT ( 3 FDA reports)
PREGNANCY ( 3 FDA reports)
PRODUCTIVE COUGH ( 3 FDA reports)
PYREXIA ( 3 FDA reports)
RHINITIS ALLERGIC ( 3 FDA reports)
RIGHT VENTRICULAR HYPERTROPHY ( 3 FDA reports)
ROAD TRAFFIC ACCIDENT ( 3 FDA reports)
SINUS TACHYCARDIA ( 3 FDA reports)
STAPHYLOCOCCAL SEPSIS ( 3 FDA reports)
TYPE 2 DIABETES MELLITUS ( 3 FDA reports)
ABDOMINAL DISCOMFORT ( 2 FDA reports)
ABDOMINAL PAIN ( 2 FDA reports)
ABSCESS ( 2 FDA reports)
AMENORRHOEA ( 2 FDA reports)
ANAPHYLACTIC REACTION ( 2 FDA reports)
ANORECTAL DISCOMFORT ( 2 FDA reports)
BLOOD GLUCOSE DECREASED ( 2 FDA reports)
BLOOD PRESSURE DECREASED ( 2 FDA reports)
BLOOD PRESSURE SYSTOLIC DECREASED ( 2 FDA reports)
CARDIAC ENZYMES INCREASED ( 2 FDA reports)
CARDIOMYOPATHY ( 2 FDA reports)
CERVICAL DYSPLASIA ( 2 FDA reports)
CERVICITIS ( 2 FDA reports)
CERVIX CARCINOMA ( 2 FDA reports)
CHOLESTEROSIS ( 2 FDA reports)
CIRCULATORY COLLAPSE ( 2 FDA reports)
CONTUSION ( 2 FDA reports)
CYST ( 2 FDA reports)
DRUG ABUSER ( 2 FDA reports)
DRUG DEPENDENCE ( 2 FDA reports)
DRUG WITHDRAWAL SYNDROME ( 2 FDA reports)
EMOTIONAL DISORDER ( 2 FDA reports)
EXTRASYSTOLES ( 2 FDA reports)
GASTROOESOPHAGEAL REFLUX DISEASE ( 2 FDA reports)
GENERAL PHYSICAL HEALTH DETERIORATION ( 2 FDA reports)
GENITAL HAEMORRHAGE ( 2 FDA reports)
GRAND MAL CONVULSION ( 2 FDA reports)
HAEMATURIA ( 2 FDA reports)
HAIR DISORDER ( 2 FDA reports)
HEART INJURY ( 2 FDA reports)
HEART RATE DECREASED ( 2 FDA reports)
HYPOAESTHESIA ( 2 FDA reports)
HYPOTENSION ( 2 FDA reports)
INADEQUATE ANALGESIA ( 2 FDA reports)
IRRITABILITY ( 2 FDA reports)
JOINT SWELLING ( 2 FDA reports)
LACUNAR INFARCTION ( 2 FDA reports)
LUMBAR RADICULOPATHY ( 2 FDA reports)
MADAROSIS ( 2 FDA reports)
MALAISE ( 2 FDA reports)
MYDRIASIS ( 2 FDA reports)
NASAL OBSTRUCTION ( 2 FDA reports)
NEPHROLITHIASIS ( 2 FDA reports)
OPTIC NERVE DISORDER ( 2 FDA reports)
ORGAN FAILURE ( 2 FDA reports)
PALLOR ( 2 FDA reports)
PELVIC PAIN ( 2 FDA reports)
POST PROCEDURAL COMPLICATION ( 2 FDA reports)
POST PROCEDURAL DISCOMFORT ( 2 FDA reports)
POST PROCEDURAL INFECTION ( 2 FDA reports)
POST-TRAUMATIC STRESS DISORDER ( 2 FDA reports)
PRESYNCOPE ( 2 FDA reports)
PROCEDURAL DIZZINESS ( 2 FDA reports)
PROCEDURAL PAIN ( 2 FDA reports)
PROCTALGIA ( 2 FDA reports)
PROTHROMBIN TIME PROLONGED ( 2 FDA reports)
PRURITUS GENERALISED ( 2 FDA reports)
RETCHING ( 2 FDA reports)
SINUSITIS ( 2 FDA reports)
SKIN IRRITATION ( 2 FDA reports)
TENDERNESS ( 2 FDA reports)
THROAT TIGHTNESS ( 2 FDA reports)
THROMBOSIS ( 2 FDA reports)
UPPER RESPIRATORY TRACT INFECTION ( 2 FDA reports)
UTERINE LEIOMYOMA ( 2 FDA reports)
UTERINE SPASM ( 2 FDA reports)
VAGINAL DISCHARGE ( 2 FDA reports)
VAGINAL INFECTION ( 2 FDA reports)
VENTRICULAR HYPERTROPHY ( 2 FDA reports)
WHITE BLOOD CELL COUNT DECREASED ( 2 FDA reports)
ABDOMINAL DISTENSION ( 1 FDA reports)
ABORTION SPONTANEOUS ( 1 FDA reports)
AFFECT LABILITY ( 1 FDA reports)
AGGRESSION ( 1 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 1 FDA reports)
AMNIOTIC FLUID VOLUME DECREASED ( 1 FDA reports)
ANTIBIOTIC RESISTANT STAPHYLOCOCCUS TEST POSITIVE ( 1 FDA reports)
ANTIBODY TEST POSITIVE ( 1 FDA reports)
ANTINUCLEAR ANTIBODY POSITIVE ( 1 FDA reports)
ANTITHROMBIN III DEFICIENCY ( 1 FDA reports)
AORTIC VALVE INCOMPETENCE ( 1 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 1 FDA reports)
ASTHMA ( 1 FDA reports)
AURA ( 1 FDA reports)
BILIARY DYSKINESIA ( 1 FDA reports)
BURSITIS ( 1 FDA reports)
CARPAL TUNNEL SYNDROME ( 1 FDA reports)
CHOLECYSTITIS ( 1 FDA reports)
CHORIOAMNIONITIS ( 1 FDA reports)
CLAUSTROPHOBIA ( 1 FDA reports)
CONSTIPATION ( 1 FDA reports)
DEFORMITY ( 1 FDA reports)
DEHYDRATION ( 1 FDA reports)
DIABETES MELLITUS INADEQUATE CONTROL ( 1 FDA reports)
DISTURBANCE IN ATTENTION ( 1 FDA reports)
DRUG EXPOSURE BEFORE PREGNANCY ( 1 FDA reports)
DYSLIPIDAEMIA ( 1 FDA reports)
DYSPEPSIA ( 1 FDA reports)
EARLY SATIETY ( 1 FDA reports)
ELECTROCARDIOGRAM ST SEGMENT DEPRESSION ( 1 FDA reports)
ENTHESOPATHY ( 1 FDA reports)
EPSTEIN-BARR VIRUS TEST POSITIVE ( 1 FDA reports)
ESSENTIAL HYPERTENSION ( 1 FDA reports)
FACTOR III DEFICIENCY ( 1 FDA reports)
FACTOR V DEFICIENCY ( 1 FDA reports)
FIBROMYALGIA ( 1 FDA reports)
FLATULENCE ( 1 FDA reports)
FLUID OVERLOAD ( 1 FDA reports)
FOETAL DISORDER ( 1 FDA reports)
HAEMORRHOIDAL HAEMORRHAGE ( 1 FDA reports)
HALLUCINATION, AUDITORY ( 1 FDA reports)
HEAD INJURY ( 1 FDA reports)
HYPERTHYROIDISM ( 1 FDA reports)
HYPOTHYROIDISM ( 1 FDA reports)
IMMOBILE ( 1 FDA reports)
INCISION SITE INFECTION ( 1 FDA reports)
INCONTINENCE ( 1 FDA reports)
INFUSION SITE PHLEBITIS ( 1 FDA reports)
INJECTION SITE PHLEBITIS ( 1 FDA reports)
INTERNAL INJURY ( 1 FDA reports)
LIGAMENT SPRAIN ( 1 FDA reports)
LYME DISEASE ( 1 FDA reports)
MATERNAL EXPOSURE DURING PREGNANCY ( 1 FDA reports)
METRORRHAGIA ( 1 FDA reports)
MITRAL VALVE INCOMPETENCE ( 1 FDA reports)
MOBILITY DECREASED ( 1 FDA reports)
MYOCARDIAL INFARCTION ( 1 FDA reports)
MYOMECTOMY ( 1 FDA reports)
NO ADVERSE EVENT ( 1 FDA reports)
NOCTURNAL DYSPNOEA ( 1 FDA reports)
NUCLEAR MAGNETIC RESONANCE IMAGING BRAIN ABNORMAL ( 1 FDA reports)
OEDEMA ( 1 FDA reports)
OFF LABEL USE ( 1 FDA reports)
ORAL DISORDER ( 1 FDA reports)
OSTEOARTHRITIS ( 1 FDA reports)
OVARIAN CYSTECTOMY ( 1 FDA reports)
PHLEBITIS ( 1 FDA reports)
PIRIFORMIS SYNDROME ( 1 FDA reports)
PLATELET COUNT DECREASED ( 1 FDA reports)
PREGNANCY WITH CONTRACEPTIVE DEVICE ( 1 FDA reports)
PREGNANCY WITH IMPLANT CONTRACEPTIVE ( 1 FDA reports)
PREMATURE BABY ( 1 FDA reports)
PREMATURE LABOUR ( 1 FDA reports)
PRODUCT SUBSTITUTION ISSUE ( 1 FDA reports)
PROTEIN C DEFICIENCY ( 1 FDA reports)
PROTEIN S INCREASED ( 1 FDA reports)
PROTEINURIA ( 1 FDA reports)
PRURITUS ( 1 FDA reports)
PULMONARY OEDEMA ( 1 FDA reports)
QRS AXIS ABNORMAL ( 1 FDA reports)
RASH ( 1 FDA reports)
RASH GENERALISED ( 1 FDA reports)
RASH PRURITIC ( 1 FDA reports)
RECTAL HAEMORRHAGE ( 1 FDA reports)
RED BLOOD CELL COUNT DECREASED ( 1 FDA reports)
RENAL FAILURE ( 1 FDA reports)
RENAL TUBULAR NECROSIS ( 1 FDA reports)
RHINITIS SEASONAL ( 1 FDA reports)
SCAR ( 1 FDA reports)
SNORING ( 1 FDA reports)
SOMNOLENCE ( 1 FDA reports)
STAPHYLOCOCCAL INFECTION ( 1 FDA reports)
SUICIDE ATTEMPT ( 1 FDA reports)
SWELLING ( 1 FDA reports)
TENSION HEADACHE ( 1 FDA reports)
THERAPEUTIC RESPONSE DECREASED ( 1 FDA reports)
THERAPEUTIC RESPONSE UNEXPECTED WITH DRUG SUBSTITUTION ( 1 FDA reports)
TREATMENT FAILURE ( 1 FDA reports)
TREATMENT NONCOMPLIANCE ( 1 FDA reports)
TRICUSPID VALVE INCOMPETENCE ( 1 FDA reports)
VASCULITIS ( 1 FDA reports)
VENTRICULAR TACHYCARDIA ( 1 FDA reports)
VULVOVAGINITIS ( 1 FDA reports)
WOUND INFECTION STAPHYLOCOCCAL ( 1 FDA reports)

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